Recombination Flashcards

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1
Q

When does crossing over ocurr

A

between two chromosomes at prophase 1 of meiosis

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2
Q

Chiasma

A

the point where homologous chromosomes (maternal and paternal) cross over. Chiasmata is plural, multiple cross over events

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3
Q

Recombination

A

The rearrangement of genetic material, esp. by crossing over in chromosomes. Evolved as a mechanism to repair damaged DNA

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4
Q

Single stranded break

A

originally thought that one strand from each chromosome was broken. These strands are of the same polarity and so invade the other chromosome. Nicks made in sister strands. Rejoin in a process called invasion.

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5
Q

Holliday structure in single strand breaks and resolution

A

After strands invade and nicks are ligated a four branched holliday structure is formed. This can be resolved by cutting in two ways. if the two invading strands are cut the resultant is not a true recombinant. If the non invading strands are cut the result is a true recombinant

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6
Q

Heteroduplex DNA

A

one half from one parental duplex and one half from the other, with a hybrid (heteroduplex) section in between in true recombinant

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7
Q

Branch migration

A

holliday structure is dynamic and can move from the cross over point

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8
Q

2 stranded break

A

Reality is we now think this is the case. Chromosome A breaks in both strands. as these occur frequently

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9
Q

Steps in double stranded break repair. Homologous recombination

A

Double stranded break, limited degradation from 5’ end by exonuclease, RecA (bacteria) or Rad51 (humans) strand invasion, 3’ end of invading strand extended by polymerase, the displaced loop can be used as a template to extend the strand that was left by the invading strand, the invading strand joins its original partner and the ends are ligated, two holliday structures are resolved by cleaving phosphodiester bonds

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10
Q

RecA

A

Coats invading DNA to help it find its complementary sequence. All animals have homologues of RecA. Has two binding sites so can bind single strand and double strand. The search process induces stretching of the DNA duplex, which enhances sequence complimentarity recognition. 38KD protein. invasion from right to left

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11
Q

Gene conversion

A

If crossover occurs at the point of a gene, a mismatch of the DNA of the two inner chromatids happens. Mismatch excision repair occurs at heteroduplex joint and results in ratio of alleles in 3:1

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12
Q

Recombination in repeat sequences

A

In certain sequences on the same chromosome with similarity they can recombine if proofreading fails or be repaired by mismatch repair

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13
Q

Causes of mutations

A

UV, toxins, radiation, chemicals

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14
Q

Deamination

A

Cytosine to Uracil. Can be repaired (back to CG) or may be paired with an A leading to mutation

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15
Q

Depurination

A

A may be depurinated. It could be removed to give a frameshift mutation and deletion of AT pair or it could be repaired to be unchanged

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16
Q

Pyrimidine dimer

A

disruption by UV light can form pyrimidine dimers (C,T) that form a lesion in the DNA.

17
Q

Excision repair with pyrimidine dimer humans

A

In humans recognised by XP-C and 23b complex. TFIIH recruited which partially unwinds helix, XP-G and RPA bind and continue helicase. XP-F and XP-G cut the strand (exonuclease) and gap is filled by polymerase.

18
Q

Excision repair with dimer

A

UvAB complex binds and recruits UVrC (a leaves the complex), cuts the complex and UVrD and polymerase join, ends are ligated, repair complete

19
Q

Base excision repair

A

Dna glycosylase removes base but leaves deoxyribose, AP endonuclease and phosphodiesterase remove the sugar, DNA polymerase adds new base in

20
Q

Double strand break repair

A

Double stranded break. Loss of nucleotides from degradation. Ends ligate (non homologous end joining) or they are restored in a process involving homologous recombination (homologous end joining)