unit 1 key area 2 Flashcards

(21 cards)

1
Q

when does DNA replication occur

A

before a cell divides

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2
Q

what does DNA replication ensure

A

an exact copy of a species genetic information is passed on from one cell to another during growth

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3
Q

what are the requirements for DNA replication

A

DNA, primers, nucleotides, DNA polymerase, DNA ligase and ATP

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4
Q

what is a primer

A

a short strand of nucleotides that binds to the 3’ end of the template allowing polymerase to add nucleotides

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5
Q

what is DNA polymerase

A

enzyme which adds nucleotides. it can only add complimentary nucleotides in one direction to the 3’ end

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6
Q

what is DNA ligase

A

joins fragments of the lagging strand

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7
Q

what is stage 1 of DNA replication

A

DNA is unwound (by DNA
Polymerase) and weak hydrogen bonds between bases
break to form 2 template strands.

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8
Q

what is the point of separation called

A

replication fork

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9
Q

what is stage 2 of DNA replication

A

a primer attaches to the 3’ end of the strand of to be replicated by DNA polymerase

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10
Q

what is stage 3 of DNA replication

A

DNA polymerase can now add free complimentary nucleotides to the 3’ end of the primer and the new (leading) strand forms continuously

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11
Q

what is stage 4 of DNA replication

A

the opposite strand is replicated in fragments as the DNA strand unzips. this is called the lagging strand

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12
Q

what is stage 5 of DNA replication

A

DNA ligase joins the fragments on the lagging strand

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13
Q

what is PCR

A

when DNA fragments are amplified through repeated cycles of artificial replication using complementary primers for specific target sequences.

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14
Q

what happens to the number of DNA fragments after one cycle

A

it doubles

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15
Q

what does the process of PCR involve

A

cycles of heating and cooling which amplifies the target region of DNA

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16
Q

what is required for PCR

A

heat tolerant DNA polymerase, DNA template, primers, pH buffer and 4 types of DNA nucleotide

17
Q

what is stage 1 of PCR

A

double stranded fragment heated to 92/98 degrees to break hydrogen bonds between bases and separate the two strands

18
Q

what is stage 2 of PCR

A

the now separated strands are cooled to 50/65 degrees to allow primers to anneal to complimentary target sequence

19
Q

what is stage 3 or PCR

A

it is now heated to 70/80 degrees so heat tolerant DNA polymerase can replicate the region of DNA by adding primers to 3’ end

20
Q

what happens after stage 3 of PCR

A

the cycle is repeated

21
Q

what are the practical applications of PCR

A
  1. forensics - analyse minute traces of blood/other tissues
  2. diagnostically - diagnosis of genetic diseases/disorders
  3. paternity suits - to identify the father of a child