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Senior

NOT
High School

General Biology 2
Quarter 1 - Module 1
GENETICS

GENERAL BIOLOGY 2
Department of Education ● Republic of the Philippines

1
Earth Science- Grade 12
Alternative Delivery Mode
Quarter 1 - Module 1: Genetics
First Edition, 2020

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Published by the Department of Education – Division of Cagayan de Oro Schools
Division Superintendent: Dr. Cherry Mae L. Limbaco, CESO V
Development Team of the Module

Author:

Reviewers: Jean S. Macasero, Shirley Merida, Duque Caguindangan, Eleanor Rollan,


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Langam, Amelito Bucod

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Chairperson: Cherry Mae L. Limbaco, Ph.D., CESO V
Schools Division Superintendent

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2
Senior High School
Senior High School

General Biology
2
Quarter 1 - Module 1:
Genetics

This instructional material was collaboratively developed and reviewed


by educators from public and private schools, colleges, and or/universities. We
encourage teachers and other education stakeholders to email their feedback,
comments, and recommendations to the Department of Education at action@
deped.gov.ph.

We value your feedback and recommendations.

Department of Education ● Republic of the Philippines

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Table of Contents

What This Module is About ...................................................................................................................i


What I Need to Know..............................................................................................................................ii
How to Learn from this Module ...........................................................................................................ii
Icons of this Module ...............................................................................................................................iii

What I Know........................................................................................................................................... iii

First Quarter
Lesson 1: Genetic Engineering
What I Need to Know..................................................................................................13
What’s I Know: Definition of Terms.........................................................................13
What New.......................................................................................................................13
What is It: Leaning Concepts………………………………………………………14-15

What’s More: Poster Making………………………………………………………….16


What’s I’ve learned: Determining Genetic Technology…. ................................16 What I Can

Do: Pros and Cons ...............................................................................16 Lesson 2:


Applications of Recombinant DNA

What I Need to Know..................................................................................................17


What’s I Know: Definition of Terms.........................................................................17

What’s New: Designer Genes ..................................................................................17

What’s Is It: Learning Concepts …………………………………………………..16-20

What’s More: ...............................................................................................................20


What I’ve Learned………………………………….........................................21
Lesson 3: History of Life on Earth

What I Need to Know..................................................................................................22


What I Know: Definition of Terms............................................................................22

What’s New:..................................................................................................................22

What is It: Learning Concepts…………………………………………………….23-25

What I Have Learned: ………………………………………………………………25-26


Lesson 4: Mechanisms that Produce Change in Populations
What I Need to Know..................................................................................................27

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What I know: Definition of Terms ............................................................................27

What’s New: A Picture Paint a Thousand Words................................................27

What is It: Learning Concept………………………………………………….28-30

Lesson 5: Evolution and Origin of Biodiversity: Patterns


of Descent with Modification

What I Need to Know..................................................................................................31


What I Know: Definition of Terms............................................................................31

What’s New...................................................................................................................31

What is It: Learning Concepts……………………………………………………….32-33

What’s More .................................................................................................................33


What I’ve Learned:.....................................................................................33-34
Lesson 6: Development of EvolutionaryThought

What I Need to Know..................................................................................................35


What’s New: .................................................................................................................35

What Is It: Learning Concepts..................................................................................35

What’s More: Charles Darwin Journey………………………………………….36-37

What I Have Learned: ...............................................................................................38


Lesson 7: Evidences of Evolution

What I Need to Know..................................................................................................39


What’s New: .................................................................................................................39

What Is It: Learning Concepts..................................................................................40

What’s More: Evolution Evidences……………………………………………….41-42


Lesson 8: Evolutionary Relationships of Organisms

What I Need to Know..................................................................................................43


What I Know: Definition of Terms............................................................................43

What’s New: Family Features ..................................................................................43

What is It: Learning Concepts…………………………………………………….44-45


What’s More: Phylogenic Tree.................................................................................46
What I Can Do: …………………………………….........................................46

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Lesson 9: Systematics Based on Evolutionary
Relationships: Tree of Life and Systematics
What I Need to Know..................................................................................................47
What I Know: Definition of Terms............................................................................47

What’s New: Similarities and Uniqueness ............................................................47

What is It: Learning Concept……………………………………………….48-49

What’s More: Essay....................................................................................................50

Lesson 10: Systematics Based on Evolutionary Relationships:


Taxonomy
What I Need to Know..................................................................................................51
What I Know: Definition of Terms............................................................................51

What’s New:..................................................................................................................51

What is It: Learning Concepts ..................................................................................52

What’s More: Practical Uses of Biological Classification ..................................53

Lesson 11: Systematics Based on Evolutionary Relationships:


Cladistics and Phylogeny
What I Need to Know..................................................................................................54
What I Know: Definition of Terms............................................................................54

What’s New...................................................................................................................54

What Is It: Learning Concept....................................................................................55

What’s More: Phylogenic Tree.................................................................................55


What I Can Do: …………………………………….........................................55

References ............................................................................................................................................ 56
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Module 1
Genetics
What This Module is About

This module demonstrates your understanding of the characteristics of Earth


that are necessary to support life, particularly on the essential components of this
planet that drives all living things or biotic factors (plants, animals, microorganisms) to
exist. It also emphasizes on the different subsystems (geosphere, hydrosphere,
atmosphere, and biosphere) that make up the Earth and how these systems interact
to produce the kind of Earth we live in today.

This module will help you explore the key concepts on topics that will help you
answer the questions pertaining to our very own, planet earth.

This module has eleven (11) lessons:


• Lesson 1: Genetic Engineering
• Lesson 2: Applications of Recombinant DNA
• Lesson 3: History of Life on Earth
• Lesson 4: Mechanisms that Produce Change in Populations • Lesson 5:
Evolution and Origin of Biodiversity: Patterns of Descent with Modification
• Lesson 6: Development of Evolutionary Thought
• Lesson 7: Evidences of Evolution
• Lesson 8: Evolutionary Relationships of OrganismsLesson 9:
Systematics Based on Evolutionary Relationships: Tree of Life and
Systematics
• Lesson 10: Systematics Based on Evolutionary Relationships:
Taxonomy
• Lesson 11: Systematics Based on Evolutionary Relationships:
Cladistics and Phylogeny

What I Need to Know


After going through this module, you are expected to:
1. Outline the processes involved in genetic engineering. (STEM_BIO11/12-IIIa-b-6) 2.
Discuss the applications of recombinant DNA. (STEM_BIO11/12-IIIa-b-7) 3. Describe
general features of the history of life on Earth, including generally accepted
dates and sequence of the geologic time scale and characteristics of major groups of
organisms present during these time periods. (STEM_BIO11/12-IIIc-g-8) 4. Explain the
mechanisms that produce change in populations from generation to generation (e.g.,
artificial selection, natural selection, genetic drift, mutation, recombination)
(STEM_BIO11/12-IIIc-g-9)
5. Show patterns of descent with modification from
6. Common ancestors to produce the organismal diversity observed today.
STEM_BIO11/12-IIIc-g-10
7. Trace the development of evolutionary thought (STEM_BIO11/12-IIIc-g-11)

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8. Explain evidences of evolution (e.g., biogeography, fossil record, DNA/protein
sequences, homology, and embryology) (STEM_BIO11/12-IIIc-g-12) 9. Infer evolutionary
relationships among organisms using the evidence of evolution.
(STEM_BIO11/12-IIIc-g-13)
10. Explain how the structural and developmental characteristics and relatedness of DNA
sequences are used in classifying living things. STEM_BIO11/12IIIhj-14 11. Identify the
unique/ distinctive characteristics of a specific taxon relative to other taxa
(STEM_BIO11/12IIIhj-15)
12. Describe species diversity and cladistics, including the types of evidence and
procedures that can be used to establish evolutionary relationships.
(STEM_BIO11/12IIIhj-16)
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How to Learn from this Module

To achieve the learning competencies cited above, you are to do the following:
• Take your time reading the lessons carefully.
• Follow the directions and/or instructions in the activities and exercises diligently. •
Answer all the given tests and exercises.
Icons of this Module
What I Need This part contains learning objectives
to Know that are set for you to learn as you go
along the module.

What I know This is an assessment as to your level


of knowledge to the subject matter at
hand, meant specifically to gauge
prior related knowledge

What’s In This part connects previous lesson with


that of the current one.

What’s New An introduction of the new lesson


through various activities, before it will be
presented to you

What is It These are discussions of the activities


as a way to deepen your discovery and
under standing of the concept.
What’s More These are follow-up activities that are in
tended for you to practice further in order
to master the competencies.

What I Have Activities designed to process what


Learned you have learned from the lesson

What I can do These are tasks that are designed to


show case your skills and knowledge
gained, and applied into real-life concerns
and situations.

II

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1Genetic Engineering
Lesson

What I need to know


Learning Competency
The learners should be able to outline the steps involved in genetic engineering
(STEM_BIO11/12-III a-b-6)

At the end of the lesson, the learners will be able to:


• compare classical breeding with modern genetic engineering techniques;
• enumerate the steps in molecular cloning;
• describe some methods to introduce DNA into cells; and
• explain the selection and screening of transformants / genetically modified
organisms (GMOs)

What I know
Definition of Terms:

1. Genetic Engineering 6. Genome


2. DNA 7. Gene Mapping
3. Recombinant DNA 8. Biotechnology
4. Plasmids 9. Polymerase Chain Reaction
5. Cloning 10. Gene Therapy

What’s new
PRE-ACTIVITY:

1.How organisms may be modified?


2. Enumerate plants and animals that have desirable or enhanced traits and how each of the traits
was introduced or developed. Modifying Technique ex. Classical Breeding, Recombinant DNA
Technology.
ENHANCED TRAIT MODIFYING TECHNIQUE
Example: Flavr-Savr (Delayed Ripening Recombinant DNA Technology
Tomatoes

1. 1.

2. 2.

3. 3.

4. 4.

5. 5.

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What’s is it
INTRODUCTION:

❖ Genetic engineering, the artificial manipulation, modification, and recombination of DNA or


other nucleic acid molecules in order to modify an organism or population of organisms. ❖ The
term genetic engineering initially referred to various techniques used for the modification
or manipulation of organisms through the processes of heredity and reproduction. As such,
the term embraced both artificial selection and all the interventions of biomedical
techniques, among them artificial insemination, in vitro fertilization (e.g., “test-tube” babies),
cloning, and gene manipulation.
https://www.britannica.com/science/genetic-engineering

❖ Classical plant breeding uses deliberate interbreeding (crossing) of closely or distantly related
individuals to produce new crop varieties or lines with desirable properties. Plants are
crossbred to introduce traits/genes from one variety or line into a new genetic background.
https://www.sciencedaily.com/terms/plant_breeding.htm#:~:text=Classical%20plant%20breeding%20uses%20deliberate,i
nto%20a%20new%20genetic%20background.

❖ Genetic engineering is the process of using recombinant DNA (rDNA) technology to alter the
genetic makeup of an organism. Traditionally, humans have manipulated genomes indirectly
by controlling breeding and selecting offspring with desired traits. Genetic engineering
involves the direct manipulation of one or more genes. Most often, a gene from another
species is added to an organism's genome to give it a desired phenotype.
https://www.genome.gov/genetics-glossary/Genetic
Engineering#:~:text=Genetic%20engineering%20is%20the%20process,selecting%20offspring%20with%20desired%20traits.

Genetic engineering involves the use of molecular techniques to modify the traits of a target
organism. The modification of traits may involve:
1. introduction of new traits into an organism
2. enhancement of a present trait by increasing the expression of the desired gene 3.
enhancement of a present trait by disrupting the inhibition of the desired genes’ expression. A
general outline of recombinant DNA may be given as follows:
1. cutting or cleavage of DNA by restriction enzymes (REs)
2. selection of an appropriate vector or vehicle which would propagate the recombinant DNA (
eg. circular plasmid in bacteria with a foreign gene of interest)
3. ligation (join together) of the gene of interest (eg. from animal) with the vector (cut bacterial
plasmid)
4. transfer of the recombinant plasmid into a host cell (that would carry out replication to make
huge copies of the recombined plasmid)
5. selection process to screen which cells actually contain the gene of interest
6. sequencing of the gene to find out the primary structure of the protein
Ways in which these plasmids may be introduced into host organisms:
❖ Biolistics. In this technique, a “gene gun” is used to fire DNA-coated pellets on plant tissues.
Cells that survive the bombardment, and are able to take up the expression plasmid coated
pellets and acquire the ability to express the designed protein.

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❖ Plasmid insertion by Heat Shock Treatment. Heat Shock Treatment is a process used to
transfer plasmid DNA into bacteria. The target cells are pre-treated before the procedure to
increase the pore sizes of their plasma membranes. This pretreatment (usually with CaCl2) is
said to make the cells “competent” for accepting the plasmid DNA. After the cells are made
competent, they are incubated with the desired plasmid at about 4°C for about 30min. The
plasmids concentrate near the cells during this time. Afterwards, a “Heat Shock” is done on
the plasmid-cell solution by incubating it at 42°C for 1 minute then back to 4°C for 2 minutes.
The rapid rise and drop of temperature is believed to increase and decrease the pore sizes in
the membrane. The plasmid DNA near the membrane surface are taken into the cells by this
process. The cells that took up the plasmids acquire new traits and are said to be
“transformed”.
❖ Electroporation. This technique follows a similar methodology as Heat Shock Treatment, but,
the expansion of the membrane pores is done through an electric “shock”. This method is
commonly used for insertion of genes into mammalian cells.
Some methods are:
• Selection of plasmid DNA containing cells
• Selection of transformed cells with the desired gene
• PCR detection of plasmid DNA
• Genetically Modified Organisms (GMOs)

What’s more
Poster Making:

Create a poster on the steps and other methods involved in recombinant DNA.

What’s I’ve learned


POST QUIZ:

1. Determine which technologies are most appropriate for which cell types.
TECHNOLOGY CELL TYPE
1 Plants cells

2. Electroporation

3.Biolistics

4. Bacterial cells

5. Mammalian cells

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What’s I can do
PERFORMANCE TASK:

1. Research on the pros and cons of genetic engineering.


PROS CONS

1.

2.

3.

4.

5.

2. What is your opinion on Genetic Engineering? Note: Support your opinion with facts and include
the issue of biosafety.

RECOMMENDED READINGS:

1. https://www.ck12.org/book/human-biology-genetics/section/10.1/
2.https://www.ck12.org/c/biology/biotechnology/lesson/Biotechnology
BIO/?referrer=concept_details
3.https://www.khanacademy.org/science/biology/biotech-dna-technology/intro-to-biotech
tutorial/a/intro-to-biotechnology
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Discuss the Applications of


2
Lesson
Recombinant DNA

What I need to know


Learning Competency:
The learners should be able to discuss the applications of Recombinant DNA
Technology (STEM_BIO11/12-III a-b-7)

Specific Learning Outcomes:


At the end of the lesson, the learners will be able to:
• give examples of products from recombinant DNA technology;
• illustrate the use of databases to search genes for desired traits;
• describe steps in PCR to amplify and detect a gene of interest;
• identify the parts of an expression vector;
• explain how genes may be cloned and expressed

What I know
PRIOR KNOWLEDGE: Definition of Terms

1. Clone 6. Modified Trait


2. Plasmids 7. Human Genome
3. Biotechnology 8. Genetic Modified Organism
4. PCR Amplification
5. Detection

What’s new
PRE-ACTIVITY: Designer Genes Work
1. How does DNA Replicate?
2. What is Genetically Modified Organism (GMO)?
3. Illustrate your own Designer genes based on the following:
1. Identify a special trait.
2. Identify a source organism.
3. Identify a target organism.
4. Identify the modified/ added trait.
Example: Hot Tomato > Chili > Tomato > Spicy Tomato

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Tomatoes

It was reported this week that Brazilian scientists are hoping to create spicy tomatoes using Crispr
gene-editing techniques. Although tomatoes contain the genes for capsaicinoids (the chemicals that
give chillies their heat) they are dormant – Crispr could be used to make them active. This is desirable
because, compared to tomatoes, chillies are difficult to farm – and capsaicinoids have other useful
applications besides their flavour – in pepper spray for example.
https://www.theguardian.com/science/2019/jan/13/the-five-genetically-modified-fruit-edited-bananas-tomatoes

What’s is it
INTRODUCTION:

PRESENTATION OF RECOMBINANT DNA

There are many different traits that can be introduced to organisms to change their properties. The
following table shows examples of modified traits using cloned genes and their applications:
MODIFIED TRAIT GENE MODIFICATION RECIPIENT ORGANISM APPLICATION (FIELD)
Insulin Production Insertion of Bacteria (Medicine)
Human Insulin Production of
Gene Human Insulin in
Bacteria

Pest Resistance Insertion of Bt-toxin Corn / Maize (Agriculture)


gene Production of corn
plants with
increased
resistance to corn
boxer

Delayed Ripening Disruption of a Tomato plant Agriculture)


gene for a ripening Production of
enzyme (e.g. plants with fruits
polygalacturonase) that have delayed
ripening
fruits. These fruits
will survive longer
transport time,
allowing their
delivery to further
locations (i.e.
export deliveries)

Chymosin Production Insertion of a gene Bacteria (Industry)


for chymosin Enhance large
scale production
of
chymosin. This
enzyme
serves as a
substitute for
rennet in the
coagulation of
milk. Rennet has
to be
harvested from
calves. The large
scale
production of this
enzyme in bacteria
provides an
abundant supply of
this
important component

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for the cheese
production industry.

❖ PCR Amplification
Once a desired trait is chosen, information must be acquired for either its detection or expression in a
given organism.

1. Detection
❖ Some researchers may be interested in determining if a given gene/trait is available in a
particular organism. If no previous research provides this information, researchers may test
the DNA of different organisms for the presence of these specific genes. A technique that
allows the detection of specific genes in target organisms is called PCR.
❖ PCR amplification is an in-vitro method that simulates DNA replication in vivo. It utilizes a
thermostable (heat-resistant) DNA polymerase that builds single stranded DNA strands unto
unwound DNA templates.
❖ PCR uses repeated cycles of incubation at different temperatures to promote the unwinding of
the DNA template (~95°C); the annealing of a primer (a ~20bp oligonucleotide sequence
(recall RNA primers in DNA replication) onto the ssDNA template strand (~54 - 60°C); and the
extension of the generated ssDNA strand through the binding of complementary bases to the
template strand (~72° C). The thermostability of the polymerase allows it to survive the
repeated cycles of denaturation, annealing and extension with little loss of enzyme function.
Each cycle of PCR doubles the amount of the target sequence. A typical PCR experiment uses
about 35 cycles of amplification. This increases the original amount of the target sequence by
235 (i.e. ~34 billion) times.
❖ Gene detection by PCR involves the design of primers that would only bind to sequences that
are specific to a target. For example, researchers would want to find out if gene X (e.g. the
gene for insulin) is available in a target organism (e.g. a mouse, Mus musculus). Primers may
be designed by looking at the available sequences for gene X in the databases (e.g. all the
genes for insulin in different organisms; humans, pigs, cows, etc.). The different gene X
sequences must be aligned/ compared to match areas of sequence similarity (conserved
sequences) and areas of sequence dissimilarity (non-conserved sequences). Primers designed
to have the same sequence as the conserved areas will be specific for binding gene X
sequences in all the target organisms. Primers designed to have the same sequence as the
non-conserved areas will only be specific for the organisms which match its sequence.
STEPS in PCR Amplification

❖ Step 0: Undenatured Template ; Temp ~ 54 °"C;


Template: double stranded (ds) DNA strand. Complementary sequences are held together by H-bonds
5’ A T GCGATGAGGATATGACCCGATAGATAGAGGTATCTAGAGAT 3’ (Coding strand) 3’ T A
CGCTACTCCTATACTGGGCTATCTATCTCCATAGATCTCTA 5’ (Non-coding strand)

❖ Step 1: Template denaturation ; Temp ~ 95 °"C;


Template: single stranded (ss) DNA strands; DNA strands are separated; H-bonds between
complementary sequences are broken
5’ A T GCGATGAGGATATGACCCGATAGATAGAGGTATCTAGAGAT 3’ (Coding strand) 3’ T A
CGCTACTCCTATACTGGGCTATCTATCTCCATAGATCTCTA 5’ (Non-coding strand) ❖ Step 2: Primer
Annealing ; Temp ~ 54 °"C (dependent on primer melting temperature); Template: ssDNA strands.
H-bonds are formed between complementary sequences on the primers and the target sequences.
5’ A T GCGATGAGGATATGACCCGATAGATAGAGGTATCTAGAGAT 3’ (Coding strand)
Direction of elongation 🡨 CCATAGATC (Reverse Primer)

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5’ GCGATGAGG 3’ → Direction of elongation (Forward Primer)

3’ T A CGCTACTCCTATACTGGGCTATCTATCTCCATAGATCTCTA 5’ (Non-coding strand) ❖


Step 3: New DNA strand elongation ; Temp ~ 72 °"C;
The two new dsDNA strands are formed by the elongation of the generated ssDNA and the H-bonds
between the complementary sequences on these new strands and their templates. Each of the new
dsDNA strands is made up of one old strand from the original template, and one new strand that was
generated as a reverse complement of the template. This is called semiconservative replication of the
sequence.

New Strand 1:
5’ A T GCGATGAGGATATGACCCGATAGATAGAGGTATCTAGAGAT 3’ (Coding strand) (old) 3’
CGCTACTCCTATACTGGGCTATCTATCTCCATAGATC-5’ (Reverse Primer) (new)

New Strand 2:
5’ GCGATGAGGATATGACCCGATAGATAGAGGTATCTAG-3’ (Forward Primer) (new) 3’ T A
CGCTACTCCTATACTGGGCTATCTATCTCCATAGATCTCTA 5’ (Non-coding strand) (old)

❖ Step 4: Repeat step 1 to 3 for N number of cycles (N is usually 35)


PCR Results
The expected product of PCR amplification will depend on the sequences / position at which the
primer sequences bind. If the forward primer starts binding at nucleotide 3 (coming from the 5’ end)
of
a 43bp long gene, and the reverse primer binds at a position complementary to nucleotide 39 of the
coding strand, then a 37bp product is expected per cycle of PCR.

PCR Applications

❖ PCR may be used to detect the presence of a desired gene in an organism. Depending on the
primer design, the expected product may represent only a specific region of the gene or the
entire gene itself. The first case is useful for detection of the gene, or the detection of
organisms with that specific gene within a sample. The second case is useful for the
amplification of the entire gene for eventual expression in other organisms. The direct
amplification/copying of a full gene is part of the process for “cloning” that gene.
2. Cloning and Expression
❖ Some genes provide economically, and industrially important products (e.g. insulin-coding
genes; genes for collagen degradation). In some cases, scientists would want to put these
genes into organisms for the expression of their products. One example would be the
insertion of an insulin- coding gene from the human genome into bacteria. This allows the
“transformed” bacteria to now produce human insulin as a product.
❖ Certain types of bacteria are capable of this process since they are able to take genes within
their cell membranes for eventual expression. The genes are normally in the form of small,
circular DNA structures called plasmids.

What’s more
ACTIVITY:

1. Illustrate the steps in restriction digestion and PCR.

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What’s I’ve
learnedPOST QUIZ:
1. Discuss how PCR may be used for the detection of disease-causing pathogens in a population
during the COVID Pandemic.
For example: it may be used to check if a patient has a COVID virus infection. 2. Discuss how the
cloning and expression of certain genes allows for massive production of the desired product.
For Example: the cloning and expression of insulin in bacteria allows for the mass
production of this necessary protein for use by diabetic patients.

RECOMMENDED READINGS:

1.https://flexbooks.ck12.org/cbook/ck-12-middle-school-life-science
2.0/section/3.18/primary/lesson/recombinant-dna-ms-ls
2. https://www.ck12.org/book/cbse_biology_book_class_xii/section/14.1/
3. https://www.ck12.org/section/dna-technology/

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History of Life on Earth
3

Lesson

What I need to know


Learning Competency
The learners describe general features of the history of life on Earth, including generally accepted
dates and sequence of the geologic time scale and characteristics (STEM_BIO11/12-IIIc-g-8)

Specific Learning Outcomes


At the end of the lesson, the learners will be able to:
• identify the dates and sequence of the periods in the geologic time scale;
• identify the major events in each major period;
• describe the characteristics of the major groups of organisms’ presents during a time
period; • identify types of fossils; and
• describe causes of mass extinctions.

What I know
PRIOR KNOWLEDGE: Definition of Terms

1. Precambrian 6. Cambrian 11. Permian


2. Paleozoic 7. Ordovician 12. Triassic
3. Mesozoic 8. Silurian 13. Jurassic
4. Cenozoic 9. Devonian 14. Cretaceous
5. Epoch 10. Carboniferous

What’s new
PRE-ACTIVITY:

1. What is the age of the Earth?


2. What was the Earth like million years ago? Describe.
3. Watch a video clip on YouTube. Geological Time Scale and Fossils
(https://www.youtube.com/watch?v=3EfewdEC8bk)
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What’s is it
INTRODUCTION:
https://clarkscience8.weebly.com/geologic-time-scale.html

The Geological Time Scale (GTS)


A. Four eras - Precambrian; Paleozoic; Mesozoic; Cenozoic

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B. Periods under the Paleozoic era - Cambrian, Ordovician, Silurian, Devonian, Carboniferous,
Permian
C. Periods under the Mesozoic era - Triassic, Jurassic, Cretaceous
D. Periods under the Cenozoic era - Tertiary and Quaternary

CAMBRIAN EXPLOSION is the belief that there was a sudden, apparent explosion of diversity in life
forms about 545 million years ago. The explosion created the complexity of multi-celled organisms in
a relatively short time frame of 5 to 10 million years. This explosion also created most of the major
extant animal groups today.
TYPES OF FOSSILS DESCRIPTION EXAMPLES

Molds Impression made in a Shells


substrate = negative image
of an organism

Casts When a mold is filled in Bones and teeth

Petrified Organic material is Petrified trees;


converted into stone Coal balls (fossilized plants
and their tissues, in round
ball shape)

Original Remains Preserved wholly (frozen in Woolly mammoth;


ice, trapped in tar pits, Amber from the Baltic
dried/ dessicated inside Sea region
caves in arid regions or
encased in amber/
fossilized resin)

Carbon Film Carbon impression in Leaf impression on the rock


sedimentary rocks

Trace/ Ichnofossils Record the movements Trackways, toothmarks,


and behaviors of the gizzard rocks, coprolites
organism (fossilized dungs), burrows
and nests

THE SIX WAYS OF FOSSILIZATION


1. Unaltered preservation - Small organism or part trapped in amber, hardened plant sap 2.
Permineralization/ Petrification - The organic contents of bone and wood are replaced with
silica, calcite or pyrite, forming a rock-like fossil
3. Replacement - hard parts are dissolved and replaced by other minerals, like calcite, silica,
pyrite, or iron
4. Carbonization or Coalification - The other elements are removed and only the carbon
remained
5. Recrystalization - Hard parts are converted to more stable minerals or small crystals turn into
larger crystals
6. Authigenic preservation - Molds and casts are formed after most of the organism have been
7. destroyed or dissolved
DATING FOSSILS

Knowing the age of a fossil can help a scientist establish its position in the geologic time scale and find
its relationship with the other fossils. There are two ways to measure the age of a fossil: relative
dating and absolute dating.

1. RELATIVE DATING
• Based upon the study of layer of rocks
• Does not tell the exact age: only compare fossils as older or younger, depends on their position
in rock layer
24
• Fossils in the uppermost rock layer/ strata are younger while those in the lowermost deposition
are oldest
How Relative Age is Determined
• Law of Superposition: if a layer of rock is undisturbed, the fossils found on upper layers are
younger than those found in lower layers of rocks
• However, because the Earth is active, rocks move and may disturb the layer making this process
not highly accurate
Rules of Relative Dating
(From: http://staff.harrisonburg.k12.va.us/~esutliff/forms/Relative_Dating_1334236393.ppt)

A. LAW OF SUPERPOSITION: Sedimentary layers are deposited in a specific time- youngest rocks on
top, oldest rocks at the bottom
B. LAW OF ORIGINAL HORIZONTALITY: Deposition of rocks happen horizontally- tilting, folding or
breaking happened recently

C. LAW OF CROSS-CUTTING RELATIONSHIPS: If an igneous intrusion or a fault cuts through existing


rocks, the intrusion/fault is YOUNGER than the rock it cuts through
INDEX FOSSILS (guide fossils/ indicator fossils/ zone fossils): fossils from short-lived organisms that
lived in many places; used to define and identify geologic periods

2. ABSOLUTE DATING
• Determines the actual age of the fossil
• Through radiometric dating, using radioactive isotopes carbon-14 and potassium-40 •
Considers the half-life or the time it takes for half of the atoms of the radioactive element to
decay
• The decay products of radioactive isotopes is stable atoms.

What’s I’ve learned


MULTIPLE CHOICE. Choose the letter of the correct answer.

1. The largest division of the geologic time scale is the


A. Eon
B. Era
C. Period
D. Epoch

2. The Mesozoic Era was the Age of Reptiles while the current
Cenozoic Era is the Age of
A. Mammals
B. Birds
C. Humans
D. Technology

3. The layers in sedimentary rocks are also called


A. eras
B. epochs
C. strata
D. gaps

25
4. The movie “Jurassic Park” got its title from which era?
A. Paleozoic
B. Mesozoic
C. Cenozoic
D. Holozoic

5. During which era were the first land plants formed?


A. Cambrian
B. Pre-Cambrian
C. Paleozoic
D. Mesozoic

6. The era of middle life, a time of many changes on Earth


A. Paleozoic
B. Mesozoic
C. Cenozoic
D. Holozoic

7. What is the longest part of Earth’s history where trace fossils


appeared.
A. Pre-Cambrian
B. Paloezoic
C. Mesozoic
D. Cenozoic

8. The geologic time scale is subdivided into 4 groups. List them


from the largest to the smallest.
A. Eons, periods, epochs, eras
B. Eras, eons, periods, epochs
C. Epochs, periods, eras, eons
D. Eons, eras, periods, epochs

9. The end of this era was believed to be caused by a comet or


asteroid colliding with Earth, causing a huge cloud of dust and
smoke to rise into the atmosphere, blocking out the sun.
A. Paleozoic
B. Holozoic
C. Mesozoic
D. Cenozoic

10. Which geologic event occurred during the Mesozoic era?


A. Pangaea formed
B. Asteroids killed the dinosaurs
C. The Rocky Mountains formed
D. The Pleistocene Ice Age began

RECOMMENDED READINGS

1.https://flexbooks.ck12.org/cbook/ck-12-middle-school-life-science
2.0/section/4.13/primary/lesson/timeline-of-evolution-ms-ls/
2.https://flexbooks.ck12.org/cbook/ck-12-middle-school-earth-science-flexbook
2.0/section/15.7/primary/lesson/geologic-time-scale-ms-es/
3.https://www.ck12.org/book/ck-12-earth-science-concepts-for-high-school/section/10.7/

26

Mechanisms that Produce


4
Lesson
Change in Populations

a
What I need to know

Learning Competency
The learners shall be able to explain the mechanisms that produce change in populations from
generation to generation (STEM_BIO11/12-IIIc-g-9)

Specific Learning Outcomes

At the end of the lesson, the learners will be able to:


• explain that genetic variation is the prerequisite and should therefore be present for any genetic
process to cause change in populations from generation to generation;
• state the Hardy-Weinberg Principle;
• enumerate the conditions that should be present for a gene or in a larger scale, a population, to
attain Hardy-Weinberg equilibrium; and
• calculate gene and genotype frequencies and derive the Hardy-Weinbergequation

What I know

PRIOR KNOWLEDGE:

1. Natural Selection 6. Genetic Variation


2. Mitigation 7. DNA Sequence
3. Mutation 8. Genetic Drift
4. Genotype
5. Genetic Equilibrium
27

What’s new
PRE ACTIVITY: A Picture Paint a Thousand Words

1. Observe the two pictures and Recognize the


similarities and the differences between individuals or
animals belonging to the same species.

https://www.dogalize.com/2016/12/dog-breeds/
https://blogs.scientificamerican.com/observations/the-concept-of-race-is-a-lie/

What’s is it
INTRODUCTION:

❖ Hardy–Weinberg law The law that states that in an infinitely large, interbreeding population in
which mating is random and in which there is no selection, migration, or mutation, gene and
genotype frequencies will remain constant from generation to generation. In practice these
conditions are rarely strictly present, but unless any departure is a marked one, there is no
statistically significant movement away from equilibrium. Consider a single pair of alleles, A
and a, present in a diploid population with frequencies of p and q respectively. Three
genotypes are possible, AA, Aa, and aa, and these will be present with frequencies of p2, 2pq,
and q2 respectively.
https://www.encyclopedia.com/science-and-technology/biology-and-genetics/genetics-and-genetic
engineering/hardy-weinberg
law#:~:text=Hardy%E2%80%93Weinberg%20law%20The%20law,generation%2C%20with%20no%20overlap%20b
etween
❖ The five conditions that must be met for genetic equilibrium to occur include:

1. No mutation (change) in the DNA sequence.


2. No migration (moving into or out of a population).
3. A very large population size.
4. Random mating.
5. No natural selection.
https://www.ck12.org/book/ck-12-life-science-concepts-for-middle-school/section/4.9/

28
❖ The Hardy-Weinberg equation is a mathematical equation that can be used to calculate the
genetic variation of a population at equilibrium. he equation is an expression of the principle
known as Hardy-Weinberg equilibrium, which states that the amount of genetic variation in a
population will remain constant from one generation to the next in the absence of disturbing
factors.
p2 + 2pq + q2 = 1

where p is the frequency of the "A" allele and q is the frequency of the "a" allele in the population. In
the equation, p2 represents the frequency of the homozygous genotype AA, q2 represents the
frequency of the homozygous genotype aa, and 2pq represents the frequency of the heterozygous
genotype Aa. In addition, the sum of the allele frequencies for all the alleles at the locus must be 1, so
p + q = 1. If the p and q allele frequencies are known, then the frequencies of the three genotypes
may be calculated using the Hardy-Weinberg equation.

https://www.nature.com/scitable/definition/hardy-weinberg-equation-299/#:~:text=Science%20at%20Scitable-
,Hardy%2DWeinberg%20equation,In%201908%2C%20G.%20H.&text=If%20the%20p%20and%20q,using%20the%20Hardy%
2DWeinberg%20equation.

❖ Natural selection, genetic drift, and gene flow are the mechanisms that cause changes in allele
frequencies over time. When one or more of these forces are acting in a population, the
population violates the Hardy-Weinberg assumptions, and evolution occurs.
❖ Natural selection occurs when individuals with certain genotypes are more likely than
individuals with other genotypes to survive and reproduce, and thus to pass on their alleles to
the next generation. As Charles Darwin (1859) argued in On the Origin of Species, if the
following conditions are met, natural selection must occur:

1. There is variation among individuals within a population in some trait.


2. This variation is heritable (i.e., there is a genetic basis to the variation, such that offspring
tend to resemble their parents in this trait).
3. Variation in this trait is associated with variation in fitness (the average net reproduction of
individuals with a given genotype relative to that of individuals with other genotypes).

❖ Mutation. Although mutation is the original source of all genetic variation, mutation rate for
most organisms is pretty low. So, the impact of brand-new mutations on allele frequencies from
one
generation
to the next
is usually
not large.
(However,
natural
selection
acting on
the results
of a mutation can be a powerful mechanism of

evolution!)
❖ Natural selection. Finally, the most famous mechanism of evolution! Natural selection occurs
when one allele (or combination of alleles of different genes) makes an organism more or less
fit, that is, able to survive and reproduce in a given environment. If an allele reduces fitness,
its frequency will tend to drop from one generation to the next. We will look in detail at
different forms of natural selection that occur in populations.

29

❖ Gene
flow. Gene flow involves the movement of genes into or out of a population, due to
either the movement of individual organisms or their gametes (eggs and sperm, e.g., through
pollen dispersal by a plant). Organisms and gametes that enter a population may have new
alleles, or may bring in existing alleles but in different proportions than those already in the
population. Gene flow can be a strong agent of evolution.


Non-infinite population size (genetic drift). Genetic drift involves changes in allele frequency
due to chance events – literally, "sampling error" in selecting alleles for the next generation.
Drift can occur in any population of non-infinite size, but it has a stronger effect on small
populations. We will look in detail at genetic drift and the effects of population size.
https://www.khanacademy.org/science/biology/her/heredity-and-genetics/a/hardy-weinberg-mechanisms-of-evolution

30
Biodiversity: Patterns
Lesson 5 of Descent with
Evolution and Origin of Modification

What I need to know


Learning Competency
The learners shall be able to show patterns of descent with modification from common ancestors to
produce the organismal diversity observed today.
STEM_BIO11/12-IIIc-g-10

Specific Learning Outcomes


At the end of the lesson, the learners will be able to:
• define species according to the biological species concept;
• distinguish the various types of reproductive isolating mechanisms that can lead to speciation;
• discuss the different modes of speciation; and
• explain how evolution produce the tremendous amount of diversity among organisms.

What I know

PRIOR KNOWLEDGE: Definition of Terms

1. Species 6. Allopatric
2. Classification 7. Sympatric
3. Interbreeding 8. Parapatric
4. Isolating mechanism
5. Zygote
What’s new
PRE ACTIVITY: Answer the following questions briefly.

1. Identify or give an organism which can be an animal or a plant species.


2. Identify the different kind or variants of the species.
Example:
Specie: Cat
Kinds or Variants: Lion, Tiger, Cheetah

31

What’s is it
INTRODUCTION:

❖ Species, in biology, classification comprising related organisms that share common


characteristics and are capable of interbreeding.
https://www.britannica.com/science/species-taxon
❖ Ernst Mayer’s definition: “Species are groups of interbreeding natural populations that are
reproductively isolated from other such groups.”

The reproductive isolating mechanisms

A. Pre-zygotic isolation mechanisms prevent fertilization and zygote formation. I. geographic or


ecological or habitat isolation – potential mates occupy different areas or habitats thus, they
never come in contact
II. temporal or seasonal isolation – different groups may not be reproductively mature at the
same season, or month or year
III. behavioral isolation – patterns of courtship are different
IV. mechanical isolation – differences in reproductive organs prevent successful interbreeding
V. gametic isolation – incompatibilities between egg and sperm prevent fertilization B.
Post-zygotic isolation mechanisms allow fertilization but nonviable or weak or sterile hybrids are
formed.
I. hybrid inviability – fertilized egg fails to develop past the early embryonic stages II. hybrid
sterility – hybrids are sterile because gonads develop abnormally or there is abnormal
segregation of chromosomes during meiosis
III. hybrid breakdown - F1 hybrids are normal, vigorous and viable, but F2 contains many weak or
sterile individuals
The modes of speciation:
A. Allopatric speciation or geographic speciation (allo – other, patric – place; ‘other place’) -
occurs when some members of a population become geographically separated from the
other members thereby preventing gene flow. Examples of geographic barriers are bodies of
water and mountain ranges.
B. Sympatric speciation (sym – same, patric – place; ‘same place’) - occurs when members of a
population that initially occupy the same habitat within the same range diverge into two or
more different species. It involves abrupt genetic changes that quickly lead to the
reproductive isolation of a group of individuals. Example is change in chromosome number
(polyploidization).
C. Parapatric speciation (para – beside, patric – place; ‘beside each other’) – occurs when the
groups that evolved to be separate species are geographic neighbors. Gene flow occurs but
with great distances is reduced. There is also abrupt change in the environment over a
geographic border and strong disruptive selection must also happen.

32

What’s more
ACTIVITY:

1. Research 5 similar species with different characteristics.


Example: Gartner snakes live in the same region One lives in water

One lives in land


What’s I’ve learned
POST QUIZ:

1. Give examples on the reproductive isolating mechanisms.


MECHANISMS EXAMPLES

1. Geographic Isolation 1.
2.
3.

2. Temporal or Seasonal Isolation 1.


2.

33
3

3. Behavioral Isolation 1.
2.
3

4. Mechanical Isolation 1.
2.
3

5. Gametic Isolation 1.
2.
3

Recommended Readings:
1. https://www.khanacademy.org/science/biology/her/tree-of-life/a/species-speciation
34

Development of Evolutionary
6
Lesson
Thought
What I need to know
Learning Competency
The learners shall be able to trace the development of evolutionary thought. STEM_BIO11/12-IIIc-g
11

Specific Learning Outcomes


At the end of the lesson, the learners will be able to:
• enumerate the scientists and cite their respective contributions in the development of evolutionary
thought;
• describe Jean Baptiste Lamarck’s hypothesis on evolutionary change;
• discuss Charles Darwin’s theory of evolution by natural selection; and
• explain the Modern Synthesis as the unified theory of evolution

What I know
PRIOR KNOWLEDGE: Definition of Terms

1. Taxonomy 6. Family
2. Kingdom 7. Genus
3. Phylum 8. Species
4. Class 9.Natural Selection
5. Order 10. Artificial Selection

What’s new
PRE-ACTIVITY: Research

1. Create a “Photo Collage” about Evolution.


2. Enumerate the scientist and cite their respective contributions in the development of evolutionary
thought.
SCIENTIST CONTRIBUTIONS

1.
2.
3.

35
4.
5.
What’s is it
INTRODUCTION:

❖ Scientific classification is a method by which biologists organize living things into groups. It is
also called taxonomy. Groups of organisms in taxonomy are called taxa (singular, taxon). You
may already be familiar with commonly used taxa, such as the kingdom and species.
❖ Why do biologists classify organisms? The major reason is to make sense of the incredible
diversity of life on Earth. Scientists have identified millions of different species of organisms.
Among animals, the most diverse group of organisms is the insects.
Linnaean System of Classification

❖ The most influential early classification system was developed by Carolus Linnaeus. In fact, all
modern classification systems have their roots in Linnaeus’ system. Linnaeus was a Swedish
botanist who lived during the 1700s. He is known as the “father of taxonomy.” Linnaeus tried
to describe and classify the entire known natural world. In 1735, he published his
classification system in a work called Systema Naturae (“System of Nature”).
❖ The taxa are below:
o Kingdom - This is the highest taxon in Linnaean taxonomy, representing major
divisions of organisms. Kingdoms of organisms include the plant and animal kingdoms. o
Phylum (plural, phyla) - This taxon is a division of a kingdom. Phyla in the animal kingdom
include chordates (animals with an internal skeleton) and arthropods (animals with an
external skeleton).
o Class - This taxon is a division of a phylum. Classes in the chordate phylum include
mammals and birds.
o Order - This taxon is a division of a class. Orders in the mammal class include rodents
and primates.
o Family - This taxon is a division of an order. Families in the primate order include
hominids (apes and humans) and hylobatids (gibbons).
o Genus - This taxon is a division of a family. Genera in the hominid family include Homo
(humans) and Pan (chimpanzees).
o Species - This taxon is below the genus and the lowest taxon in Linnaeus’ system.
Species in the Pan genus include Pan troglodytes(common chimpanzees) and Pan
paniscus (pygmy chimpanzees).
https://www.ck12.org/book/cbse_biology_book_class_xi/section/1.3/

36
❖ Thomas Malthus was an English economist. He wrote a popular essay called “On Population.”
He argued that human populations have the potential to grow faster than the resources they
need. When populations get too big, disease and famine occur. These calamities control
population size by killing off the weakest people.
❖ Catastrophism was a theory developed by Georges Cuvier based on paleontological evidence
in the Paris Basin. Cuvier was there when he observed something peculiar about the fossil
record. Instead of finding a continuous succession of fossils, Cuvier noticed several gaps
where all evidence of life would disappear and then abruptly reappear again after a notable
amount of time. Cuvier recognized these gaps in the fossil succession as mass extinction
events.
❖ This led Cuvier to develop a theory called catastrophism. Catastrophism states that natural
history has been punctuated by catastrophic events that altered that way life developed and
rocks were deposited.
❖ In geology, gradualism is a theory developed by James Hutton according to which profound
changes to the Earth
❖ This theory inspired an evolution theory in paleontology, also called gradualism, according to
which the species appeared by the gradual transformation of ancestral species. ❖ According to
this theory, the population of a species is transformed slowly and progressively into a new
species by the accumulation of micro-evolutionary changes in the genetic heritage. ❖ The law of
use and disuse, which states that when certain organs become specially developed as a result of
some environmental need, then that state of development is hereditary and can be passed on to
progeny.
Evolution of Darwin’s Theory

❖ It took Darwin years to form his theory of evolution by natural selection. His reasoning went
like this:
1. Like Lamarck, Darwin assumed that species can change over time. The fossils he
found helped convince him of that.
2. From Lyell, Darwin saw that Earth and its life were very old. Thus, there had been
enough time for evolution to produce the great diversity of life Darwin had observed. 3. From
Malthus, Darwin knew that populations could grow faster than their resources. This
“overproduction of offspring” led to a “struggle for existence,” in Darwin’s words.
4. From artificial selection, Darwin knew that some offspring have variations that
occur by chance, and that can be inherited. In nature, offspring with certain variations might
be more likely to survive the “struggle for existence” and reproduce. If so, they would pass
their favorable variations to their offspring.
5. Darwin coined the term fitness to refer to an organism’s relative ability to survive
and produce fertile offspring. Nature selects the variations that are most useful. Therefore,
he called this type of selection natural selection.
6. Darwin knew artificial selection could change domestic species over time. He
inferred that natural selection could also change species over time. In fact, he thought that if
a species changed enough, it might evolve into a new species.

37

What’s more
ACTIVITY:
Answer the following questions on a separate sheet of paper:
a. What did Darwin’s travels reveal to him about the number and variety of living species?
b. How did tortoises and birds differ among the islands of the Galapagos?
c. What is evolution? Why is referred to as a theory?
d. Darwin found fossils of many organisms that were different from any living species. How
would this finding has affecting his understanding of lifes diversity?

What’s I’ve learned


POST QUIZ:

Write true if the statement is true or false if the statement is false.


_____ 1. As recently as 200 years ago, many people believed that Earth was only 6,000 years old.
_____ 2. Artificial selection occurs when nature selects for beneficial traits.
_____ 3. The individual Galápagos Islands are all similar to each other.
_____ 4. Malthus argued that human populations grow faster than their resources. _____ 5.
Lamarck was one of the first scientists to propose that species evolve by natural selection. _____ 6.
Lyell was one of the first to say that Earth must be far older than most people believed. _____ 7.
Lamarck’s inheritance of acquired characteristics is has become a widely accepted scientific theory.
_____ 8. Fossils proved to Darwin that species can evolve.
_____ 9. The term fitness to refer to an organism’s ability to outrun its hunters. _____ 10. Darwin
published his findings soon after returning to England from the voyage of the Beagle. _____ 11.
According to Darwin, natural selection is what occurs, and evolution is how it happens. _____ 12.
During his journey aboard the Beagle, Darwin found fossils from the seas in the mountains. _____ 13.
Galápagos tortoises have differently shaped shells depending on where they live. _____ 14. Darwin’s
book changed science forever.
_____ 15. Alfred Russel Wallace developed a theory of evolution at the same time as Darwin.

38
Evidences of Evolution
7

Lesson

What I need to know


Learning Competency
The learners explain evidences of evolution (e.g. fossil record, biogeography, DNA/ protein sequences,
homology and embryology (STEM_BIO11/12-IIIc
g-12)

Specific Learning Outcomes


At the end of the lesson, the learners will be able to:
• describe the evidences to support evolution and
• explain some modern evidences of evolution

What I know
PRIOR KNOWLEDGE: Definition of Terms

1. Homologous 6. Genetic code


2. Analogous 7. Biogeography
3. Molecular Biology 8. Fossils
4. Transcription 9. Evolution
5. Translation 10. Modification

What’s new
PRE-ACTIVITY: Video

1. List down 5 evidences of evolution.


2. Fossils & Evidence for Evolution: https://www.youtube.com/watch?v=iYr3sYS9e0w
39

What’s is it
INTRODUCTION:

❖ The Evidence for Evolution Anatomy and embryology Darwin thought of evolution as "descent
with modification," a process in which species change and give rise to new species over many
generations. He proposed that the evolutionary history of life forms a branching tree with
many levels, in which all species can be traced back to an ancient common ancestor.
❖ Homologous features If two or more species share a unique physical feature, such as a
complex bone structure or a body plan, they may all have inherited this feature from a
common ancestor. Physical features shared due to evolutionary history (a common ancestor)
are said to be homologous.
❖ Analogous features To make things a little more interesting and complicated, not all physical
features that look alike are marks of common ancestry. Instead, some physical similarities are
analogous: they evolved independently in different organisms because the organisms lived in
similar environments or experienced similar selective pressures. This process is called
convergent evolution. (To converge means to come together, like two lines meeting at a
point.)
❖ Determining relationships from similar features In general, biologists don't draw conclusions
about how species are related on the basis of any single feature they think is homologous.
Instead, they study a large collection of features (often, both physical features and DNA
sequences) and draw conclusions about relatedness based on these features as a group. We
will explore this idea further when we examine phylogenetic trees.
❖ Molecular biology Like structural homologies, similarities between biological molecules can
reflect shared evolutionary ancestry. At the most basic level, all living organisms share: ❖ The
same genetic material (DNA)
❖ The same, or highly similar, genetic codes
❖ The same basic process of gene expression (transcription and translation)
❖ The same molecular building blocks, such as amino acids
❖ Biogeography The geographic distribution of organisms on Earth follows patterns that are
best explained by evolution, in combination with the movement of tectonic plates over
geological time.
❖ Fossil record Fossils are the preserved remains of previously living organisms or their traces,
dating from the distant past. The fossil record is not, alas, complete or unbroken: most
organisms never fossilize, and even the organisms that do fossilize are rarely found by
humans.
40

What’s
moreACTIVITY:
Identify the evidence shown by the picture and explain how it supports evolution.
41
42

Evolutionary Relationships of
8
Lesson
Organisms

What I need to know


Learning Competency
The learners should be able to infer evolutionary relationships among organisms using the evidences
of evolution (STEM_BIO11/12-IIIc-g-13)

Specific Learning Outcomes


At the end of the lesson, the learners will be able to:
• recognize how comparisons of similarities and differences can suggest evolutionary relationships; •
explain the significance of using multiple lines of evidence to identify evolutionary relationships; •
infer the degree of relationships among organisms based on the amino acid sequence in the
cytochrome c molecule;
• compare four species of horses by measuring structures in their hind legs;
and • differentiate various hominids by describing their physical features.

What I know
PRIOR KNOWLEDGE: Definition of Terms

1. Phylogeny 6. Polytomy
2. Phylogenetic Tree 7. Taxonomy
3. Branch Point 8. Binomial Nomenclature
4. Basal Taxon
5. Sister Taxa

What’s new
PRE-ACTIVITY:

1. Recall and Write the evidences of Evolution.

43

What’s is it
INTRODUCTION:
INFERRING RELATIONSHIPS FROM EVIDENCES OF EVOLUTION
Living things share some biomolecules which may be used to prove relationships. These chemicals
include DNA and proteins. The building blocks of these chemicals may be analyzed to show
similarities and differences among organisms. The more similarities, the closer the relationships.

One of these is the protein cytochrome-c, an important enzyme found in virtually all organisms. It is a
highly conserved protein which functions in the electron transport chain system of the mitochondria
which is needed for the release of energy from food. It also performs a role in apoptosis
(programmed cell death) by being released into the cytosol activating the events of cell death.

There are 104 amino acids in the human cytochrome c, 37 of which have been found at the same
position in every cytochrome c that has been sequenced. The molecules are assumed to have
descended from a primitive microbial cytochrome that existed over two billion years ago.

A cladogram is a diagram used to represent a hypothetical relationship between groups of animals,


called a phylogeny. A cladogram is used by a scientist studying phylogenetic systematics to visualize
the groups of organisms being compared, how they are related, and their most common ancestors.

A phylogeny is a hypothetical relationship between groups of organisms being compared. A


phylogeny is often depicted using a phylogenetic tree.

A phylogenetic tree is a diagram used to reflect evolutionary relationships among organisms or groups
of organisms. Scientists consider phylogenetic trees to be a hypothesis of the evolutionary past since
one cannot go back to confirm the proposed relationships. In other words, a “tree of life” can be
constructed to illustrate when different organisms evolved and to show the relationships among
different organisms

a phylogenetic tree can be read like a map of evolutionary history. Many phylogenetic trees have a
single lineage at the base representing a common ancestor.

Scientists call such trees rooted, which means there is a single ancestral lineage (typically drawn from
the bottom or left) to which all organisms represented in the diagram relate. Notice in the rooted
phylogenetic tree that the three domains— Bacteria, Archaea, and Eukarya—diverge from a single
point and branch off. The small branch that plants and animals (including humans) occupy in this

44
diagram shows how recent and miniscule these groups are compared with other organisms.
Unrooted trees don’t show a common ancestor but do show relationships among species.

In a rooted tree, the branching indicates evolutionary relationships (Figure 3). The point where a split
occurs, called a branch point, represents where a single lineage evolved into a distinct new one. A
lineage that evolved early from the root and remains unbranched is called basal taxon. When two
lineages stem from the same branch point, they are called sister taxa. A branch with more than two
lineages is called a polytomy and serves to illustrate where scientists have not definitively determined
all of the relationships. It is important to note that although sister taxa and polytomy do share an
ancestor, it does not mean that the groups of organisms split or evolved from each other. Organisms
in two taxa may have split apart at a specific branch point, but neither taxa gave rise to the other.
https://courses.lumenlearning.com/suny-wmopen-biology2/chapter/phylogenies-and-the-history
of
life/#:~:text=In%20scientific%20terms%2C%20the%20evolutionary,closely%20related%2C%20and%
20so%20forth.

45

What’s more
ACTIVITY: Phylogenetic Tree

1. Illustrate the Phylogenic Tree of Human Ancestors.


What’s I’ve learned
POST QUIZ: Amino Acid Sequences of in Cytochrome-c
Animals Amino acid Sequence

Horse

Chicken

Frog

Human

Shark

46
Relationships: Tree of
Lesson 9 Life and
Systematics Based on Systematics
Evolutionary

What I need to know


Learning Competency
The learners should be able to Explain how the structural and developmental characteristics and
relatedness in DNA sequences are used to classify living things (STEM_BIO11/12IIIh-j-14)

Specific Learning Outcomes


At the end of the lesson, the learners will be able to:
• describe the multiple lines of evidence used to infer evolutionary
relatedness;
• discuss how anatomical, developmental and relatedness in DNA sequences
are used as evidence to infer the relatedness of taxa; and
• explain that classification is based on evolutionary relatedness

What I know
PRIOR KNOWLEDGE: Define the following terms:

1. Homology 6. Archaea
2. Molecular clock
3. Phylogeny
4. Systematics
5. Tetrapods

What’s new
PRE-ACTIVITY: Answer the following questions.

1. What makes you unique and what makes you similar? To your siblings, mother or father.
Similarities Unique

1.
2.
3.
4.

47
5.

What’s is it
INTRODUCTION:

Lines of evidence to infer evolutionary relationships:


1. Fossil evidence
2. Homologies - Similar characters due to relatedness are known as homologies. Homologies can be
revealed by comparing the anatomies of different living things, looking at cellular similarities and
differences, studying embryological development, and studying vestigial structures within individual
organisms.
Each leaf has a very different shape and function, yet all are homologous structures, derived
from a common ancestral form. The pitcher plant and Venus' flytrap use leaves to trap and digest
insects. The bright red leaves of the poinsettia look like flower petals. The cactus leaves are modified
into small spines which reduce water loss and can protect the cactus from herbivory.

Another example of homology is the forelimb of tetrapods (vertebrates with legs). - Frogs,
birds, rabbits and lizards all have different forelimbs, reflecting their different lifestyles. But those
different forelimbs all share the same set of bones - the humerus, the radius, and the ulna. These are
the same bones seen in fossils of the extinct transitional animal, Eusthenopteron, which
demonstrates their common ancestry.

Organisms that are closely related to one another share many anatomical similarities.
Sometimes the similarities are conspicuous, as between crocodiles and alligators, but in other cases
considerable study is needed for a full appreciation of relationships.

Developmental biology- Studying the embryological development of living things provides clues to
the evolution of present-day organisms. During some stages of development, organisms exhibit
ancestral features in whole or incomplete form.
3. Biogeography- the geographic distribution of species in time and space as influenced by many
factors, including Continental Drift and log distance dispersal.

4. Molecular clocks help track evolutionary time- The base sequences of some regions of DNA change
at a rate consistent enough to allow dating of episodes in past evolution. Other genes change in a less
predictable way.

Classification is linked to Phylogeny

5. Biologists use phylogenetic trees for many purposes, including:


I. Testing hypotheses about evolution
II. Learning about the characteristics of extinct species and ancestral lineages III.
Classifying organisms
The connection between classification and phylogeny is that hierarchical classification is reflected in
the progressively finer branching of phylogenetic trees. The branching patterns in some cases match
the hierarchical classification of groups nested within more inclusive groups. In other situations,

48
however, certain similarities among organisms may lead taxonomists to place a species within a
group of organisms (for example genus or family) other than the group to which it is closely related.
If systematists conclude that such mistake has occurred, the organism may be reclassified (that is
placed in a different genus or family) to accurately reflect its evolutionary history.
49

What’s
moreACTIVITY: Essay
Why do biologists care about phylogenies?
50
Evolutionary
Lesson 10 Relationships:
Systematics Based Taxonomy
on
What I need to know
Learning Competency
The learners should be able to identify the unique/distinctive characteristics of a specific taxon
relative to other taxa STEM_BIO11/12IIIh-j-15

Specific Learning Outcomes


At the end of the lesson, the learners will be able to:
• describe the Linnaean system of classification;
• classify organisms into a hierarchy; and
• construct and use dichotomous keys for identification.

What I know
PRIOR KNOWLEDGE: Definition of Terms

1. Classification 6. Taxonomy 11. Dichotomous key


2. Hierarchy 7. Domain
3. Nomenclature 8. Eukarya
4. Identification 9. Species
5. Description 10. Linnaean Taxonomy

What’s new
PRE-ACTIVITY:

1. Find 10 possible types of writing materials found in your house.


2. Write down the key features to be used in groupings. Place the features in a table
SAMPLE TABLE
Features Ballpen Highlighter Notebook Pencil

Less than 6 - - + -
inches

51
More than 6 + + - +
inches

With Ink + + - -
What’s is it
INTRODUCTION:

The taxonomic system was devised by Carolus Linnaeus (1707-1778). It is a hierarchical system since
organisms are grouped into ever more inclusive categories from species up to kingdom. In 1981, a
category higher than a kingdom, called domain, was proposed by Carl Woese. The table below
illustrates how four species are classified using the present classification system. (Note that it is
standard practice to italicize the genus and species names).
DOMAIN EUKARYA FEATURES
KINGDOM Animalia Organisms that are able to move on their own PHYLUM Chordata
Animals with a backbone
CLASS Mammalia Chordates with fur or hair and milk glands ORDER Primates
Mammals with grasping fingers
FAMILY Hominidae Primates with relatively flat faces and three-dimensional vision
GENUS Homo Hominids with upright position and large brain specific epithet sapiens Members if the
genus Homo with a high forehead and notably thin skull bones
SPECIES Homo sapiens
COMMON NAME human
DOMAIN EUKARYA

KINGDOM ANIMALIA PLANTAE

PHYLUM CHORDATA ARTHROPODA MAGNOLIOPHYTA

CLASS MAMMALIA INSECTA LILOPSIDA

ORDER PRIMATES CANIVORA DIPTERA LILIALES

FAMILY HOMINIDAE CANIDAE DROSOPHILIDA LILIACEAE


E

GENUS HOMO CANIS DROSOPHILIA ALLIUM

Specific Epithet SAPIENS FAMILIARIS MELANOGASTER CEPA

SPECIES HOMO SAPIENS CANIS DROSOPHILIA ALLIUM CAPA


FAMILIARIS MELANOGASTER

COMMON NAME HUMA DOG FRUIT FLY ONION

52

What’s
moreACTIVITY:
1. List down the practical uses of biological classification.
53
Evolutionary
Lesson 11 Relationships: Cladistics
Systematics Based on and Phylogeny
What I need to know
Learning Competency
The learners should be able to describe species diversity and cladistics, including types of evidence
and procedures that can be used to establish evolutionary relationships STEM_BIO11/12IIIh-j-16

Specific Learning Outcomes


At the end of the lesson, the learners will be able to:
• demonstrate how shared derived characters can be used to reveal degrees
of relationship; and
• build cladograms to infer evolutionary relatedness

What I know
PRIOR KNOWLEDGE: Definition of Terms

1. Cladistics 6. Homologous Characters 11. Asteroid


2. Phylogeny 7. Analogous Characters 12. Crinoid
3. Cladograms 8. Clade 13. Holothuroid
4. Character 9. Phylogenic Trees 14. Ophiuroid
5. Character State 10. Echinoid

What’s new
PRE-ACTIVITY:

1. Do you remember the last time you had a family reunion? A summer vacation or a family barbecue
and the latest family picture taken together? Can you describe your family members? What makes
you similar to them and what makes you unique?”
2. list characters or features that served as evidences (e.g. morphological, genetic, etc.) that indeed
they belong to the same family. Note as many as they can think of.
Example:
Family Color Hair Blood Height Shape Shape Skin
Members of the texture/Color Type of the of the Color
Eyes Nose face

54
Father Brown Black Straight B+ 5’7 flat Round Brown
What’s is it
INTRODUCTION:

Basically, a family picture represents a family tree. Family trees show how people are related
to each other. Similarly, scientists use phylogenetic trees like cladograms to study the relationships
among organisms. Sometimes, family trees are used to show relationships between individuals. Those
who are closely related are located closer together than those who are only distantly related. For
instance, in a family tree, we can see that the siblings are close together, indicating a close genetic
relationship. But the siblings are far from their great aunt, indicating a more distant genetic
relationship. Family trees can also be used to see ancestral connections. That is, we can see that all
the people in the last generation have the same great-great-grandparents in common.

What’s more
ACTIVITY: Phylogenic Tree

1. Choose any vertebrates and Create phylogenetic tree showing their evolutionary relationships. This
tree should be primarily based on physical characteristics, such as:
I. Presence or absence of a backbone
II. Ability to breathe in air or water
III. Cold or warm blooded
IV. Carnivore, herbivore, or omnivore
V. Presence or absence of hair/fur
VI. Any other external structures such as horns
2. Research on the internet on the sample of Phylogenic Tree.

What’s I can do
PERFORMANCE TASK:

1. Go online. Choose a group of organisms you are interested to work with (e.g. invertebrates);
2. Download pictures of different species.
3. Print the pictures. In tabular form, list all the characters. Evaluate the characters (whether primitive
or derived).
4. Remember that in building your cladogram, use only shared derived characters.
5. Construct your own cladogram.

55
References
Manuals/Modules/Lesson Exemplar

The Commission on Higher Education. Teaching Guide for Senior High School
General Biology 2

Department of Education Central Office. Most Essential Learning Competencies


( MELCs). 2020.

Websites

1.https://www.britannica.com/science/genetic-engineering
2.https://www.sciencedaily.com/terms/plant_breeding.htm#:~:text=Classical%20plant%20breeding%
20uses%20deliberate,into%20a%20new%20genetic%20background.
3.https://www.genome.gov/genetics-glossary/Genetic
Engineering#:~:text=Genetic%20engineering%20is%20the%20process,selecting%20offspring%20wit
h%20desired%20traits4. https://www.theguardian.com/science/2019/jan/13/the-five-genetically
modified-fruit-edited-bananas-tomatoes
5.https://clarkscience8.weebly.com/geologic-time-scale.html
6.https://www.dogalize.com/2016/12/dog-breeds/
7.https://blogs.scientificamerican.com/observations/the-concept-of-race-is-a-lie/
https://www.encyclopedia.com/science-and-technology/biology-and-genetics/genetics-and
genetic-engineering/hardy-weinberg
law#:~:text=Hardy%E2%80%93Weinberg%20law%20The%20law,generation%2C%20with
%20no%20overlap%20between

8.https://www.ck12.org/book/ck-12-life-science-concepts-for-middle-school/section/4.9/
9.https://www.nature.com/scitable/definition/hardy-weinberg-equation
299/#:~:text=Science%20at%20Scitable-
,Hardy%2DWeinberg%20equation,In%201908%2C%20G.%20H.&text=If%20the%20p%20and%20
q,using%20the%20Hardy%2DWeinberg%20equation.
10.https://www.khanacademy.org/science/biology/her/heredity-and-genetics/a/hardy-weinberg
mechanisms-of-evolution
11.https://www.britannica.com/science/species-taxon

12.https://www.ck12.org/book/cbse_biology_book_class_xi/section/1.3/

13.https://courses.lumenlearning.com/suny-wmopen-biology2/chapter/phylogenies-and-the-history
of
life/#:~:text=In%20scientific%20terms%2C%20the%20evolutionary,closely%20related%2C%20and
%20so%20forth
56

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