Learning Module: Force, Motion and Energy
Learning Module: Force, Motion and Energy
Learning Module: Force, Motion and Energy
LEARNING MODULE
Science G10| Q2
Force, Motion
and Energy
NOTICE TO THE SCHOOLS
This learning module (LM) was developed by the Private Education Assistance
Committee under the GASTPE Program of the Department of Education. The learning
modules were written by the PEAC Junior High School (JHS) Trainers and were used as
exemplars either as a sample for presentation or for workshop purposes in the JHS In-
Service Training (INSET) program for teachers in private schools.
The LM is designed for online learning and can also be used for blended learning and
remote learning modalities. The year indicated on the cover of this LM refers to the year
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revised. For instance, 2017 means the LM was written in SY 2016-2017 and was used in
the 2017 Summer JHS INSET. The quarter indicated on the cover refers to the quarter of
the current curriculum guide at the time the LM was written. The most recently revised
LMs were in 2018 and 2019.
The LM is also designed such that it encourages independent and self-regulated learning
among the students and develops their 21st century skills. It is written in such a way that
the teacher is communicating directly to the learner. Participants in the JHS INSET are
trained how to unpack the standards and competencies from the K-12 curriculum guides
to identify desired results and design standards-based assessment and instruction.
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SCIENCE 10
http://www.bbc.com/news/health-18041884
Nicknamed Photo 51, the image above is the first X-ray diffraction image of the
DNA, deoxyribonucleic acid, which is dubbed as the molecule of life. The
discovery of the DNA structure is one of the most celebrated discoveries of the
20th century, and this photo which provided key information to that discovery has
at least a claim to be the “most important image ever taken.”
In the previous modules, you have explored the concept of inheritance in the
cellular and subcellular level. It is now time for you to look at heredity at the
molecular level, right where it all starts. Among the molecules you will encounter
are DNA and proteins.
What is DNA and why is it so important to heredity? Why are proteins associated
with DNA and traits? How are these proteins synthesized in the cell? How do
LESSON COVERAGE:
In this lesson, you will examine those questions when you take the following
topics:
MODULE MAP:
Here is a simple map of the above lessons you will cover:
(A) 1. During cell division, each new daughter cell must have the same copy
of genetic information found in the DNA. Which of the following refers to
the process of copying a DNA molecule?
A. Replication
B. Transcription
C. Translation
D. Reverse Transcription
(A) 2. In order to produce a protein, segments of the DNA called genes must
be expressed. During transcription, specific segments of the DNA are
copied in order to produce what molecule?
A. Amino acid
B. cDNA
C. Polypeptide
D. RNA
(A) 4. If a mutation has occurred in a gene coding for a specific protein, which
of the following is not likely to occur?
A. Protein will not be formed.
B. Protein will be formed but in lower amounts.
C. Protein will have an additional function.
D. Protein will not have any amino acid.
A. I only
B. I and II
C. I, II, and III
D. I, II, III, and IV
(M) 10. A 38-year old male appears slightly overweight for his 6-foot, pear-
shaped stature. He has narrow shoulders, enlarged breasts, and barely
any facial hair. Recently, he got to see a documentary on genetic
(M) 12. Below is a diagram comparing a normal red blood cell from a sickled
red blood cell. The latter is found in individuals suffering from sickle-cell
anemia.
(M) 13. Which of the following situations illustrate a mutation that may be
passed on by the parent to its offspring?
A. A man with normal chromosomes had a hip X-ray without a
protective shield. A year later, his wife gives birth to a child with a
chromosomal aberration.
B. An embryo missing one copy of chromosome 3 is miscarried very
early in pregnancy.
C. Exposure to excessive UV radiation causes changes in the DNA
of a skin cell, leading to basal cell carcinoma (skin cancer).
D. In a very early human embryo, a mistake in mitosis causes loss of
a chromosome in one daughter cell. The resulting child is a fertile
male.
(M) 14. In 1996, Susan Rosenberg, then a young professor at the University of
Alberta, undertook a risky and laborious experiment. Her
team painstakingly screened hundreds of thousands of bacterial
colonies grown under different conditions. Rosenberg’s findings
suggested that bacteria were capable of increasing their mutation rates,
which might in turn produce strains capable of surviving new conditions.
This raised questions from the scientific community because it
disagrees with which long accepted idea in Biology?
A. Adaptive mutation occurs when microorganisms are able to
choose which genes to mutate.
B. Mutations are much less random and more purposeful.
C. Mutations occur randomly, creating a mixture of harmful,
harmless or beneficial outcomes, which in turn fueled the process
of natural selection.*
D. Organisms can in some cases control how they mutate, enabling
them to more rapidly evolve to adapt to new environments.
(T) 16. Gene duplication is defined as any duplication of a region of DNA that
contains a gene.
You are one of the biologists who believe in the gene-duplication
hypothesis of evolution. If you are asked to explain how gene
duplication can contribute to evolution, which of the following
statements will you most likely use?
A. Mutation can cause the duplication of a gene that allows one
copy of the gene to mutate and evolve to perform a new function.
B. Mutation can cause the duplication of a gene that doubles the
amount and functionality of the trait-causing protein.
C. Mutation can cause the duplication of a gene that may lead to the
production of a disease-causing protein.
D. Mutation can cause the duplication of the whole genome that give
rise to entirely new species.
(T) 17. One of your projects in the Institute of Molecular Biology and
Biotechnology is the creation and distribution of online educational
materials for use by high school students. If you want to explain how
genetic variation is achieved at the molecular level, which of the
following will you use?
A. Brochure
B. Interactive animation
C. Journal Article
D. Lecture
(T) 18. Cuticular proteins are crucial components of the insect cuticle. Qiao et
al (2014) studied a deletion mutation in a gene coding for a cuticular
protein in silkworm, BmorCPR2. The dysfunctional protein lost chitin-
binding ability, leading to reduced chitin content in larval cuticle and
(T) 19. Male house finches (Carpodus mexicanus) vary in the amount of red
pigmentation in their head and throat feathers. Colors range from pale
yellow to bright red. The colors come from carotenoid pigments that are
obtained from the birds’ diet, because no vertebrates are known to
synthesize carotenoid pigments. Thus, it can be said that the brighter
red the male’s feathers are, the more successful he has been at
acquiring the red carotenoid pigment by his food-gathering efforts.
(T) 20. Swine may be infected by a bird flu virus or a human flu virus, or both
viruses in an individual pig at the same time. When both viruses are
present in an individual, it is possible for genes from bird flu virus and
human flu virus to be combined, thereby producing a genetically
distinctive virus, which can then cause widespread disease.
What role could the tiny molecules possibly play in variation? Your goal in this
section is to start exploring this relationship.
Why do people from different parts of the world have different colored skin? Why
do people from the tropics generally have darker skin color than those who live in
colder climates? Variations in human skin color are adaptive traits that correlate
closely with geography and the sun’s ultraviolet (UV) radiation.
As early humans moved into hot, open environments in search of food and water,
one big challenge was keeping cool. The adaptation that was favored involved an
increase in the number of sweat glands on the skin while at the same time reducing
the amount of body hair. With less hair, perspiration could evaporate more easily
and cool the body more efficiently. But this less-hairy skin was a problem because
it was exposed to a very strong sun, especially in lands near the equator. Since
strong sun exposure damages the body, the solution was to evolve skin that was
permanently dark so as to protect against the sun’s more damaging rays.
Melanin, the skin's brown pigment, is a natural sunscreen that protects tropical
peoples from the many harmful effects of ultraviolet (UV) rays. UV rays can, for
example, strip away folic acid, a nutrient essential to the development of healthy
fetuses. Yet when a certain amount of UV rays penetrates the skin, it helps the
human body use vitamin D to absorb the calcium necessary for strong bones. This
delicate balancing act explains why the peoples that migrated to colder geographic
There is also a third factor which affects skin color: coastal peoples who eat diets
rich in seafood enjoy this alternate source of vitamin D. That means that some
Arctic peoples, such as native peoples of Alaska and Canada, can afford to remain
dark-skinned even in low UV areas. In the summer they get high levels of UV rays
reflected from the surface of snow and ice, and their dark skin protects them from
this reflected light.
Process Questions:
1. Describe how skin color differs for the human species.
2. Why do our skin colors vary? Enumerate some of the factors mentioned in the
text.
3. How do you think does variation arise in human skin color? Write your
hypothesis and explain briefly why you came up with such hypothesis.
This is only the first step in your exploration of human skin color variation and the
factors affecting it. You will go back to this case in the succeeding sections of this
module.
In the previous activity, you examined the factors that affect skin color.
Environment plays a big role in the evolution of skin color in humans. A natural
substance, called melanin, gives our skin its color. It also gives color to our hair
and the iris of our eyes.
The traits or characteristics that organisms inherit and possess are provided by
substances found in their bodies. Usually, these trait-giving substances are in
the form of proteins.
Recall what you know about proteins and other biological macromolecules. How
are these proteins synthesized in the cell? Could the differences in the
proteins affect the way organisms grow and develop? To what extent do proteins
influence variety among species? How exactly does variation arise?
Write what you know about these questions in the K column of the K-W-L chart.
Then, write what you want to know about the topic in the W column. Leave the
third column blank.
Each organism has a set of unique and different traits. Learn in this module how
this variation in traits is achieved. Learn further how this variation of traits affects
an organism’s adaptability and survivability. Your task at the end of this unit
will have you explain in the molecular level how traits develop and how
traits vary from generation to generation.
End of EXPLORE:
You looked at variation, which is a broad concept in biology. You looked at
molecules, substances, and proteins which are small entities that play important
roles in organisms.
The contrast of “big” and “small” may have overwhelmed you. But you need not
worry. This module will take you to a guided, step-by-step journey through the
tiny molecules and their huge impact to variation of species and populations.
Gregor Mendel explained in the year 1865 that traits are passed from the parent
to the offspring through “hereditary factors.”
In the early 20th century, scientists establish that Mendel’s “hereditary factors” are
called genes. The gene is the unit of inheritance and different forms of the same
gene are called alleles.
But the individual genes make up a bigger whole. Humans, for instance, have
about 30,000 genes. All these genes are found in a very long genetic material,
the DNA or deoxyribonucleic acid.
http://www.nature.com/scitable/topicpage/dna-is-a-structure-that-encodes-
biological-6493050 - DNA is a structure that encodes biological information
Process Questions:
1. Instructions providing all of the information needed for an organism to grow
and live are found in the DNA. What do these instructions look like? Answer
this question by drawing the detailed structure of DNA in the box provided
below:
2. How can the DNA molecule hold information? Answer this question by
labelling the parts of the DNA structure that enables it to encode a detailed
set of plan for the cells of our body.
3. Why is the DNA considered as the genetic material?
Take note of the important conclusions made by each of the scientists/ group of
scientists who studied DNA. Use the table below to summarize all information:
Process Questions:
1. What are the important conclusions that led the scientists to decide that the
DNA is the substance/molecule of inheritance? Explain.
2. What parts of the DNA structure enables it to perform its function as the
genetic material?
Before you end this activity, complete the exercise found in the link below:
http://www.nobelprize.org/educational/medicine/dna_double_helix/dnahelix.html -
DNA, the Double Helix
Process Questions:
1. What are the components of the DNA molecule?
2. How are these components arranged in order to build a DNA molecule?
3. How is DNA related to proteins? How are proteins synthesized in the cell?
In the previous activity, you studied the DNA molecule. You have already
understood its double-helical structure. You have also seen how its structure
relates to its function as genetic material. Learn more about how “structure fits
In this module, you will come across a lot of reading materials, some of which
may be too long and complicated. For you to better understand the content of the
given materials, always follow these four strategies: (taken from
www.interventioncentral.org)
1. Prediction. Before you begin to read, look at the main title, scan the material
to read the major headings, and look at the illustrations. Based on these
clues, try to predict what the material is about. Write your prediction in the
space provided.
2. List Main Ideas. Stop after each paragraph or major section of the learning
material. Construct one or two complete sentences that sum up only the most
important idea(s) that appear in the section. Good summary sentences
include key concepts or events but leave out less important details. Write
these summary (main idea) sentences down and continue reading.
3. Question Generation. Look at the ideas that you have summarized as you
work through the learning material. For each main idea listed, write down at
least one question that the main idea will answer.
4. Clarifying. Sometimes in your reading you will run into words, phrases, or
whole sentences that really don’t make sense. Here are some ways that you
can clarify the meaning of your reading before moving on:
If you come across a word whose meaning you do not know, read the
sentences before and after it to see if they give you clues. If the word is
still unclear, look it up in a dictionary.
Reread the phrase or sentence carefully and try to understand it. If it
contains words such as “them”, “it” or “they”, be sure that you know what
nouns to which these words refer.
DNA Replication
Predicting Listing Main Questioning Clarifying
Ideas
Summarizing:
Here’s a summary of what I learned about DNA Replication:
Process Questions:
1. Why does the DNA molecule need to make identical copies of itself?
2. Why does DNA replication need to be error-free? Why does the DNA need to
be a “careful reader?”
3. What is the importance of DNA replication to DNA’s function of storing genetic
information?
Quick Review:
Click on the letter that corresponds to the best answer:
1. During DNA replication, the parental strand is GAATCT. What will be the
complementary DNA strand?
A. GAATCT
B. CTTAGA
C. TCTAAG
2. After replication, two identical daughter molecules are produced. Each
daughter molecule contains one old strand of DNA. This is because DNA
replication
A. conservative.
B. continuous.
C. semiconservative.
For nos. 3-5, choose from the following enzymes used in replication.
A. DNA helicase
B. DNA ligase
C. DNA polymerase
3. Unwinds and unzips DNA
You’ve seen from the previous activities how DNA is a very important molecule.
So important that every cell in an organism’s body has to have the same DNA;
and that if ever a cell is to divide itself, it has to first make sure it has identical
copies of its DNA. It is important, during replication, to preserve and pass on the
same information found in the DNA.
The DNA is found inside the nucleus; the molecule does not go out of there.
However, the instructions contained in the DNA go beyond the nucleus to reach
other parts of the cell. How is that made possible by the cell? To answer that
question, you have to get to know another molecule: RNA or ribonucleic acid.
How do genes (which are found in the DNA) give rise to actual traits or
characteristics? If I got that part of my mother’s DNA that tell me I should also
have a curly hair, how come I actually get a curly hair? How do our cells
accomplish that gene expression?
You have now come to the first step in gene expression which is transcription.
The RNA molecule takes part in this process.
http://www.dnalc.org/resources/3d/12-transcription-basic.html - Transcription
http://www.stolaf.edu/people/giannini/flashanimat/molgenetics/transcription.swf -
transcription animation
Process questions:
1. What is transcription?
2. What molecule is produced after transcription? Why does it need to be
produced?
3. What does transcription have to do with protein synthesis?
http://healthland.time.com/2012/09/06/junk-dna-not-so-useless-after-all/ -
Junk DNA – Not So Useless After All
Quick Review:
Click on the letter that corresponds to the best answer:
1. If the sequence of bases in DNA is GACT, then the sequence of bases in
RNA is:
A. GACT
B. GACU
C. CTGA
D. CUGA
2. The process of transcription produces
A. cDNA
B. mRNA
C. protein
3. Which of the following is not true about transcription?
A. In making RNA, uracil, instead of thymine, pairs with adenine.
B. RNA is made from a DNA template.
C. RNA is produced in the cytoplasm of eukaryotic cells.
D. The enzyme RNA polymerase synthesizes RNA.
The first step in gene expression was covered in the previous activity.
“Instructions” from the DNA is transcribed to RNA. RNA is an intermediate
product that serves as a messenger from the nucleus, where the DNA is, to the
ribosomes where proteins will be synthesized. Once the information from the
DNA has been transcribed and the messenger RNA (mRNA) produced, the
mRNA goes out of the nucleus to bring the information to the ribosomes.
Learn more about proteins and their importance through this animation:
http://learn.genetics.utah.edu/content/molecules/proteins/ - What is a Protein?
Proteins are said to be the building blocks of our body. They constitute about
80% of the dry weight of muscle, 70% of the dry weight of skin and 90% of the
dry weight of blood. Proteins make up your hair, skin, eyes, muscle, and organs.
Collagen, for instance, is the protein found in our bones, tendons, and ligaments,
while keratin is the protein of nails, hair, and feathers.
Proteins are also responsible for almost all biochemical processes that keep you
alive.
To produce proteins, information from the DNA (brought by the mRNA) is used.
However, DNA and RNA are both made up of nucleotides, while proteins are
made up of amino acids. They don’t “speak” the same “language.” Hence,
another process must happen for genes to be expressed into protein. This
process is referred to as translation.
Before you go through the process of translation, discover first how the cell
“reads” genes. Read the following excerpt:
Like words in a sentence, the DNA sequence of a gene determines the amino
acid sequence for the protein it encodes. In the protein-coding region of a gene,
the DNA sequence is interpreted in groups of three nucleotide bases, called
codons. Each codon specifies a single amino acid in a protein.
Thesunwashotbuttheoldmandidnotgethishat.
The sun was hot but the old man did not get his hat.
To know what amino acid is coded by a given codon, a genetic code chart is
used:
Notice that the genetic code is degenerate, this means more than one codon
codes for the same amino acid. The genetic code is unambiguous, each triplet
code has only one meaning. Notice also that the code has start and stop signals.
http://www.nobelprize.org/educational/medicine/dna/b/translation/translation.html
- Translation
Process Questions:
1. What information is “translated” in the process of protein synthesis?
2. How does the cell pick up this information? Discuss all the molecules involved
and the action of these molecules.
3. How are proteins synthesized in the cell? Answer this question through a
graphic organizer:
4. Do all cells of the body produce the same protein? Do all genes get
expressed at the same time? Explain.
5. What would happen if a change/irregularity happens in any of the steps? How
will this change affect the protein?
Quick review:
Determine the amino acid coded by the following mRNA codons:
1. CUU
2. ACA
3. GAC
4. UUU
Determine the amino acid sequence that can be produced from this DNA strand:
Recall the first activity you did in this module. It was an analysis of the case of
skin color variation in humans. Retrieve the text as well as your initial analysis to
the case.
Now that you have learned a great deal about DNA and protein synthesis, we
can already discuss the case in more detail. Answer the following questions after
reviewing the text Modern Human Diversity – Skin Color.
1. What are the three factors that affect skin color in humans? Write each factor
in the columns of the given table:
2. How does each of these factors determine whether people will develop lighter
or darker skin color?
To answer this, go back to the text and summarize the main points for each
factor. List the most important ideas and write a summary using as many of the
main idea words as possible. Your list and summary should appear in the
appropriate columns of the table:
How do you think does this substance give color to our skin? Why does it give
a lighter color to one, and a darker color to another? Make a detailed guess
and illustrate that in the box provided below:
At present, the genetics of skin color is still largely unclear, even for the biologists
and experts. In the succeeding section, however, we will still look at some
studies that attempt to know and target the actual genes that control human skin
color and how it varies for peoples of different races.
It doesn’t yet fully answer our query about skin color variation. But, studying
those will deepen your understanding of the molecular basis of inheritance and
genetic variation.
Before ending this section, review and look back at how DNA has come to be
called the substance of inheritance, our genetic material. Show, through a cluster
map, the many substances and processes that rely on the DNA. Use
http://www.spicynodes.org/ to construct your map.
Self-Assessment
Skills
YES A LITTLE NOT YET
I can infer, based on its structure,
that the DNA is the genetic material.
Go back to the previous section and compare your initial ideas with the
discussion. How much of your initial ideas are found in the discussion? Which
ideas are different and need revision?
Now that you know the important ideas about this topic, let’s go deeper by
moving on to the next section.
In the previous section, you learned about the flow of genetic information from
the DNA to the RNA to proteins. That is the central dogma of molecular
biology.
Your goal in this section is to take a closer look at these processes by studying
actual proteins and their synthesis. You will also learn about the consequences
(or benefits) if an error or change occurred in the processing of DNA. Learn how
such changes may have implications to an organism’s adaptation and survival.
The process of replication is not entirely error-free. Changes may happen to the
DNA sequence. Such change is called mutation.
What happens if there is a mutation in the DNA sequence? Click on the link
below to do an activity about mutation. In this virtual lab, you will complete mRNA
and protein sequences based on the given information. Compare the original and
mutated sequences to see the impact of the mutation.
Process Questions:
1. Describe the differences between the original and mutated sequences.
Learn more about mutation by exploring the learning materials found in the
following links:
http://www.uvm.edu/~cgep/Education/Mutations.html - Mutations
In order for you to get the most out of the materials provided, you will be
introduced to another writing strategy.
Just as the cell transcribes and translates information from the DNA, you will also
try to “transcribe” and “translate” the information given about mutation using the
POW+TREE Strategy.
Reason
Explanation
Ending
Many known diseases are caused by mutation. Click on the link below to learn
about some common genetic disorders:
http://www.steadyhealth.com/articles/The_16_Most_Common_Genetic_Diseases
_a1547.html - The 16 Most Common Genetic Diseases
4. As you have read, these diseases are usually resulting from lack of a
necessary protein or presence of wrong or malfunctioning proteins. How
does mutation contribute to the production of faulty proteins?
Quick Review:
Review the animation and answer the questions that follow to test your
understanding.
http://highered.mheducation.com/sites/0072552980/student_view0/chapter9/ani
mation_quiz_5.html - Addition and Deletion Mutations
You have looked at mutation and the effects it may have in protein synthesis.
You have also explored real situations related to the said topic.
This next activity will have you examine more real-life situations that illustrate
protein synthesis.
PROBLEM 1
Process Questions:
1. Why is it possible for a firefly to produce its own light?
2. How is the protein (luciferase) synthesized in the cell? What results from
this?
3. If the synthesis is altered, what is the possible outcome?
PROBLEM 2
Viruses are obligate intracellular parasites, and their replication requires host cell
functions. Although the size, composition, complexity, and functions encoded by
their genomes are remarkably diverse, all viruses rely absolutely on the protein
synthesis machinery of their host cells. Lacking their own translational apparatus,
they must recruit cellular ribosomes in order to translate viral mRNAs and produce
the protein products required for their replication. In addition, there are other
constraints on viral protein production. Crucially, host innate defenses and stress
responses capable of inactivating the translation machinery must be effectively
neutralized. Furthermore, the limited coding capacity of the viral genome needs to
be used optimally. These demands have resulted in complex interactions between
virus and host that exploit ostensibly virus-specific mechanisms and, at the same
time, illuminate the functioning of the cellular protein synthesis apparatus.
Process Questions:
1. What determines the size, composition, complexity, and functions of a virus?
2. How are viral proteins synthesized if viruses don’t have cells?
3. What may happen if the viral protein synthesis is altered? Why do many
scientists find ways to alter this process in viruses?
PROBLEM 3
You have looked at different situations related to protein synthesis. Put together
in the table below your answers to the essential question that was asked for each
problem.
Process Questions:
1. Look at your answers to the essential question in the above table. What do all
the answers have in common?
2. Are all the factors the same? How do the answers differ? What are the
different factors that affect protein synthesis in cells?
3. Complete the following statement and support your answer with examples
from the above situations.
Be sure that everything is clear to you before you move on to the next activity.
Use the following self-monitoring guide:
It is now time for you to go back to the case you have been investigating in the
previous sections.
Melanin is the substance that gives skin, hair, and eyes their color. Melanin is
also found in the light-sensitive tissue at the back of the eye (the retina), where it
plays a role in normal vision. Melanin is produced in specialized cells called
melanocytes.
The TYR gene provides instructions for making the enzyme tyrosinase.
Process Questions:
1. How is tyrosinase (a protein) synthesized in the cell? Based on what you
know about gene expression and protein synthesis, make a simple model of
the synthesis of tyrosinase from the TYR gene.
The next activity will help you analyze this case more deeply. The focus is on
genetic variation.
To help you understand how genetic variation occurs at the molecular level,
watch carefully the following videos and answer the questions that follow:
VIDEO 1
Process Questions:
1. According to the video, what makes it possible for new genes to enter a
population?
2. How does genetic variation arise?
VIDEO 2
Process Questions:
1. What are heritable mutations?
2. How can mutations in genes be passed from the parent to offspring?
Before you leave this topic on heritable mutations, spend some time thinking
about this additional question: Does mutation happen randomly or does it
happen as a response to the environment? Gather pertinent resources and
discuss this controversial issue with your classmates through an online
discussion forum.
VIDEO 3
Process Questions:
1. In terms of genetic variation, why is sexual reproduction more advantageous
than asexual reproduction?
2. How does genetic variation arise from sexual reproduction?
You have looked at three different videos related to genetic variation. Put
together in the table below your answers to the essential question that was asked
for each problem.
1. Look at your answers to the essential question in the above table. What do all
the answers have in common?
2. Are all the factors the same? How do the answers differ? What are the
different ways by which genetic variation can be attained?
3. Complete the following statement:
Process questions:
1. Describe the situation of alpine chipmunks (Tamias alpinus) in the Yosemite
National Park. Why is it now difficult for park visitors to encounter the
chipmunks?
2. Discuss all the factors that led to the supposed loss of genetic variation in
alpine chipmunks.
3. Based on the analysis you’ve done, suggest measures that may be taken in
order to improve genetic variation in alpine chipmunks.
Recall the two focus questions that you dealt with in the different activities:
How are proteins synthesized in the cell?
How does genetic variation arise?
Write your final answers to these questions in the L column of the K-W-L chart.
Compare your new answers with your answers in the previous columns.
K-W-L Chart
End of DEEPEN:
In this section, the discussion was about mutation and genetic variation.
What new realizations do you have about the topic? What new connections have
you made for yourself? What helped you make these connections?
Now that you have a deeper understanding of the topic, you are ready to do the
tasks in the next section.
You now reached the concluding part of this case analysis of human skin color
variation. This time, you will write your own analysis of the case based on the
topics you learned about gene expression, mutation, and genetic variation.
http://www.scientificamerican.com/article/researchers-identify-huma/ -
Researchers Identify Human Skin Color Gene
http://medicalxpress.com/news/2014-01-skin-gene-global-populations-reveal.html
- Studies of a skin color gene across global populations reveal shared origins
http://humanorigins.si.edu/evidence/genetics/skin-color/modern-human-diversity-
genetics - Modern Human Diversity – Genetics
Process Questions:
1. Why is there variation in human skin color?
2. Why is this variation important?
You will communicate the information you gathered and your analysis to your
classmates. Choose the mode which you think will best communicate your
thoughts. Use a project planning map to guide you through this task. See
sample map below.
CRITERIA YES NO
I have a clear idea of what the case is about. I
asked questions and defined problems / variables.
One of your projects in the Institute of Molecular Biology and Biotechnology is the
creation and distribution of online educational materials (videos, video podcasts,
interactive simulations, etc.) that explain the molecular basis of genetic variation
and species adaptability.
The responsibility of producing the materials is left to the media team composed
of a researcher, a scriptwriter, and an animator.
Materials are intended for students and are therefore expected to be informative,
engaging, and creative.
Thorough
research was
done and all
sources of
information
are clearly
identified and
credited using
citations.
End of TRANSFER:
In this section, your task was to explain in different ways how genetic variation is
achieved at the molecular level and discuss its implications to biodiversity and
the species’ adaptability and survivability.
How did you find the performance task? How did the task help you see the real
world use of the topic?
You have completed this lesson. Before you go to the next lesson, you have to
answer the following post-assessment.
amino acid Organic molecule having an amino group and an acid group, which
covalently bonds to produce peptide molecules.
DNA replication Synthesis of a new double helix prior to mitosis and meiosis in
eukaryotic cells and during prokaryotic fission in prokaryotic cells
enzyme Organic catalyst, usually a protein, that speeds a reaction in cells due to
its particular shape.
genetic code Universal code that specifies protein synthesis in the cells of all
living things. Each codon consists of three letters standing for the DNA
nucleotides that make up one of the 20 amino acids found in proteins.
messenger RNA (mRNA) Type of RNA formed from a DNA template that bears
coded information for the amino acid sequence of a polypeptide.
ribosome RNA and protein in two subunits; site of protein synthesis in the
cytoplasm.
transfer RNA Type of RNA that transfers a particular amino acid to a ribosome
during protein synthesis.
http://humanorigins.si.edu/evidence/genetics/skin-color/modern-human-diversity-
skin-color - Modern Human Diversity – Skin Color
http://www.nature.com/scitable/topicpage/dna-is-a-structure-that-encodes-
biological-6493050 - DNA is a structure that encodes biological information
http://www.nobelprize.org/educational/medicine/dna_double_helix/dnahelix.html -
DNA, the Double Helix
http://www.dnalc.org/resources/3d/12-transcription-basic.html - Transcription
http://www.stolaf.edu/people/giannini/flashanimat/molgenetics/transcription.swf -
transcription animation
http://healthland.time.com/2012/09/06/junk-dna-not-so-useless-after-all/ - Junk
DNA – Not So Useless After All
http://healthyeating.sfgate.com/6-primary-functions-proteins-5372.html - 6
Primary Functions of Proteins
http://www.nobelprize.org/educational/medicine/dna/b/translation/translation.html
- Translation
http://highered.mheducation.com/olcweb/cgi/pluginpop.cgi?it=swf::535::535::/site
s/dl/free/0072437316/120077/micro06.swf::Protein+Synthesis – Protein
Synthesis
http://www.uvm.edu/~cgep/Education/Mutations.html - Mutations
http://www.steadyhealth.com/articles/The_16_Most_Common_Genetic_Diseases
_a1547.html - The 16 Most Common Genetic Diseases
http://highered.mheducation.com/sites/0072552980/student_view0/chapter9/ani
mation_quiz_5.html - Addition and Deletion Mutations
http://evolution.berkeley.edu/evolibrary/news/120301_chipmunks - Climate
change causes loss of genetic diversity
http://www.scientificamerican.com/article/researchers-identify-huma/ -
Researchers Identify Human Skin Color Gene
http://medicalxpress.com/news/2014-01-skin-gene-global-populations-reveal.html
- Studies of a skin color gene across global populations reveal shared origins
http://humanorigins.si.edu/evidence/genetics/skin-color/modern-human-diversity-
genetics - Modern Human Diversity – Genetics
http://labtestsonline.org/assets/images/article_images/KARO+21.jpg – Down
syndrome karyotype
http://www.nature.com/scitable/content/sickle-shaped-and-normal-red-blood-
cells-21172 - Normal and sickle-shaped red blood cells
http://worms.zoology.wisc.edu/zooweb/Phelps/ZWK99034k.jpeg - Patau
syndrome karyotype
http://healertoday.com/wp-content/uploads/2013/08/ALS-Stephen-Hawking.jpg -
Stephen Hawking
(A) 2. The sequence found in the mRNA molecule determines the following
except:
A. the protein that will be synthesized.
B. the amino acids to be brought by mRNA.
C. the complementary DNA sequence.
D. the amino acids that will form a protein.
(A) 4. A mutation in a DNA segment can possibly lead to the following except
A. change in amino acid sequence.
B. synthesis of a different protein.
C. no change in the protein that will be formed.
D. retention of the original position of the bases in the gene.
(A) 5. Consider this DNA sequence: AGT CGA GGC. If an adenine base (A)
is added to the sequence such that the new sequence copied during
replication is AGT ACG AGG C, what kind of mutation has occurred?
A. Chromosomal aberration
B. Frameshift mutation
C. Point mutation
D. Polyploidy
(A) 8. Refer to the given genetic code chart to predict which mutation that
changed the mRNA codon would be most likely to affect protein
function.
They allowed the phages to infect the bacteria for a short time. Then,
the bacterial cells were pelleted in a centrifuge. They found that the
radioactive DNA was always found with the bacterial cells while the
radioactive protein was always in the supernatant (outside of the
bacterial cells).
During a phage infection, it was determined that some part of the phage
was injected into the bacterium and it was this injected material that
conveyed the genetic material necessary to produce new phages.
Having said this, which of the following is the conclusion made by
Hershey and Chase about the genetic material of bacteriophages?
A. DNA is the genetic material.
(M) 10. Linda Hunt is an American actress known as one of the lead characters
in the TV series NCIS. She has taken a variety of roles both on TV and
in the movies in her more than 3 decades as an actress. Her efforts
have not gone unnoticed as she has received recognition from
numerous award-giving bodies. Linda has Turner syndrome, a condition
wherein a female would have a single X chromosome instead of the
usual pair. What could be a possible consequence of having just a
single X chromosome?
A. taller than usual because of genes that promote bone
development
B. there could be missing genes that lead to undeveloped
reproductive organs
C. inhibited breast development because of inactivated genes in the
Y chromosome
D. increased muscle mass from genes found in the Y chromosome
(M) 12. Amyotrophic lateral sclerosis (ALS), often referred to as “Lou Gehrig’s
Disease,” is a progressive neurodegenerative disease that affects nerve
cells in the brain and the spinal cord. Early symptoms of ALS often
include increasing muscle weakness, especially involving the arms and
legs, speech, swallowing or breathing. When muscles no longer receive
the messages from the motor neurons that they require to function, the
muscles begin to “atrophy” or become smaller.
Most cases of ALS are sporadic, however some are genetic and are
attributed to a faulty gene. For instance, mutation in superoxide
dismutase 1 (SOD1) gene which affects the SOD1 protein is associated
with ALS symptoms.
What is the most likely explanation for this genetic cause of ALS?
A. During replication, a change in the SOD1 gene occurred that led
to the synthesis of SOD1 protein with a new and toxic function.
B. During transcription, a copying error occurred in the mRNA
transcript of SOD1 gene which led to the production of a defective
SOD1 protein.
C. During translation, an incorrect amino acid becomes attached to
the tRNA molecule thereby causing a change in the SOD1 protein
structure.
D. During protein folding, a lack of enzyme causes incorrect folding
and modification of the SOD1 protein structure.
(M) 14. A paper entitled “To Mutate or Not to Mutate” was posted in the Institute
of Science in Society website. A quote from the paper goes:
Contrary to views widely held not so long ago, genes do not as a rule
mutate at random, and cells may choose what, or at least, when to
mutate.
(T) 15. You are one of the invited guests in the annual biologists’ forum. This
year’s topic is “mutation-driven evolution.” You’ve made a number of
studies about the said topic and you’ve decided that your talk will focus
on which of the following?
A. Causes and mechanisms of mutation
B. Darwin’s theory of natural selection
C. Effects of mutation on population
D. Evidences of species’ evolution by mutation
(T) 16. You are a writer for the journal Trends in Evolution. If you are currently
writing an article entitled “Evolution by Gene Duplication,” which of the
following will you not include in your article?
A. In all three domains of life – bacteria, archaebacteria, and
eukaryotes – large proportions of genes were generated by gene
duplication.
B. Many genome sequences are determined and analyzed that
demonstrated the prevalence and importance of gene duplication.
C. Many studies concluded that the origin of a new function appears
to be a very rare fate for a gene that has been duplicated.
D. The doubling of a chromosomal band in a mutant of the fruit fly
Drosophila melanogaster exhibited extreme reduction in eye size.
(T) 18. Cystic fibrosis is an autosomal recessive disorder that causes thick,
sticky mucus to build up in the lungs, digestive tract, and other areas of
the body. It is one of the most common chronic lung diseases in
children and young adults.
Mutations in the CFTR gene cause cystic fibrosis. The CFTR gene
encodes an ion transporter protein normally expressed in the
respiratory and digestive tracts. Individuals homozygous for mutated
CFTR gene died at very early ages then due to lack of advanced
medical intervention. Despite this, the mutation persists at relatively
high frequency in populations of European descent. A possible
explanation is that heterozygotes for such mutations are said to gain
immunity to the lethal effects of diseases such as typhoid fever. Which
of the statements below is most accurate?
A. The cystic fibrosis mutation is a beneficial mutation.
B. The cystic fibrosis mutation is a conditional mutation.
C. The cystic fibrosis mutation is a lethal mutation.
D. The cystic fibrosis mutation is a neutral mutation.
Over the course of time, what should occur in order to maintain genetic
variation?
A. Methylated DNA should become fixed in the genes of all bacterial
species.
B. Non-methylated DNA should become fixed in the genome of all
bacteriophages.
C. Gene for DNA methylation should be eliminated in the
populations over time.
D. Methylated and non-methylated strains should be maintained
among both bacteria and bacteriophages.