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a level biology cellular control summary module 6

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summary of topic of cellular control in module 6, including gene expression, mutations, hox genes, mitosis and apostosis

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  • May 27, 2024
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erikakumar
GENETICS
CELLULAR CONTROL
___




MUTATION
Change in the sequence of bases in DNA

May disrupt protein synthesis

1 nucleotide : point

Caused by … of nucleotides

● Substitution: changes the codon

New codon codes for a different amino acid →change in primary structure of protein

Degenerate nature of genetic code : new codon may still code for the same amino acid leading
to no change in protein synthesised

, 2



Position & involvement of amino acid in R group interactions within protein determines
impact of new amino acid on function of protein

Eg. amino acids have role in active site = enzyme can’t act as a biological catalyst

● Deletion
● Insertion

Frameshift mutation

Triplet code (sequence of bases transcribed consecutively in non-overlapping groups of 3 =
reading frame of a sequence of bases)

Addition & deletion of nucleotide shifts reading frame = change every successive codon from
the point of mutation

N. nucleotides changed is multiple of 3 = reading frame not changed, but protein affected as
new amino acid added



Effects
No effect: normally functioning proteins still synthesised. In non-coding regions (introns) or
code for same amino acid

Damaging: phenotype affected negatively as protein not synthesised or non-functional

Beneficial: synthesised protein results in new useful characteristic in phenotype



Causes
Rate of mutation increased by mutagens (bio, physical or chemical agent)

Spontaneous depurination / depyrimidination → insertion of incorrect base through complementary
base pairing in DNA replication

Free radicals (oxidising agents) affect structures of nucleotides & disrupt base pairing

Antioxidants (anticarcinogens) negate effects of free radicals

★ Ionising radiation (eg. X-rays) break 1+ DNA strand

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