DNA replication (Genetics 4) Flashcards

1
Q

What must a cell do to divide?

A

Grow, copy its genetic material and split into two daughter cells

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2
Q

What two major phases is the cell cycle divided into?

A

Interphase and mitotic phase

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3
Q

What occurs during interphase

A

the cell grows and makes a copy of its DNA

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4
Q

What occurs during the mitotic phase

A

the cell separates its DNA into two sets and divides its cytoplasm, forming two new cells

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5
Q

Semi-conservative replication

A

DNA acts as a template for its own replication

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6
Q

DNA Helicase

A

breaks the hydrogen bonds between nucleotides

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7
Q

DNA Polymerase

A

synthesises DNA in the 5 to 3 direction

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8
Q

DNA Topoisomerase

A

relieves tension in the DNA

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9
Q

DNA Primase

A

syntheises RNA primers

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10
Q

Ribonucleases

A

degrades RNA Primers

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11
Q

DNA Ligase

A

joins DNA fragments

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12
Q

Telomerase

A

replicates the ends of the chromosome

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13
Q

Single-Strand Binding Protein

A

Binds and keeps both strands apart from each other

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14
Q

Leading Strand

A

Continuous DNA production

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15
Q

Lagging Strand

A

Discontinuous DNA production

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16
Q

Okazaki fragments

A

short DNA sequences produced on the lagging strand

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17
Q

Sliding clamp

A

Ring shaped protein, binds DNA polymerase to the DNA template

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18
Q

DNA primase

A

Found on the lagging strand, attaches RNA to the template

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19
Q

DNA polymerase III

A

adds nucleotides until it reaches the previous primer

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20
Q

RNase H

A

digests the RNA primer, leaving a gap

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21
Q

DNA polymerase

A

fills in the gaps between two okazaki fragments

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22
Q

DNA ligase

A

Joins two fragments together on the lagging strand

23
Q

Telomeres

A

Repetitive units at the end of chromosomes

24
Q

Function of Telomeres

A

Protect the internal regions of the chromosomes/ worn down during DNA replication

25
DNA polymerase A
doesn't require a primer, has its own primase enzyme- therefore preventing the shortening of the DNA strand
26
How can DNA become damaged?
UV light, ionising radiation, toxic chemical agents, reactive oxygen
27
Double stranded breaks
Chromosomes split into two caused by environmental factors such as high energy radiation
28
Gain of function
Change in DNA that leads to increased/ alternative activity
29
Loss of Function
Change in DNA that leads to decreased activity
30
Splice-site mutation
A splice site mutation is a genetic mutation that inserts, deletes or changes a number of nucleotides in the specific site at which splicing takes place
31
Excision
the first stage of mechanism of DNA repair; recognition and removal of damage (exonuclease)
32
Repair
The second stage of DNA repair-synthesis of missing DNA (DNA polymerase)
33
Joining
The final stage of DNA repair, sealing the fragments (DNA Ligase)
34
Thymine Dimers
Two Thymine Bases become covalently bonded to each other
35
What is the difference between DNA polymerase III and DNA polymerase I
DNA polymerase III: Synthesises the nucleotides on the lagging strand DNA polymerase I: fills in the gaps
36
What is Depurination?
DNA mutation, removal of an Adenine or Guanine base
37
What is Deamination?
DNA mutation, removal of ammonia changing cytosine to Uracil
38
What do Thymine Dimers arise from?
UV radiation
39
What is nonsense mediated decay?
a process during translation that detects transcripts with premature stop codons and degrades them.
40
What direction is DNA usually synthesised in?
5' to 3' direction
41
What is a primer?
A short section of RNA
42
How often does DNA polymerase make a mistake?
once every 10 to the 7 nucleotide pairs
43
What are the 3 different point mutations?
Silent, Missense and Nonsense
44
What is Nonsense Mediated Decay?
a process during translation that detects transcripts with premature stop codons and degrades them.
45
What factors effect whether an indel mutation will be tolerated?
Whether it's a frameshift, its size and its location
46
What is a splice site mutation?
A genetic mutation that changes the number of nucleotides at the area where splicing occurs
47
What is non-homologous end joining?
The ends are ‘polished’ to produce ‘blunt ends’ » The ends are then joined (DNA ligase)
48
What is the problem with non-homologous end joining?
there will be a resultant loss in nucleotides, the consequence depends on its position within the genome
49
When is non-homologous end joining usually used?
for rapidly dividing cells
50
Homologous end joining
recombination between two corresponding regions of the two alleles, it is a complete repair which means that no sequences are lost
51
What is the problem with homologous end joining?
It is much more slower and therefore less useful for rapidly dividing cells but it is much more accurate
52
What is a conservative substitution?
similar amino acid R group and size
53
What is a radical substitution?
New amino acid R group that is different in charge and size