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BIOTECHNOLOGY
Guided Learning Activity Kit
Tools used in Genetic Engineering
in Humans
Quarter 3- Week 3
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Biotechnology – Grade 8
Guided Learning Activity Kit
-Tools used in Genetic Engineering in Humans-
Quarter 3- Week 3
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Introduction
In this activity, you will learn on how to describe the tools that are
commonly used in genetic engineering especially to humans and expose
yourself to ethical issues concerning human genetic engineering.
Learning Competency
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Objectives
At the end of this guided learning activity, you are expected to:
Identify the different tools used in genetic engineering in
humans.
Describe the function of the different tools used in human
genetic engineering.
Discuss the ethical issues involve in the used of different tools
of human genetic engineering.
Review
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fetus).
Discussion
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Figure 1. The human insulin gene is inserted into a bacterial plasmid. This recombinant
plasmid can then be used to transform bacteria, which gain the ability to produce the insulin
protein.
In this lesson, we will be tackling about what are the tools used in
order to engineered human genetically.
1. Source of DNA - Target (foreign) DNA – DNA taken from one organism to
be placed into the DNA of a second organism. Since in this case we are
discoursing about human genetic engineering, human DNA is used in
combination with the bacterial plasmid.
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Figure 2. Electron micrograph of a bacterial DNA plasmid (chromosome fragment)
https://en.wikipedia.org/wiki/Plasmid#/media/File:Plasmid_em-en.jpg
Characteristics of Vectors
• Capable of carrying a significant piece of the donor DNA
• Readily accepted by the host
• Must have a promoter in front of the cloned gene
• Vectors (such as plasmids and bacteriophages) should have three
important attributes:
– An origin of replication somewhere on the vector
– Must accept DNA of the desired size
– Contain a gene that confers drug resistance to their cloning host
3. Host cell – the cell into where the new gene is transplanted. Host cells
are bacterial cells which take up the recombinant DNA. Since DNA is
hydrophilic (attracted to water molecules or can be dissolved in water), it
cannot pass through the cell membrane of bacteria easily.
4. Enzymes
◦Restriction Endonucleases – Enzymes that act as scissors which can
cut or fragment strands of DNA crosswise at selected positions
•Found primarily in bacteria
• Each has a known sequence of 4 to 10 pairs as its target
• Can recognize and clip at palindromes, sequence that reads
the same backward as forward
• Can be used to cut DNA into smaller pieces for further study
or to remove and insert sequences.
• Can make a blunt cut or a “sticky end”
• The pieces of DNA produced are called restriction fragments.
• Differences in the cutting pattern of specific restriction
endonucleases give rise to restriction fragments of differing lengths-
restriction fragment length polymorphisms.
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Table 1 Examples of Some Restriction Endonucleases and Their Properties
Restriction Source Target Sites Recognizes Product
Endonuclease (Bacterial (Cuts at (Base Pairs)
s Species) Arrow)
Serratia C-C-C-G-G-G
Sma I 6 Blunt ends
marcescens G-G-G-C-C-C
Haemophilus G-G-C-C
Hae III 4 Blunt ends
aegyptius C-C-G-G
J. Ingraham and C. Ingraham, Introduction to Microbiology. Copyright 1995 Wadsworth Publishing Co.
Restriction Enzymes are named from the organisms from which they
are isolated. For example, EcoRI isolated from E. coli RY13: Eco comes from
the first letter of the genus name and the first two letters of the species
name; R if for the strain type and I is for the first enzyme for that type.
Hence, BamHI is isolated from Bacillus amyloliquefaciens strain, and Sau3A
is isolated from Staphylococcus aureus strain 3A.
◦ Ligases – enzyme that join two DNA segments together which acts
like a glue sticking foreign DNA to DNA of the cloning vector. It will only
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work if DNA from the two DNA sources has been cut with the same
restriction enzyme i.e. sticky ends of cut DNA will be complementary to each
other.
https://blog.addgene.org/plasmids-101-restriction-cloning
Figure 3. Overview of the restriction cloning process. Both the plasmid (blue, backbone) and
the DNA sequence of interest (green, insert) are cut with restriction enzymes to generate
compatible overhangs that allow them to bind.
2. Designer Babies
This ability to “design” a baby, recombinant DNA technology critics
argue, would cause a generation of youngsters whose terribly make-up was
formed by parental whims, economic process, perpetually shifting standards
of beauty and social group preferences. It could lead on to a constantly
deepening divide between those people who were genetically improved and
people who weren't. This divide may follow current category lines betting on
the financial price of recombinant DNA technology. This incorporation of a
genetic element to the “haves” and “have nots” might additionally cause a
brand-new variety of bioscience or maybe the split of humanity into 2
distinct species.
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Proponents of human genetic engineering, however, argue that such
claims have very little basis. Sex relies entirely on the presence or absence
of the Y chromosome whereas traits like hair and eye color are controlled by
many various genes.
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semi-permanent consequences of genetic modification don't seem to be
however understood. Still, the waste of human embryos or given eggs grates
on individuals, particularly people who struggle to conceive. Some people
who believe in fertility treatments or in vitro fertilization see the employment
of embryos in medical analysis as a waste of viable eggs.
7. Lengthened Lifespan
Researcher determined that human genetic engineering has the
potential to lengthen the lifespan of an individual. Experts have identified a
portion of human chromosomes that is responsible for knowing how
frequent a cell can divide and, how long an organism can live.
Opponents of these, argument out that the earth is already stressed
to support the foregoing population which is approximately 7.2 billion so
lengthening the humane average lifespan could contribute to the struggling
planet.
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Scientists typically like modifying already existing or extinct
microorganism and viruses to supply new strains that may defeat our
immunity, vaccines, and drugs. Sometimes, they like making new viruses
and microorganism from scratch. Nevertheless, these strains are not
constantly hazardous to humans even they can be fatal to another
organism.
Activities
Guided Practice 1
Carefully read the statement. Used the word bank to identify the word that
is being described by the statement and phrases below.
Vectors Plasmid DNA
Host Cell Target DNA Restriction
Enzyme
Exonuclease Ligase Recombinant
DNA
Genetic Engineering
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_________________4. A type of vector that is commonly used, circular form of
DNA in bacteria.
_________________5. An organism/ chemical that is used to transport a gene
to the host cell.
_________________6. Enzyme that acts as proofreaders to increase the
consistency of DNA synthesis.
_________________7. They are found in the nucleus that carries genetic
material of certain living organism.
_________________8. DNA taken from one organism to be placed into the DNA
of a second organism.
_________________9. These are special enzymes used to cut the DNA at
specific places.
________________10. The cell into where the new gene is transplanted.
Guided Practice 2
Using the table below as reference, each letter has a corresponding
code, decipher the word to complete the sentences below.
ALPHABET CODE
A B C D E F G H I J K L M
N O P Q R S T U V W X Y Z
2. ___ ___ ___ ___ ___ ___ is an organism/ chemical that is used to transport
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3. Ligase are ___ ___ ___ ___ ___ ___ that join two DNA segments together
in genetic engineering.
6. The pieces of DNA produced by restriction endonucleases are called
restriction ___ ___ ___ ___ ___ ___ ___ ___ ___.
7. Host cell are cells which into where the new ____ ___ ___ ___ is
transplanted.
8. Restriction Enzymes are named from the ___ ___ ____ ____ ____ ___ ___ ___
10. In 1982 ___ ____ ___ ___ ___ ___ ___ became the first GMO
Independent Practice
Find in the pictogram and list the words you found on the blank below. After
you found all eight words, make your own conclusion or generalization using those
words.
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Indicators Points
You made a meaningful idea using all 10
the eight words.
You made a meaningful idea using six 8
to seven words.
You made a meaningful idea using all 6
the four to five words.
You made a meaningful idea using all 4
the two to three words.
You made a meaningful idea using all 2
the one word.
__________________________________________________________________________________
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__________________________________________________________________________________
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__________________________________________________________________________________
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Assessment
_________3. These are the commonly used vectors for human genetic
engineering.
A. Plasmids C. Viral vectors
B. Cosmids D. Artificial chromosomes
_________4. These are enzymes that act as scissors which can cut or
fragment strands of DNA crosswise at selected positions.
A. Ligases C. Exonucleases
B. Restriction endonucleases D. Cellulase
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3. Be able to transfer desired genes from one organism to
another
4. Find new ways to create aliens or superheroes
A.1, 2 B. 1, 2, 3 C. 1, 3 D. 1, 2, 3, 4
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For questions 9-10, used the diagram below to answer.
Reflection
Learning Logs
Fill in the blank with your perceptions about the discussion by
completing the statements below. Write your answer in a separate sheet of
paper.
I learned about
______________________________________________________________________
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The part that is the most confusing is
______________________________________________________________________
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In my belief, is it just to modify the human genome? Why or why not?
______________________________________________________________________
Reference
s
"What Is A Gene? (For Kids) - Nemours Kidshealth". 2020. Kidshealth.Org.
https://kidshealth.org/en/kids/what-is-gene.html.
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"Genetic Engineering". 2020. Slideshare.Net.
https://www.slideshare.net/drpriyankaclre/genetic-engineering-
40237744.
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Key to Corrections
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Review
1. GENE Assessment
2. DEOXYRIBONUCLEIC ACID 1. D
3. ENZYME 2. A
4. NUCLEUS 3. A
5. EMBRYO 4. B
5. B
Guided Practice 1 6. D
1. Genetic Engineering 7. A
2. Ligase 8. A
3. Recombinant DNA 9. C
4.Plasmid 10. A
5. Vectors
6.Exonuclease
7.DNA
8. Target DNA
9.Restriction Enzyme
10. Host Cell
Guided Practice 2
1. Recombinant
2. Vector
3. Enzyme
4. DNA
5. Plasmid
6. Fragments
7. Gene
8. Organism
9. Lifespan
10. Insulin
Independent Learning
Vectors
Enzyme
Genetic Engineering
Plasmids
Host Cell
Tools
DNA
Human
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Acknowledgment
Finally, the parents and other home learning facilitators for giving the
learners the needed guidance and support for them to possibly accomplish the
tasks and for gradually helping them become independent learners.