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WGU C785 Final Exam 2024 Questions With Complete Solutions(Guaranteed Success)

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WGU C785 Final Exam 2024 Questions With Complete Solutions(Guaranteed Success) Hemophilia Pedigree - Father has hemophilia, mother does not. What is the outcome for their kids? - correct ans...His daughters would be carriers. This is x-link recessive. Autosomal: Dominant: - correct ans...Autosomal: males and females equally affected. Dominant: non-carrier parents polymerase chain reaction (PCR) - correct ans...The process of copying DNA in the lab. Uses Template DNA, Nucleotides (dNTPS), DNA Polymerase, and DNA primers. 3 Steps of PCR - correct ans...1. Denaturation: DNA is heated to 95C to separate it. 2. Annealing: reaction is cooled to 50C; primers stick to the DNA you want to copy and add DNA polymerase. 3. Elongation: reaction heated to 70C and DNA polymerase, adding nucleotides building a new DNA strand. Base Excision Repair (BER) - correct ans...How you repair a mutation. BER is used to repair damage to a base caused by harmful molecules. You remove the base that is damaged and replace it. *BER removes a single nucleotide* DNA glycolsylase - sees damaged DNA and removes it. DNA polymerase-puts the right one back in while DNA ligase seals it. Mismatch repair (MMR) occurs during: - correct ans...replication. DNA polymerase proofreads but sometimes a mismatch pair gets through. MMR removes a large section of the nucleotides from the new DNA and DNA polymerase tries again. (Ex: C-T instead of C-A) Mismatch Repair corrects what kind of DNA damage? - correct ans...When a base is mismatched due to errors in replication. Such as G-T instead of G-C. DNA polymerase comes by and fixes it. What happens when DNA polymerase binds to DNA to make RNA? - correct ans...TRANSCRIPTION! DNA polymerase takes the individual nucleotides and matches them to the parental sequences to ensure a correct pair. It must bind with RNA primer to work. What is needed for DNA replication? - correct ans...DNA polymerase Nonsense Mutation - correct ans...Change in 1 nucleotide produces a STOP codon Stop= nonsense because it is no more. Silent Mutation - correct ans...Change in 1 nucleotide but codes for the same amino acid. Silent= the change doesn't change the name of the protein Missense Mutation - correct ans...Change in 1 nucleotide leads to a code for a different amino acid. Missense = mistake was made. What happends during RNA splicing? - correct ans...During RNA splicing introns are cut out, the remaining exons are joined together. 5'ATG AGT CTC TCT 3' Find the DNA template strand. - correct ans...3'TAC TCA GAG AGA 5' The DNA template strand is complimentary. So start with the opposite number, then go L-R with the complimentary letter. 5'ATG AGT CTC TCT 3' What is the corresonding mRNA sequence? - correct ans...5'AUG AGU CUC UCU 3' This sequence is the same as the coding strand except T changes to U because it is RNA. RNA doesn't have T. How would a mutation from CTC to ATC affect the protein sequence? (CTC/ATC - coding strand, AUC - mRNA strand) - correct ans...This will make a missense mutation because it changes the name of the protein. (look at the chart provided.) missense = mistake DNA replication process - correct ans...DNA ->Transcription -> RNA -> Translation -> Polypeptide Describe how you would find what ionized Alanine looks like. - correct ans...This is an amino acid. Look for the "R" group. Alanine is a hydrophobic amino acid that has CH3. It is a weak interaction. An ionized acid will have a + or - charge. Describe what causes the misfolding of protein in Alzheimer's Disease. - correct ans...Protein misfolding is caused by intracellular tangles and extracellular plaques (senile plaques) caused by abnormal protein aggregation. TAU is fibrous material inside cells where the connections are lost. This becomes defective and forms filaments in the neuron. Amyloid-Beta is a large precursor protein in the cell. Excess amyloid-beta creates senile plaques. This starts in the hippocampus and moves up. Describe the process of neurodegenerative protein aggregation. - correct ans...Alzheimer's is the most common neurodegenerative disease. The formation of aggregated amyloid-beta fibers is another characterisitc of Alzheimer's. However, neurodegeneration and memory loss can be detected before amyloid fibers accumulate in the brain. What are the molecules that help denatured proteins with folding? - correct ans...Molecular chaperones are protein helpers. They bind to the newly made polypeptide and enable proper folding. Proper protein folding is vital b/c proteins that do not fold properly can lead to a variety of diseases. Normally, the chaperones that help new proteins fold can also help misfolded proteins refold into the correct structure. Genetic mutations that substitute one amino acid for another can cause incorrect folding. What are the 4 levels of protein structure? - correct ans...1. Primary-chain of amino acids. PEPTIDE bonds form a polypeptide chain. This is a covalent bond (very strong) and does not denature. 2. Secondary-alpha helix and beta sheet. HYDROGEN bonds that contain the carboxyl group and amino groups. Denatured by salt and pH change. 3. Tertiary-side chain interaction (R group). Changes are seen with high temp, salt, change in pH, and reducing agents. (ex: sickle cell, arthritis, hemophilia) 4. Quarternary-more than 1 polypeptide. Change seen with increased temp. (Ex: Hgb) Hydrogen bonds are formed from - correct ans...2 polar amino acids. (Contains Oxygen and nitrogen-OH, NH, NH2. On exterior surface) What structure would be unaffected by complete denaturation of its multi-subunit? - correct ans...PRIMARY. Peptide bonds are strong and covalent. The primary structure is located at the backbone and does not denature. What is the simplest way to denature a protein? - correct ans...Heat it up. The tertiary structure is hydrophobic. The tertiary structure is a protein structure stabilized primarily by the hydrophobic effect. What is the secondary structure made up of? - correct ans...Alpha helixes and beta sheets Describe what is meant by "induced fit" of a substrate and enzyme. - correct ans...The substrate and active site are somewhat complementary prior to substrate binding. Many enzymes will adjust their active site conformation slightly as the substrate binds to improve the fit. When the molecule is recognized as the substrate, the enzyme will adjust to form itself around the substrate more tightly to facilitate the reaction it catalyzes.

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Course BioChem C785
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Uploaded on
July 31, 2024
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Written in
2023/2024
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WGU C785 Final Exam 2024 Questions With Complete
Solutions(Guaranteed Success)

Hemophilia Pedigree - Father has hemophilia, mother does not. What is the outcome for
their kids? - correct ans...✔✔His daughters would be carriers. This is x-link recessive.

Autosomal:
Dominant: - correct ans...✔✔Autosomal: males and females equally affected.
Dominant: non-carrier parents

polymerase chain reaction (PCR) - correct ans...✔✔The process of copying DNA in
the lab. Uses Template DNA, Nucleotides (dNTPS), DNA Polymerase, and DNA
primers.

3 Steps of PCR - correct ans...✔✔1. Denaturation: DNA is heated to 95C to separate it.
2. Annealing: reaction is cooled to 50C; primers stick to the DNA you want to copy and
add DNA polymerase.
3. Elongation: reaction heated to 70C and DNA polymerase, adding nucleotides building
a new DNA strand.

Base Excision Repair (BER) - correct ans...✔✔How you repair a mutation. BER is used
to repair damage to a base caused by harmful molecules. You remove the base that is
damaged and replace it. *BER removes a single nucleotide*
DNA glycolsylase - sees damaged DNA and removes it.
DNA polymerase-puts the right one back in while DNA ligase seals it.

Mismatch repair (MMR) occurs during: - correct ans...✔✔replication. DNA polymerase
proofreads but sometimes a mismatch pair gets through. MMR removes a large section
of the nucleotides from the new DNA and DNA polymerase tries again. (Ex: C-T instead
of C-A)

Mismatch Repair corrects what kind of DNA damage? - correct ans...✔✔When a base
is mismatched due to errors in replication. Such as G-T instead of G-C. DNA
polymerase comes by and fixes it.

What happens when DNA polymerase binds to DNA to make RNA? - correct ans...✔✔
TRANSCRIPTION! DNA polymerase takes the individual nucleotides and matches them
to the parental sequences to ensure a correct pair. It must bind with RNA primer to
work.

What is needed for DNA replication? - correct ans...✔✔DNA polymerase




A GRADESOLUTIONS

, Nonsense Mutation - correct ans...✔✔Change in 1 nucleotide produces a STOP codon
Stop= nonsense because it is no more.

Silent Mutation - correct ans...✔✔Change in 1 nucleotide but codes for the same amino
acid. Silent= the change doesn't change the name of the protein

Missense Mutation - correct ans...✔✔Change in 1 nucleotide leads to a code for a
different amino acid. Missense = mistake was made.

What happends during RNA splicing? - correct ans...✔✔During RNA splicing introns
are cut out, the remaining exons are joined together.

5'ATG AGT CTC TCT 3'
Find the DNA template strand. - correct ans...✔✔3'TAC TCA GAG AGA 5'
The DNA template strand is complimentary. So start with the opposite number, then go
L-R with the complimentary letter.

5'ATG AGT CTC TCT 3'
What is the corresonding mRNA sequence? - correct ans...✔✔5'AUG AGU CUC UCU
3'
This sequence is the same as the coding strand except T changes to U because it is
RNA. RNA doesn't have T.

How would a mutation from CTC to ATC affect the protein sequence? (CTC/ATC -
coding strand, AUC - mRNA strand) - correct ans...✔✔This will make a missense
mutation because it changes the name of the protein. (look at the chart provided.)
missense = mistake

DNA replication process - correct ans...✔✔DNA ->Transcription -> RNA -> Translation
-> Polypeptide

Describe how you would find what ionized Alanine looks like. - correct ans...✔✔This is
an amino acid. Look for the "R" group. Alanine is a hydrophobic amino acid that has
CH3. It is a weak interaction. An ionized acid will have a + or - charge.

Describe what causes the misfolding of protein in Alzheimer's Disease. - correct ans...✔
✔Protein misfolding is caused by intracellular tangles and extracellular plaques (senile
plaques) caused by abnormal protein aggregation.
TAU is fibrous material inside cells where the connections are lost. This becomes
defective and forms filaments in the neuron.
Amyloid-Beta is a large precursor protein in the cell. Excess amyloid-beta creates senile
plaques. This starts in the hippocampus and moves up.

Describe the process of neurodegenerative protein aggregation. - correct ans...✔✔
Alzheimer's is the most common neurodegenerative disease. The formation of


A GRADESOLUTIONS

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