Genetics Chpt. 12 and 13 Flashcards

1
Q

How many bands of DNA would be expected in
Meselson and Stahl’s experiment after two rounds
of conservative replication?

A

two

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2
Q

Replicons

A

units of replication

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3
Q

Conservative Replication

A

one is entirely new DNA, and the other is made of old DNA strands

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4
Q

Dispersive Replication

A

the original DNA double helix breaks apart into fragments, and each fragment then serves as a template for a new DNA fragment

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5
Q

Semi-Conservative Replication

A

every new DNA double helix would be a hybrid that consisted of one strand of old DNA bound to one strand of newly synthesized DNA

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6
Q

Theta

A

circular DNA, no break in nucleotide strand, 1 replicon, unidirectional/bidirectional

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7
Q

Rolling-Circle

A

circular DNA, break in nucleotide strand, 1 replicon, unidirectional

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8
Q

Linear Eukaryotic

A

linear DNA, no break in nucleotide strand, many replicons, bidirectional

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9
Q

Which type of replication requires a break in the
nucleotide strand to get started?

A

Rolling-Circle Replication

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10
Q

Requirements for DNA Replication

A

template strand, nucleotides, enzymes and other proteins

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11
Q

DNA replication takes place in a

A

semiconservative model

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12
Q

Replication runs from

A

5’ to 3’

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13
Q

Nucleotides get added to what end

A

3’

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14
Q

Leading Strand

A

undergoes continuous replication

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15
Q

Lagging Strand

A

undergoes discontinuous replication

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16
Q

Okazaki Fragments

A

discontinuously synthesized
short DNA fragments forming the lagging strand

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17
Q

Discontinuous replication is a result of which
property of DNA?

A

antiparallel nucleotide strands

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18
Q

Place the following components in the order in
which they are first used in the course of
replication:
helicase
single-strand-binding protein
DNA gyrase
initiator protein

A

initiator protein, helicase, single-strand-binding protein, DNA gyrase

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19
Q

Primers

A

an existing group of RNA nucleotides with a
3’-OH group to which a new nucleotide can be
added; they are usually 10–12 nucleotides long

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20
Q

Primase

A

RNA polymerase…synthesize primers with a 3’-OH group at the beginning of each DNA fragment

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21
Q

Primers are synthesized where on the lagging
strand?

A

at the beginning of every okazaki fragment

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22
Q

Helicase

A

unwinds the DNA

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23
Q

Single-Strand-Binding Proteins

A

protect the single nucleotide strands and prevent secondary structures

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24
Q

DNA Gyrase

A

remove strain ahead of the replication fork

25
DNA Polymerase I
removes and replaces primers
26
DNA Polymerase III
carries out elongation
27
Ligase
connects nicks (Okazaki fragments) after RNA primers are removed
28
Termination
when the replication fork meets or by a termination protein
29
DNA Polymerase II
DNA repair; restarts replication DNA; halts synthesis
30
DNA Polymerase IV
DNA repair
31
DNA Polymerase V
DNA repair; translesion DNA synthesis
32
Polymerase generally
synthesized the leading and lagging strands
33
Which bacterial enzyme removes the primers?
DNA polymerase I
34
Proofreading
DNA polymerase I: 3' - 5' exonuclease activity removes the incorrectly paired nucleotide
35
Mismatch Repair
corrects errors after replication is complete
36
Which mechanism requires the ability to distinguish between newly synthesized and template strands of DNA?
mismatch repair
37
In comparison with prokaryotes, what are some differences in the genome structure of eukaryotic cells that affect how replication takes place?
The size of eukaryotic genomes, the linear structure of eukaryotic chromosomes, and the association of DNA with histone proteins
38
Some of the eukaryotic DNA polymerases have a tendency to make errors in replication. Why would a cell use an error-prone DNA polymerase instead of one that is more accurate?
Error-prone DNA polymerases can bypass lesions in the DNA helix that stall accurate, high-speed DNA polymerases
39
What would be the result if an organism’s telomerase were mutated and nonfunctional?
Chromosomes would shorten each generation
40
Why is recombination important?
Recombination is important for genetic variation and for some types of DNA repair.
41
What is the function of resolvase in recombination?
It cleaves the Holliday structure
42
Ribozymes
catalytic RNA
43
Ribosomal RNA (rRNA)
structural and functional components of the ribosome
44
Messenger RNA (mRNA)
carries genetic code for proteins
45
Transfer RNA (tRNA)
helps incorporate amino acids into polypeptide chain
46
Transcription requires
DNA template, raw materials (ribonucleotide triphosphates), transcription apparatus
47
Transcribed strand is
template strand
48
The transcription unit is composed of
a promoter, RNA-coding sequence, and terminator
49
What is the difference between the template strand and the nontemplate strand?
The template strand is the DNA strand that is copied into an RNA molecule, whereas the nontemplate strand is not copied
50
Which of the following phrases does NOT describe a function of the promoter?
signals where transcription ends
51
Sigma Factor
binding to the promoter when transcription starts
52
In transcription, nucleotides are added to the
3' end
53
What is the function of the sigma factor?
The sigma factor controls the binding of RNA polymerase to the promoter
54
What binds to the −10 consensus sequence found in most bacterial promoters?
holoenzyme (core enzyme + sigma factor)
55
What characteristics are most commonly found in rho-independent terminators?
inverted repeats followed by a string of adenine nucleotides
56
The promoters of genes transcribed by RNA polymerase II consists of two primary parts
a core promoter and a regulatory promoter
57
What is the difference between the core promoter and the regulatory promoter?
Both b and c above
58
What is the role of TFIID in transcription initiation?
RNA polymerase over the transcription start site
59
How are the processes of RNA polymerase II termination in eukaryotes and rho-dependent termination in bacteria similar, and how are they different?
Both processes use a protein that binds to the RNA molecule and moves down the RNA toward the RNA polymerase. They differ in that rho does not degrade the RNA, whereas Rat1 does.