Biochem - molecular Flashcards

1
Q

Charge of DNA and histones

A

negatively charged DNA (bases are negative)

positively charged histone (rich in lysine/arginine)

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2
Q

darker DNA on electron microscopy

A

heterochromatin, sterically inaccessible

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3
Q

Location of DNA methylation

A

Cytosine and adenine (to signal replicated strand)

CpG island (to repress transcription, methylation makes mute)

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4
Q

Purines vs. pyrimidines

A

purines = 2 rings (A, G)

pyrimidines = 1 ring (C, T, U)
deamination of cytosine makes uracil (which replaces thymine)

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5
Q

Increased melting temperature of DNA

A

incr. C-G content (3 H bonds!)

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6
Q

De novo purine synthesis

A

Glycine, Aspartate, Glutamine

sugar plus phosphate

then add base

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7
Q

Purine synthesis inhibitors

A

6-MP

Mycophenolate, ribavirin

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8
Q

Pyrimidine synthesis inhibitors

A

Leflunomide

Hydroxyurea (anti polycythemia)

5-FU

Methotrexate, trimethoprim (DHF reductase)

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9
Q

Purine salvage deficiencies

A

Adenosine deaminase def. - excess ATP/dATP, decr. DNA and decr. lymphos (cause of SCID!)

Lesch-Nyan = absent HGPRT (hyperuricemia, gout, pissed off, retardation, dystonia)

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10
Q

Prevents strands from reannealing

A

Single Strand Binding Proteins

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11
Q

Proofreads each added nucleotide

Elongates leading strand to the 3’ end

A

DNA polymerase III

5’ to 3’ synthesis
proofreads with 3’ to 5’ exonuclease

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12
Q

Degrades RNA primer, replaces with DNA

A

DNA polymerase I

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13
Q

Catalyzes the formation of a phosphodiester bond within a strand of double-stranded DNA
ie. Joins Okazaki fragments

A

DNA ligase

Seals the strand

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14
Q

Specific endonucleases release the oligonucleotides containing damaged bases

Gap is filled by DNA pol, sealed by ligase

A

nucleotide excision repair, occurs in G1

defective in xeroderma pigmentosum

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15
Q

Newly synthesized strand is recognized, mismatched nucleotides removed and gap is filled and resealed

A

DNA mismatch repair

defective in HNPCC

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16
Q

2 DNA fragments are brought together to repair dsDNA breaks

A

nonhomologous end joining

mutated in ataxia-telengiectasia, Fanconi anemia

17
Q

Order of RNA polymerase

A

1: rRNA (rampant)
2: mRNA (massive) - inhibited by death cap mushrooms (hepatotoxicity)
3: tRNA (tiny)

18
Q

Location of mRNA quality control

A

cytoplasmic P bodies

contain exonucleases, decapping enzymes, microRNAs

also can store mRNA for future translation

19
Q

tRNA structure

A

amino acid is bound to 3’ end (CCA)

T-arm: binds to ribosome
D-arm: recognized by aminoacyl tRNA synthetase

anti-codon loop: binds codon of mRNA

20
Q

mischarged tRNA

A

reads the usual codon but inserts the wrong amino acid

represents a mistake by aminoacyl-tRNA synthetase proofreading function

21
Q

ATP vs. GTP in the protein synthesis process

A
ATP = tRNA activation
GTP = tRNA gripping (to 40S subunit) and going places (translocation)
22
Q

Sites for elongation on ribosome

A

A site: incoming aminoacyl-tRNA
P site: accomodates growing peptide
E site: holds empty tRNA as it exits