Mutations Flashcards

1
Q

What are the 2 categories of mutations and briefly describe?

A
  • Germline: Occurs in cells that produce gametes (e.g. sperm mother cell/ stem cells) & affects offspring (inherited)
  • Somatic: Occurs in somatic cells & affect cells/tiss. of individual
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2
Q

What can are the types of mutation that can occur in a gene?

A
  • Frameshift bc of insertion/deletion of 1+ bp (usually introduce premature STOP codon)
  • Substitution: 1bp is changed to another bp during replication
  • Copy number variation
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3
Q

Differentiate b/w the 2 class of mutations (that occur in the DNA)

A
  • Gene: point mutation- change in 1 bp

- Chromosomal: (gene/)portion in chromosome changes w/in chromosome

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4
Q

Types of base substitution in point mutations & the effects

A
  • Silent mutation: △ in 3rd bp in codon ≠ △ AA
  • Missense mutation: △ 1st/2nd bp in codon = △AA (structure & function may/not △)
  • Nonsense mutation: △ in bp = STOP codon = premature termination of translation
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5
Q

Differentiate b/w transition & transversion mutations in base substitution

A
  • Transitions: △ bases w/in purines [A&G] (or pyrimidine [T&C])
  • Transverse: △ bases from purine to pyrimidine, vice versa (e.g. A -> T or C
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6
Q

Differentiate b/w the 2 types of copy number variation

A
  • Gene amplification: increase no. of genes sequ. in DNA = increase no. of proteins
  • Trinucleotide (microsatellite) repeats: 3 bases repeated many times in DNA replication = expand size of OG DNA
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7
Q

What’s the difference b/w forward & reverse mutation when referring to the effects of AA/gene sequence?

A
  • FWD: loss of wild-type (normal) allele

- RVS: Resores the WT allele (or function) e.g. 2 mutations on a same gene = may cause proper function

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8
Q

What are the phenotypic effects of mutation?

A
  • Loss of function: recessive - give total/partial loss

- Gain of function: dominant - create new trait & hyperactivation of protein

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9
Q

What are suppressor mutations & 2 types?

A

mutation that suppresses the effect of another mutation

  • Intragenic suppressor: mutations that occur @ the same gene => can restore codon sequ. = AA sequ.
  • Intergenic suppressor: mutations occur in diff. genes, but the interaction of the proteins made are normal
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10
Q

Types of chromosomal mutations & briefly describe

A
  • Deletion: a region of chromo. is lost = genes lost
  • Duplication: region is repeated = genes doubled
  • Inversion: region broken off & rejoin in reverse order
  • Translocation: a region from 1 chromo. break & attaches to another chromo.
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11
Q

What are the spontaneous replication errors?

A
  • Incorporated error: incorrect base added (wobble)
  • Strand slippage: new strand form a loop = in next new strand a base(s) is added (insertion). OR template strand loops = base(s) missed when replicated (deletion in new strand)
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12
Q

What are the spontaneous chemical errors & differentiate?

A
  • Depurination: lose purine base bc covalent bond b/w 1’C (sugar) & base breaks => no template for replication (apurinic site) = base randomly added (A)
  • Deamination: lose NH2 group from base e.g. C (-NH2) => U so in replication new strand will have A (not G)
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13
Q

Types of chemically induced mutations & causes

A
  • Base analogies: chemicals - have same structure as bases incorporated in DNA & may alter base pairing e.g. 5 bromo-uracil replaces T => pairs w/ A but sometimes G
  • Deamination
  • Add. -OH groups: hydroxylamine (NH2OH) adds hydroxyl group to C => like T = pair w/ A (not G)
  • Alkylating agents: add meth/ethyl to nucleotides e.g. G => like A = pair w/ T
  • Oxidation: free-radicals (H2O2) damage DNA e.g. G => 8-oxoguanine => pairs w/ A not G
  • Intercalating agents: chemicals inserted b/w “rungs” (bases) = distort 3D structure => insertion/deletion during replication = frameshift
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14
Q

Types of radiation induced mutations & causes

A
  • Ionising radiation: break PO bond => ds breaks in DNA

- Non-ionising radiation: bases absorb UV => form bonds w/ adjacent pyrimidine e.g. 2x T = T dimer = blocks replication

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15
Q

What are transposable elements and causes?

A

piece of DNA (insertion sequence) that can randomly insert itself in a genome
=> disrupt coding seq.
=> prevent activation of promoter
=> activate genes inappropriately

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16
Q

Describe the process of mismatch repair (in E. coli)

A
  1. After replication, A in GATC is methylated on old strand
  2. mis-match repair complexes brings unmethylated GATC (on new strand) close to mismatched base(s)
  3. nicks near unmethylated GATC and DNA in b/w mismatch base(s) & GATC is degraded
  4. DNA pol & DNA ligase fill area w/ correct base
17
Q

Describe direct repair (in O6-methylguanine & thymine dimers)

A
  • fixes damaged base rather than remove
    a) O6-methylguanine (methyltransferase remove CH3) -> guanine
    b) photolyase breaks covalent bonds in b/w thymine dimers (photo-reactivation)
18
Q

Describe the process of base excision repair

A
  1. (specific) DNA glycosylase detect modified base (e.g. U from deaminated C) & removes base @ 1’ C of sugar
  2. AP (apurinic/apyrimidinic) endonuclease cuts @ PO bond
  3. deoxyribose sugar removed
  4. DNA pol. puts correct nucleotide & DNA ligase repairs PO bonds
19
Q

Describe the process of nucleotide excision repair

A
  1. (XPC) complex of enzymes scans & encounter damaged DNA (e.g. pyrimidine dimers)
  2. endonuclease nicks a couple of bases away from damaged DNA
  3. removal of cut strand by DNA helicase
  4. resynthesis by DNA pol
  5. ligation of DNA ligase
20
Q

*Describe the difference in non-& homologous repair process of ds breaks

A
    • Homologous: uses (near) identical genetic info. from (sister chromatid) => same og DNA
    • Non-: not same as og DNA
21
Q

Describe cisplatins mechanism (as a chemotherapy drug)

A

cisplatin binds to G&G in dsDNA ≠ transcribed = (mutated) genes -> more mutated ≠ able to produce appropriate proteins for repair in cancer cell ≠ survive