First Aid Biochem_Genetics Part I Flashcards

(50 cards)

1
Q

1 Text

A

2 Text

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2
Q

Which histone # is the linker?

A

H1

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3
Q

Which histone #s are the nucleosome core?

A

H2A, H2B, H3, H4

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4
Q

Is euchromatin or heterochromatin more transcriptionally active?

A

Euchromatin is active; hetero is inactive

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5
Q

What three amino acids are required for purine synthesis?

A

Glycine, aspartate, glutamine

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6
Q

Is orotic acid a purine or pyrmidine precursor?

A

Pyrmidine

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7
Q

What does a degenerate genetic code mean?

A

More than one codon codes for the same amino acid

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8
Q

What is a nonsense vs a missense mutation?

A

Nonsense = STOP codon, missense = substitute one amino acid for another

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9
Q

Do eukaryotes have a single or multiple origin of replication?

A

Multiple

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10
Q

What does primase do?

A

Makes RNA primer on which DNA pol III can initiate replication

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11
Q

What does DNA pol I do?

A

Degradees RNA primer and fills in gap with DNA

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12
Q

What does DNA pol III do?

A

Adds deoxynulceotides to 3’ end; has internal proofreading actiivty. Replication!

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13
Q

What type of exonuclease activity does DNA pol III have?

A

3’ to 5’; proofreads

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14
Q

What does DNA ligase do?

A

Connects Okazaki fragments together

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15
Q

What is nucleotide excision repair? In what disease is it defective?

A

Endonucleases remove damaged bases; ex xeroderma pigmenteosum

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16
Q

What is base excision repair?

A

Specific glycosylases remove damaged bases, AP endonuclease cuts DNA at apyrimidinic site, empty sugar removed

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17
Q

What is mismatch repair? In what disease is it defective?

A

Unmethylated, newly synthesized sring is recognized, mismatched nucleotides are removed, gap is resealed; HNPCC

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18
Q

What is nonhomologous end joining? In what disease is it defective?

A

Double stranded DNA repair; brings 2 ends of DNA together; ataxia telangiectasias

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19
Q

Is protein synthesis from C to N or N to C?

A

N to C

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20
Q

In what direction is mRNA read?

A

5’ to 3’

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21
Q

What type of RNA is the most abundant?

22
Q

What is the start codon?

23
Q

What are three mRNA stop codons?

A

UGA, UAA, UAG

24
Q

Where are silencers and enhancers found on the chromosome?

A

Close, far away, or within; they can be upstream or downstream from a gene

25
What are two upstream promotor sequences?
TATA and CAAT boxes
26
What does rRNA pol I, II, and III do?
I = rRNA, II = mRNA, III = tRNA
27
What substance can inhibit RNA pol II?
Alpha-amanitin
28
What are there processes that occur to convert pre-mRNA to mature mRNA?
1. 5' 7-methylguanosine cap, 3' polyadenylation, splicing of introns
29
What is the polyadenylation signal sequence?**
AAUAAA
30
What two enzymes do not require a template to transcribe DNA?
Poly-A polymerase, telomerase
31
What disease is associated with antibodies to spliceosomal snRNPs?
SLE
32
Where does a repressor bind in the lac operon?
Operator
33
What compound inhibits the repressor in the lac operon?
Lactose
34
What compound inhibits the activator in the lac operon?
Glucose via decreased cAMP
35
Are exons/introns the coding or noncoding sequences?
Exons are EXPRESSED, introns are INTERVENING
36
What disease has mutations of the introns?
beta-thalassemias
37
Is the CCA sequence on the 3' or 5' end of tRNA?
3'
38
What does the CCA sequence do?
Covalently binds the amino acid
39
What enzyme is responsible for tRNA charging?
Aminoacyl-tRNA synthetase
40
What enzyme is responsible for proofreading tRNA charging?
Aminoacyl-tRNA synthetase
41
What is the wobble effect?
3rd nucleotide of the codon can vary, due to degeneracy of the genetic code
42
What is the energy source for protein synthesis initiation?
GTP
43
What is the energy source for tRNA charging? tRNA translocation?
ATP and GTP respectively
44
Which aminoacyl-tRNA does NOT bind to the A site first?
AUG/methionine; binds to P site first
45
What antibiotic inhibits moving tRNA from the A site to the P site?
Macrolides (translocation!)
46
What antibiotic can cause misreading of mRNA?
Aminoglycosides
47
What is the role of ubiquitination?
Targets proteins for degredation in proteosome
48
What are the major tumor supressors for the G1 to S phase tranistion?
p53 and RB
49
What cells are considered quiescent (in that they can move from G0 to G1 if provoked)
Hepatocytes, lymphocytes
50
What are labile cells?
Never go into G0; ex bone marrow, gut epithelium, skin, hair follicles