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WGU Biochemistry Final Review Latest-1. The polymerase chain reaction is a tool used to study protein structure. True False - False Feedback PCR is a tool used to amplify a specific segment of DNA. What color is the primer in the following diagram? Red Purple Blue - Red Feedback ...

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WGU Biochemistry Final Review Latest
1. The polymerase chain reaction is a tool used to study protein structure.

True
False - False

Feedback
PCR is a tool used to amplify a specific segment of DNA.

What color is the primer in the following diagram?

Red
Purple
Blue - Red

Feedback
Recall from the section on DNA replication that DNA polymerase needs a primer to
begin DNA synthesis. This requirement means the primers will direct the DNA
polymerase to only synthesize complementary strands of the target DNA. (Note: In
DNA replication, the primers are RNA primers, while PCR generally uses DNA
primers because they are more stable.)

dNTPs are DNA nucleotides used in PCR.

True
False - True

Feedback
dNTPs stands for deoxynucleotide triphosphates, which are the nucleotides used in
DNA synthesis.

A thermocycler is a machine used for PCR that varies the temperature of a sample.

True
False - True

Feedback
For PCR, in each cycle, the two strands of the duplex DNA are separated by heating,
then the reaction mixture is cooled to allow the primers to anneal (or pair) to their
complementary segments on the DNA. Next, the DNA polymerase directs the

,synthesis of the complementary strands. The use of a heat-stable DNA polymerase
eliminates the need to add fresh enzyme after each round of heating (heat inactivates
most enzymes). Hence, in the presence of sufficient quantities of primers and dNTPs,
PCR is carried out simply by cycling through the different temperatures for strand
separation, primer annealing, and DNA synthesis.
The thermocycler is the machine that is used to vary the temperature of the samples.

DNA polymerase is used in DNA replication and in PCR.

True
False - True

Feedback
Both PCR and DNA replication require DNA polymerase to make new copies of DNA.

Which of the following changes can NOT be detected using PCR?

Differences in DNA sequence
Epigenetic changes
Deletions
Insertions - Epigenetic changes

Feedback
Epigenetic changes do not affect the sequence of the DNA. PCR is used to look at the
DNA sequence.

Which of the following components is NOT used in PCR?

DNA template
DNA nucleotides
RNA polymerase
Primers - RNA polymerase

Feedback
PCR makes a DNA copy, so DNA polymerase is used.

Assuming there is one copy of the target DNA sequence before PCR, how many copies
of DNA are there after 5 PCR cycles?

256
6
65,536

,16
32 - 32

Feedback
Each cycles double the numbers of DNA copy. Round 1: 1->2. Round 2: 2 ->4. Round
3: 4 -> 8. Round 4: 8 ->16. Round 5: 16 ->32.

DNA polymerase can synthesize new DNA strands in which direction?

3' to 5'
5' to 3'
any direction
N-terminus to C-terminus - 5' to 3'

Feedback
DNA needs a free 3' end to bind to and initiate synthesis of a DNA. It synthesizes in a
5' to 3' direction.

The following are steps involved in a polymerase chain reaction. Which is the correct
order:

Elongation, denaturation, and annealing
Denaturation, annealing, and elongation
Annealing, elongation, and denaturation
Elongation, annealing, and denaturation - Denaturation, annealing, and elongation

Feedback
PCR uses repeated cycles of temperature to amplify particular DNA segments. In the
first step, the reaction mixture is heated to separate the DNA strands (denaturation).
The reaction is then cooled to allow the DNA primers, which define the sequence to be
amplified, to anneal (base pair) with the template DNA. In the third step, DNA
polymerase extends the DNA primers to create a copy of the target DNA sequence.
Heating the reaction to stop polymerization and separate the DNA strands starts the
cycle over again

Sickle Cell Anemia is inherited in an autosomal recessive pattern. Choose the set of
chromosomes of a person that has inherited the disease. Green boxes represent normal
alleles and yellow boxes represent mutant alleles.
Captionless Image

A. Chromosome 12 (Blue) vs. Chromosome 11 (Red)
B. Chromosome X (Blue) vs. Chromosome Y (Red, Short)

, C. Chromosome 11 (Blue) vs. Chromosome 11 (Red w/green stripe)
D. Chromosome 11 (Blue) vs. Chromosome 11 (Red w/yellow stripe) - D.
Chromosome 11 (Blue) vs. Chromosome 11 (Red w/yellow stripe)

Feedback

This question depicts chromosomes and asks which pair represents an Autosomal
Recessive inheritance pattern. Each of the chromosomes are pictured carrying an allele
from each parent, which is depicted by a yellow or green box. The green box
represents a normal or dominant allele, while the yellow box represents a mutant or
recessive allele.
An Autosomal trait will be carried on a numbered chromosome and both chromosomes
should have the same number. An X-linked trait will be carried on an X-chromosome.
This allows us to rule out answer choices A and B.

To inherit a recessive trait, we need to inherit two recessive (or mutant alleles), which
would be shown as two yellow boxes. A dominant trait can be inherited when one or
two dominant alleles are present. Answer choice C depicts an Autosomal Dominant
inheritance, while answer choice D is the correct answer because it depicts an
Autosomal Recessive inheritance pattern.

Hemophilia is an X-linked recessive condition. This means that:

1. A person with at least one normal X chromosome without the hemophilia gene will
not show signs of hemophilia
2. The disease is more common in females
3. Affected men can pass the condition on to sons but not to daughters
4. Women can only pass the condition on to daughters - 1. A person with at least one
normal X chromosome without the hemophilia gene will not show signs of hemophilia

Feedback
An X-linked recessive condition is inherited when a female has a recessive allele on
each of her X chromosomes. Males inherit an X-linked recessive condition if they
inherit a recessive allele on their one and only X chromosome. Therefore if a female
has a dominant (or normal) allele on one of her X chromosomes, she will not have the
disease.
Because men only have one X-chromosome, they tend to inherit X-linked conditions
more easily than females.

Men with X-linked recessive conditions do not pass the disease on to their sons,
because they pass a Y chromosome on to their sons. Men will pass an X chromosome
to their daughters.

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