11.05.2013 Molecular Biology 4 Flashcards

1
Q

Accurate mechanism for replication

  • repair of accidental lesion
  • -is required for genetic (instability/stability)
A

stability

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2
Q

(transition/transversions)substitution of a pyrimidine with a purine or vice versa.

A

tranversion

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3
Q

(transition/transversions)substitution of a pyrimidine with another pyrimidine or a purine with another purine.

A

transition

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4
Q

First level of repair during replication is ?

A

3’ to 5’ exonuclease activty of DNA polymerase

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5
Q

T/F Distortion in the DNA helix is recognized and repaired by strand-directed mismatch repair

A

T

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6
Q

Single strand breaks or nicks provide the repair signal.

-mechansims for recognizing mismatch in (e.coli/mammalian cells)

A

mammalian cells

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7
Q

Both strands are methylated (dam methylase) at A in the sequence GATC.
There is a lag in the methylation of GATC sequence in the newly synthesized strand
(e.coli/mammalian cells)

A

e.coli

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8
Q

(MutS/MutL) recognizes mismatched bases

A

Mut S

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9
Q

(MutS/MutL)scans the DNA
for a nick to determine
the newly replicated
DNA.

A

MutL

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10
Q

T/F Colon cancer phenotype has FAP stands for familial adenomatous polyposis and HNPCC stands for hereditary non-polyposis

A

T

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11
Q

(transversions/frameshift) due to addition/deletion of bases

A

frameshift

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12
Q
Cellular metabolic activity
Heat 
Extreme pH
Radiations
Substances in environment
--- can all case what?
A

structural alteration in DNA bases

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13
Q

(spontaneous changed/UV damage) sepurination, deamination

A

spontaneous changed

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14
Q

(spontaneous changed/UV damage) pyrimidine dimers

A

UV damage

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15
Q

(Depurination/deamination) converst C to U

A

damination

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16
Q

(Depurination/deamination) removes a purine from the nucleotide

A

depurination

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17
Q

which one of the DNA bases would not undergo deamination?

guanin/cytosine/thymine

A

thymine has no amino group

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18
Q

T/F mehtylated cytosine is commonly found in DNA

19
Q

Uv induces pyrimidne (A or G/ Cor T) dimers

20
Q

(deamination/depurination) changes the base

A

deamination

21
Q

(deamination/depurination) leads to deletion

A

depurination

22
Q

(Base excision repair/Nucleotide excision repair)Specific base is removed and repaired

A

Base excision repair

23
Q

(Base excision repair/Nucleotide excision repair)A stretch of DNA strand is removed and new strand with correct base is synthesized

A

Nucleotide excision repair

24
Q

(T/U) is an unusual base for DNA

25
(RAD3/RAD6/RAD52)excision repair
RAD 3
26
(RAD3/RAD6/RAD52) recombination-mediated repair
rad6
27
(RAD3/RAD6/RAD52) post replication repair
rad 52
28
yeast is best model system characterized for (prokaryote/eukaryotic) repari
eukaryotic
29
T/F active genese are preferentially repaired
T
30
(RAD3/RAd6) a helicase is required for repair is componenet of transcription factore associated with (DNA/RNA) polymerase
Rad3, RNA
31
recombination , ionizing radiation | -double stand breaks are(repaired/occur)
occur
32
Homologous end-joining (HEJ) Non-homologous end-joining (NHEJ) double strands breaks are (repaired/occur)
repaired
33
(nonhomologous/homologous) end-joining results in loss of original sequence
non-homologous
34
(nonhomologous/homologous) repair of double stranded breaks has no loss of sequences
homologous
35
T/F BRCA1 and BRCA2 predispose women to breast and ovarian cancer
T
36
(BRCA1/BRCA2) 1863 amino acids
BRCA1
37
(BRCA1/BRCA2) 3418 amino acids
BRCA2
38
(BRCA1/BRCA2)also involved in transcriptional regulation of genes activated in response to DNA damage.
BRCA1
39
(BRCA1/BRCA2)Initial studies indicated involvement of BRCA1 in repairing DNA damage.
BRCA1
40
BRCA1 and BRCA2 interact with other proteins that activate repair of double strand breaks and initiate (homologous/nonhomologous) recombination.
homologous
41
Werner syndrome is autosomal recessive what type of manifest in the eye does it have?
cataracts
42
``` Autosomal recessive: stunted growth sunlight sensitivity chromosome breakage immunologic deficiency infertility increased risk for neoplasia --describes (bloom syndrome/werner syndrome) ```
bloom syndrome
43
Autosomal recessive cataracts changing of skin conditions atypical short stature premature graying or thinning of the hair. Patients also often develop hypogonadism, osteoporosis, diabetes mellitus, atherosclerosis and cancers (sarcomas) --describes (bloom syndrome/werner syndrome)
werner syndrome
44
both werner syndrome and bloom syndrome mutations in the helicase of Rec Q family
T