Molecular Biology (W12) Flashcards

1
Q

define penetrance and expressivity

A

penetrance : % of individuals that express the phenotype

expressivity : degree to which the trait is expressed

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2
Q

what is the difference between a ribose and deoxyribose sugar

A

ribose: OH group on carbon 2

deoxyribose : H group on carbon 2

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3
Q

how many hydrogen bonds form between each of the base pairs

A

A + T form 2 H bonds
C + G form 3 H bonds

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4
Q

what is the direction of a ssDNA

A

5’ to 3’

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5
Q

what end of a growing strand of DNA are the free bases added to

A

3’ end
(added to 3’ end so moving away from 5’ end)

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6
Q

how does the free nucleotide attach to the strand of DNA

A

2 of the phosphate molecules get cleavered off and the remaining one is free to bond with the OH group on the Carbon 3 to form a phosphodiester bond.

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7
Q

what are the similarities (2) and differences (2) between DNA replication and transcription

A
  • they both require a template strand
  • they both work in a 5’ to 3’ direction
    differences
  • transcription has RNA polymerase whereas DNA replication has DNA polymerase
  • DNA replication requires a primer whereas transcription does not need a primer
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8
Q

what is the difference between the coding sequences of DNA in prokaryotic and eukaryotic cells

A

in prokaryotic the whole section is coding
whereas Eukaryotic cells it has section of coding (Exons) and non coding (Introns)

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9
Q

what processing to the RNA molecule must be done before it moves into the cytoplasm

A

it must have a 5’ cap put on the 5’ end and a poly A tail on the 3’ end and have the introns spliced out

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10
Q

what are the 3 steps of PCR and the temps they occur at

A

Denaturing: 95˚
Annealing: 50 - 75˚
Extension: 72˚

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11
Q

what 5 things are needed for a PCR

A
  • DNA polymerase
  • template strand
    -primer
  • dNTPs
  • Mg2+
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12
Q

what does VNTR stand for and what does it mean

A

Variable Number Tandem Repeats / Microsatellites

where a short sequence of DNA is repeated (with a variable length)

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13
Q

what is a potential problem using prokaryotic cells to make a eukaryotic product and how can we solve it

A
  • prokaryotic cells dont have introns and so cant remove it from our DNA
  • a solution would be making complementary DNA from a mRNA strand that already has it removed
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14
Q

what 2 types of dye are required in a gel electrophoresis

A
  • a dye to track the progression of the separation
  • a dye to track the sample of interest
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15
Q

what 2 types of gel are used for gel electrophoresis and when are they generally used

A

Agarose gel for larger molecules
and polyacrylamide gel for smaller molecules

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16
Q

what is isoelectric focussing

A

it is used to separate proteins based of off pH - proteins migrate to their PI ( proteins net charge at pI is 0)