Introduction to Bio 2 Flashcards

1
Q

How do DNA strands run

A

antiparallel

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2
Q

DNA theories

A
semiconservative = strands unwound and each daughter has one new and one old
conservative = strands unwound and one completely new one is made and the original
Dispersive = strands are used alternatively
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3
Q

Whats the main evidence for these models

A

1958: Mathew meselson and Frank Stahls experiment

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4
Q

Whats the replication rate

A

2 kb/minute, initiates at many different sites simultaneously

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5
Q

growing strand is in what direction

A

5 to 3

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6
Q

Where are phosphate groups bound

A

the 5 end hydroxyl group of nucleotide attacks 3 hydroxy group at end of the chain

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7
Q

Lagging strand

A

synthesised in short fragments

RNA primer required

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8
Q

Where is DNA primase found

A

animals cells

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9
Q

Where is RNA primase

A

in bacteria

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10
Q

Whats the role of telomerase

A

provides a mechanism to extend the template until its long enough for normal lagging strand synthesis

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11
Q

What is the genetic sequence for telomeres

A

TTAGGG

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12
Q

Where are telomeres active

A

in stem cells and actively proliferating cells

less active in somatic cells - ageing

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13
Q

When are errors removed

A

during synthesis

mutations can also be removed post-replicatively

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14
Q

What percentage of mistakes are caught by proofreading exonuclease associated with polymerase

A

99.9%

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15
Q

What is the overall mutation rate

A

10^10

1 error every 3 genomes replicated

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16
Q

Steps in using PCR in determining infectious agents

A

-blood sample
-remove cells via centrifugation
-rare HIV particile in serum of infected person
-extract viral RNA genome
-Reverse transcriptase/PCR amplification
-Gel electrophoresis
(control using blood from non-infected person)

17
Q

What is a short tandem repeat

A

micro satellite

18
Q

What is Short Tandem Repeat (STR) analysis used for

A

compare specific loci on dna

19
Q

What is the function of Quantitive Fluorescent PCR (QF-CPR)

A

Amplifies short-tandem repeats unique to each chromosome

-can have a 2:1 ratio of alleles or 3 alleles

20
Q

What protein is present in Alexander disease

A

glial fibrillary acidic protein (GFAP)

21
Q

Symptoms of Alexander disease

A

slow progressing neurodegeneration

defective myelin sheath

22
Q

What is the name of the thing that can’t replicate

A

Dideoxyribonucleoside triphosphate