Written by students who passed Immediately available after payment Read online or as PDF Wrong document? Swap it for free 4.6 TrustPilot
logo-home
Document preview thumbnail
Preview 3 out of 18 pages
Exam (elaborations)

WGU 785 Final Exam QUESTIONS WITH CORRECT EXPERT VERIFIED ANSWERS

Document preview thumbnail
Preview 3 out of 18 pages

WGU 785 Final Exam QUESTIONS WITH CORRECT EXPERT VERIFIED ANSWERS Hemophilia Pedigree - Father has hemophilia, mother does not. What is the outcome for their kids? – His daughters would be carriers. This is x-link recessive. Autosomal: Dominant: - Autosomal: males and females equally affected. Dominant: non-carrier parents polymerase chain reaction (PCR) – The process of copying DNA in the lab. Uses Template DNA, Nucleotides (dNTPS), DNA Polymerase, and DNA primers. 3 Steps of PCR – 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) – 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 polymeraseputs the right one back in while DNA ligase seals it. Mismatch repair (MMR) occurs during: - 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)

Content preview

lOMoAR cPSD| 22830792




WGU 785 Final Exam
QUESTIONS WITH CORRECT
EXPERT VERIFIED ANSWERS
Hemophilia Pedigree - Father has hemophilia, mother does not. What is the outcome for
their kids? –

His daughters would be carriers. This is x-link recessive.

Autosomal:

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

polymerase chain reaction (PCR) –

The process of copying DNA in the lab. Uses Template DNA, Nucleotides
(dNTPS), DNA Polymerase, and DNA primers.

3 Steps of PCR –

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) –

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: -

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)

, lOMoAR cPSD| 22830792




Mismatch Repair corrects what kind of DNA damage? –

, lOMoAR cPSD| 22830792




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? –

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? –

DNA polymerase

Nonsense Mutation –

Change in 1 nucleotide produces a STOP codon Stop= nonsense because it is no
more.

Silent Mutation –

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

Missense Mutation –

Change in 1 nucleotide leads to a code for a different amino acid. Missense =
mistake was made.

What happends during RNA splicing? –

During RNA splicing introns are cut out, the remaining exons are joined together.

5'ATG AGT CTC TCT 3'
Find the DNA template strand. –

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? –

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.

Document information

Uploaded on
November 19, 2023
Number of pages
18
Written in
2023/2024
Type
Exam (elaborations)
Contains
Questions & answers
$10.99

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
Sold
200
Followers
119
Items
2810
Last sold
2 weeks ago



Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions