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SCIENCE 10-DLP11-GenCode-Mutation-Types-Disorders
SCIENCE 10-DLP11-GenCode-Mutation-Types-Disorders
GRADE 10
Learning
DAILY
Teacher: Sharlene Cecil O. Pagobo Area: Science
LESSON PLAN
Teaching Dates & Time: March 2024 Quarter: 3rd
I. OBJECTIVES
The learners demonstrate an understanding of mutations that occur in sex cells as
A. Content Standards
being heritable.
B. Performance Standards
Explain how may cause changes in the structure and function of a protein.
C. Learning Competencies
(S10LT-IIIe-38)
K: Explain the concept of mutation and differentiate the kinds of chromosomal
mutations.
D. Learning Objectives
S: Draw or describe a hypothetical hybrid organism.
A: Infer the possible results should there be any changes in the genetic codes.
Genetic Code Table, Mutation: (Types and Disorders), & Genetic Engineering
II. CONTENT
and Karyotyping
III. LEARNING RESOURCES
A. References
1. Teacher’s Guide pages 208-212
2. Learner’s Materials pages 281-293
3. Textbook pages
4. Additional Materials from
Learning Resource
(LR)portal
B. Other Learning Resources Powerpoint presentation, pictures, animation, video clip
IV. PROCEDURES
ELICIT
A. Reviewing previous lesson or Briefly recall the Genetic Code Table from the previous lesson.
presenting the new lesson
ENGAGE Present figure 8 found in page 281 relating it to student’s experiences when
B. Establishing a purpose for the copying notes in the board.
lesson Let the students analyze the figure.
Mutations can occur in two different types of cells: reproductive cells and body
cells. Only mutations in sex cells pass on to offspring.
There are two types of mutations that can occur in gamete cells:
Gene mutation is a permanent change in the DNA sequence that makes up a
gene.
Types:
o Point mutation. This may lead to substitution mutation.
Nonsense, Missense, and Silent mutation
o Frameshift mutation
Chromosomal mutation occurs at the chromosome level resulting in gene
deletion, duplication or rearrangement that may occur during the cell cycle
and meiosis. It may be caused by parts of chromosomes breaking off or
rejoining incorrectly.
Types:
o Deletion
o Duplication
o Inversion
o Insertion
o Translocation
Most mutations are harmful. Some mutations in a body cell are known to cause
cancer, while mutations in sex cells can cause birth defects. A severe mutation may
lead to cell death and may have no effect on the body. Sometimes mutations may
be useful for the species. For example, a mutation in blood proteins prevents
viruses or parasites to thrive in host organisms.
The gain or loss of chromosome material can lead to a variety of genetic disorders.
Human examples are the following:
1. Cri du chat
2. Down Syndrome (Trisomy 21)
3. Edwards Syndrome (Trisomy 18)
4. Jacobsen Syndrome (Terminal 11q Deletion Disorder)
5. Klinefelter’s syndrome (XXY)
6. Turner’s syndrome (X instead of XX or XY).
Human Karyotyping
Some of the abnormalities associated with chromosome structure and number can
be detected by a test called a karyotype. A karyotype is an image of the full set of
chromosomes of an individual that displays the normal number, size, and shape.
Karyotypes may reveal the gender of a fetus or test for certain defects through
examination of cells from uterine fluid – a procedure called amniocentesis – or
through sampling of placental membranes.
Genetic Engineering
Understanding the gene has led to the remarkable
development of methods for changing a cell’s DNA. A
modern biotechnology called genetic engineering produces
transgenic or GM (genetically modified) crops of organisms.
Scientists have developed methods to move genes from one species into another.
When DNA from two different species is joined together, it is called recombinant
DNA.
B. Matching Type. Match the type of mutation to its definition and disorder.
Mutation Definition
Deletion a. when a part of a chromosome is copied (duplicated) too many times.
Duplication b. When a segment of a chromosome is reversed end to end.
Inversion c. Segments of two chromosomes are exchanged.
Insertion d. When a base is deleted from the nitrogen base sequence.
e. The addition of one or more nucleotide base pairs into a DNA
Translocation
sequence.