Lecture 7 The 3R Flashcards

1
Q

DNA needs be kept … and needs to be …

A

conserved, in order to keep the information that makes up the organism

flexible, in order to allow changes to accommodate in the environment of the cell

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2
Q

DNA replication

A

interphase: chromosome duplication
m-phase: mitosis and cell division
mitotic spindle

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3
Q

the Meselson-Stahl experiment

A

semi-conservative vs conservative vs dispersive

n15 and n14, replication, percentage

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4
Q

DNA synthesis

A

template strand, primer strand
5’ -> 3’ direction (free OH-group in the 3’ end)
DNA polymerase
two phosphates released

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5
Q

replication fork

A
structure formed when the helix is opened up for replication
leading strand vs lagging strand
RNA primers by DNA primase
okizaki fragments by DNA polymerase 
RNA primers erased
DNA ligase seal
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6
Q

how to open the helix

A

DNA helicase, ring structure

ATP -> ADP + P

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7
Q

how to stabilize the helix

A

single-strand DNA binding proteins (SSB)

hinder secondary structures to occur, bind the backbone of the DNA, bases still exposed to the enzymes

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8
Q

loading of the machinery

A

sliding camp

clamp loader

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9
Q

active replication fork

A

p

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10
Q

the winding problem

A

a lot of torsional stress will build if the DNA cannot rapidly rotate
solution: topoisomerase I makes a cut (nick) permitting the helix to spin. When relaxed the enzyme reconnects the broken strands

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11
Q

separating two replicated circles

A

topoisomerase II cleave and reconstruct

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12
Q

fidelity of DNA replication

A

quite high fidelity, active mechanisms to correct mistakes

DNA polymerase does the first check

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13
Q

spontaneous DNA damage/mutations

A

hydrolysis
oxidation
methylation

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14
Q

depurination and deamination

A

depurination: loss of purine base (G, A)

deamintation: loss of amino group
C -> U and therefore G -> A

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15
Q

thymine dimers

A

dangerous mutation caused by UV-light, chemical bonds between thymines formed -> not able to properly base pair with the bases introduced during the replication

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16
Q

Strand-directed Mismatch Repair System

A

MSR patrolling
MutS binds specifically to mismatches
MutL scans the DNA and detects nicks, degrades the newly made strand from the nick back to the mismatch

17
Q

Problems with DNA Repair lead to disease

A

eg Werner syndrome, xeroderma pigmentosum

18
Q

base excision repair

A

excise single bases (eg deaminated C), reconstruct

19
Q

base excision repair

A

excise sequences of DNA (eg pyramidine dymers), reconstruct