Exam 3 review Flashcards

1
Q

What are the three ways in which RNA polymerase “scans” the bacterial genome?

A

Sliding, Intersegmental transfer, and Intrasegmental transfer

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2
Q

Mutations in sigma factor’s DNA binding domain are unlikely to change its affinity for hexameric promoter elements.

A

False

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3
Q

During abortive initiation nascent RNA approximately ________ long is synthesized and the RNA polymerase holoenzyme ________ change locations.

A

9 base; does not

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4
Q

The positioning factor for RNA polymerase III is:

A

TFIIIB

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5
Q

Which features define a transcription factor?

A

it must bind DNA in a sequence specific manner,it must be a protein, and it must participate in transcriptional regulation

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6
Q

During transcriptional initiation a ternary complex is formed comprising of:

A

RNA polymerase holoenzyme, nascent RNA, and template DNA

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7
Q

DNA repair and transcription can be coupled, which of the following factors participates in both DNA repair and transcription.

A

TFIIH

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8
Q

An RNA polymerase III type 1 promoter contains which cis elements:

A

boxA, boxC

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9
Q

Recognizing and binding to the translational start site is a function of __________.

A

the small ribosomal unit

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10
Q

Translational elongation is a GTP dependent mechanism.

A

True

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11
Q

Fusion of FokI to a TALE protein provides the nuclease activity in a TALEN

A

True

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12
Q

How many different types of RNA polymerases can be found in E. coli?

A

1

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13
Q

Enhancer elements are almost always upstream of the minimal promoter.

A

False

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14
Q

Sigma factor binding to the core enzymes causes a conformational change that ________ the connection between the holoenzyme and the template strand.

A

increases

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15
Q

Where does a formylated methionine-tRNAf enter the ribosome?

A

P-site

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16
Q

A start point in a bacterial or eukaryotic promoter is almost always a (an) ______ ?

A

purine

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17
Q

RNA polymerase I is primarily active in the ________.

A

nucleolus of a eukaryotic nucleus

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18
Q

CpG islands in eukaryotic genomes may be the target of methylation. The result of CpG methylation in the promoter region of a structural gene will most likely ________________ .

A

inhibit transcription of a gene

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19
Q

Fluorescently labeled chain terminating dideoxynucleotides are used in:

A

Sanger sequencing

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20
Q

A rut site is a target for ________ binding?

A

Rho factor

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21
Q

Dead Cas9 (dCas9) retains nuclease activity but cannot bind to target DNA.

22
Q

Which major cis element is consistently contained in an RNA polymerase II promoter?

23
Q

During promoter binding and initiation sigma factor physically interacts with the RNA polymerase core enzymes and the promoter sequence.

24
Q

Which mechanism for finding and removing “bad” mRNA takes its signal from the presence of a premature termination codon and an unusually lengthy 3’UTR?

A

nonsense mediated decay

25
EF-Tu and EF-G can occupy the same A-site simultaneously.
False
26
Sigma factor always disassociates from the holoenzyme enzymes before elongation can proceed.
False
27
Which is true about a protospacer?
protospacer represents a target sequence in the CRISPR system
28
In E. coli RNA polymerase is most often found associated with DNA.
True
29
Deoxyribonucleoside triphosphates are required for RNA synthesis.
False
30
Partner proteins in transcription may or may not transcription factors.
True
31
TBP must bind the TATA-box
False
32
Intrinsic termination relies on cis acting factors.
True
33
Which cis elements comprise a bacterial promoter?
Pribnow box and -35 box
34
The simplest and most cost-effective method for detecting the presence or absence of a specific DNA sequence is quantitative Realtime PCR.
False
35
Where does an aminoacyl-tRNA enter the ribosome?
A-site
36
What are the two primary mechanisms for transcriptional termination in prokaryotes?
Rho dependent termination and Intrinsic termination
37
A gene drive only moderately increases the inheritance of the selfish allele above typical Mendelian pattern of inheritance.
False
38
The terminator sequence that instructs bacterial RNA polymerase to cease transcription is only part of the DNA template sequence.
False
39
The bacterial RNA polymerase holoenzyme is a complex of:
α2ββ'ωσ
40
In eukaryotes, RNA polymerase is responsible for locating and binding to the core promoter without aid from other factors.
False
41
In transcription, assembly factors are directly responsible for _________ .
positioning the positioning factors at the promoter
42
Enhancer elements are always required for RNA polymerase II transcription.
False
43
CRISPR is an acronym for...
clustered regularly interspaced short palindromic repeat
44
Using Cas9 nickase (nCas9) can improve genome editing specificity by requiring a second Cas9 target for DNA double strand cleavage.
True
45
Nonsense mediated decay can be bypassed by artificial addition of a PABP site immediately downstream of the premature termination codon.
True
46
In genome editing an off-target effect is a consequence of editing the wrong sequence.
True
47
What protein is part of all positioning factors?
TATA binding protein
48
In a mammalian cell, what proportion of total RNA is ribosomal RNA (rRNA)?
70%
49
An RNA polymerase III type 3 promoter contains which cis elements:
PSE, Oct, TATA-box
50
What would one expect if the NTD (N-terminal domain) of σ70 is deleted in a bacterium?
σ70 would stick to DNA even in the absence of the RNA polymerase core enzyme.
51
Sigma factor is required for transcriptional initiation but not elongation.
True