Comp Exam-Ford Flashcards

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1
Q

replication:

template:

monomer:

enzymes:

polymer:

A

DNA

dNTPs

DNA Polymerase alpha, delta, epsilon

DNA

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2
Q

transcription:

template:

monomer

enzymes:

polymer:

A

DNA

NTPs

DNA Polymerase I, II, III

RNA

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3
Q

translation:

template:

monomer:

enzyme:

polymer:

A

RNA

amino acids

ribosome

protein

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4
Q

replication:

  • initiation
  • elongation
  • termination
A
  • origin licensing/firing; ORC, MCM complex → CMG helicase, DNA polymerase epsilon
  • primase, RPC, PCNA, RPA, DNA Pol a/d/e, FEN1, Topo I, FACT, ASF1/CAF1
  • FEN1, Topo II, telomerase
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5
Q

transcription:

  • initiation
  • elongation
  • termination
A
  • TFIID/B/F/E/H, FACT, mediator (scaffold), activator, RNA Pol I, II, III, promoter-proximal pause, NELF, DSIF, P-TEFb
  • RNA Pol I, II, III; tpopisomerase; processing: PARP, CBC; spliceosome, PABP
  • Torpedo vs allosteric model
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6
Q

translation:

  • initiation
  • elongation
  • termination
A
  • eIF1/2/3/4F; ribosome; tRNA-met
  • ribosome; eEF1A/1B/2; aminoacyl-tRNAs
  • eRF1/3
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7
Q

5 features of the genetic code:

  1. ____ : no breaks within or between codons; colinear sequence from DNA → protein
  2. ____ : 1 amino acid per codon
  3. ____ : more than 1 codon per amino acid
  4. ____ : codons do not share nucleotides
  5. ____ : (almost) all life uses same code
A
  1. continuous
  2. unambiguous
  3. degenerate
  4. nonoverlapping
  5. universal
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8
Q

problems and solutions with eukaryotes:

  1. size/complexity of genome →
  2. linear genome →
  3. compartmentalization →
A
  1. histone; multiple origins of replication; introns; other RNA processing
  2. telomeres
  3. protein sorting
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9
Q

4 features of genetic material and how DNA fits these features:

  1. ____ of self :
  2. ____ of information :
  3. ____ of information :
  4. variation through ____ :
A
  1. replication: self-templating
  2. storage : repair mechanisms available
  3. expression : gene expression
  4. mutation : gene duplication
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10
Q

crossing over in meiosis, what DNA recombination mechanism is used

how does this process contribute to evolution

A

homologous recombination

gene duplication potential

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11
Q

Base excision repair:

  1. damage repaired:
  2. DNA removed:
  3. Polymerase used:
  4. other enzymes:
  5. accuracy:
A
  1. modified bases
  2. 1 nt
  3. beta or lambda
  4. glycosylase; AP endonuclease; DNA ligase
  5. high
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12
Q

nucleotide excision repair:

  1. damage repaired:
  2. DNA removed:
  3. Polymerase used:
  4. other enzymes:
  5. accuracy:
A
  • covalent adducts
  • 10-30 nt
  • epsilon or delta/kappa
  • UVR enzymes; TFIIH; DNA ligase
  • high
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13
Q

translesion synthesis:

  1. damage repaired:
  2. DNA removed:
  3. Polymerase used:
  4. other enzymes:
  5. accuracy:
A
  1. covalent adducts
  2. bypass
  3. Rev 1; iota; eta; zeta
  4. PCNA
  5. low
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14
Q

NHEJ:

  1. damage repaired:
  2. DNA removed:
  3. Polymerase used:
  4. other enzymes:
  5. accuracy:
A
  1. dsDNA breaks
  2. at ssDNA site
  3. TdT, mu or lambda
  4. Ku; DNA Ligase IV
  5. low
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15
Q

homologous recombination:

  1. damage repaired:
  2. DNA removed:
  3. Polymerase used:
  4. other enzymes:
  5. accuracy:
A
  1. dsDNA breaks; stalled replication forks
  2. exposed ends
  3. delta; eta; zeta
  4. RAD51; Spo11, MRN; RPA; BRCA2
  5. high-ish
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16
Q

RNA processing steps → description → function

  1. 5’ cap →
  2. 3’ PolyA tail
  3. splicing
A
  1. upside down G → resist degradation; initiate further processing; direct mRNA to cytosol; recruit eIFs
  2. long string of A’s → define end of mRNA; resist degradation; circularize mRNA; bind eIFs
  3. remove introns → retain exons; create diversity
17
Q

noncoding DNA: location → function:

  1. noncoding RNA gene:
  2. centromere
  3. origin of replication
  4. barrier/insulator
  5. enhancer
  6. promoter
  7. telomere
A
  1. euchromatin → transcribed
  2. heterochromatin → attach sister chromatid
  3. heterochromatin → replication start site
  4. het/euchromatin junction → stops heterochromatin
  5. upstream of promoter → transcription activator binding site
  6. TATA box, INR, DPE, BRE → transcription start site
  7. heterochromatin → ends of linear chromosomes (T loop)
18
Q

noncoding RNA: location → function:

  1. rRNA
  2. tRNA
  3. snRNA
  4. snoRNA
  5. miRNA
  6. siRNA
  7. piRNA
  8. lncRNA
  9. TERC
  10. introns
  11. UTRs
A
  1. nucleolus to cytosol → ribosome catalysis
  2. cytosol → carry amino acids
  3. nucleus, cajal bodies → part of spliceosome
  4. nucleolus, cajal bodies→ RNA modification
  5. cytosol → gene silencing
  6. cytosol, nucleus → gene silencing
  7. nucleus → silence transposons
  8. nucleus, cytosol → signal, decoy, guide, scaffold
  9. nucleus → telomerase template
  10. remain in nucleus → removed from mRNA
  11. part of mRNA → regulation of mRNA
19
Q

what are 2 signals that cue Nonsense Mediated Decay of mRNAs

A

retained intron

stop codon too far from 3’ UTR

20
Q

topological equivalencies:

  1. nucleus = ____
  2. secretory/endocytic pathway organelles = ____ , golgi, endosomes, lysosome
A
  1. cytosol
  2. ER