cellular control key bits n bobs Flashcards

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1
Q

what determines the impact of the new amino acids that may be inserted as a result of a mutation?

A
  • the position and involvemet of the amino acid R group interactions within the protein
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2
Q

what is a point mutation?

A
  • a mutation to a single nucleotide of the DNA, eg where a nucleotide is switched for another
  • eg a substitution
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3
Q

explain the effect of the frameshift?

A
  • usually caused by insertion and deletion
  • changes the number of bases in the DNA sequences.
  • changes the way every successive codon is read after the point of mutation.
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4
Q

state and explain the 4 types of chromosomal mutations that involve changing the number or structure of whole chromosomes.

A

translocation –> part of one chromosome that breaks off attaches to another homologous chromosomes.
inversion -> part of the chromosome is reversed.
duplication -> the section of a chromosome is duplicated.
deletion –> loss of all parts of chromosome within a cell.

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5
Q

what is a chromosomal mutation?

A

a change in the structure or number of a whole chromosome.

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6
Q

give an example of a harmful mutations

A

sickle cell anaemia

- this results in the cell not containing the correct amount of O2 for respiration

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7
Q

what is a missense mutation?

A

these mutations result in the incorporation of an incorrect amino acid into the primary structure when the protein is synthesised.
- it usually causes proteins to be less efficient in their function

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8
Q

what is a conservative mutation?

A

when an amino acid change leads to an amino acid being coded for that was SIMILAR to the original (ie mutation is less severe)

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9
Q

what is a non conservative mutation?

A
  • when the new coded amino acid has different properties from the original.
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10
Q

what do mutagenic agents do?

A
  • they increase the frequency of mutations
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11
Q

what can causes mutations (ie changes tot he DNA sequences?

A
  • exposure to chemicals (ie UV, Bromine etc)
  • radio/chemotherapy.
  • DNA replication
  • chromosomal mutations of meiosis.
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