3.8.1 - The alteration of the sequence of bases in DNA can alter the structure of proteins Flashcards
Topic 8
What is a gene mutation?
● A change in the base sequence of DNA (on chromosomes)
● Can arise spontaneously during DNA replication (interphase)
What is a mutagenic agent?
A factor that increases rate of mutation, eg. ultraviolet (UV) light or alpha particles
Explain how a gene mutation can lead to the production of
a non-functional protein or enzyme (general)
- Changes sequence of base triplets in DNA so changes sequence of codons on mRNA
- So changes sequence of amino acids in the encoded polypeptide
- So changes position of hydrogen / ionic / disulphide bonds (between amino acids)
- So changes tertiary structure (shape) of protein
- Enzymes - active site changes shape so substrate can’t bind, enzyme-substrate complex can’t form
Describe the different types of gene mutations
- Substitution
> A base / nucleotide is replaced by a different base / nucleotide in DNA - Addition
> 1 or more bases / nucleotides are added to the DNA base sequence - Deletion
> 1 or more bases / nucleotides are lost from the DNA base sequence - Duplication
> A sequence of DNA bases / nucleotides is repeated / copied - Inversion
> A sequence of bases / nucleotides detaches from the DNA sequence, then rejoins at the same position in the reverse order - Translocation
> A sequence of DNA bases / nucleotides detaches and is inserted at a different location within the same or a different chromosome
Explain why not all gene mutations affect the sequence of amino acids
● Some substitutions change only 1 triplet code / codon which could still code for the same amino acid
○ As the genetic code is degenerate (an amino acid can be coded for by more than one triplet)
● Some occur in introns which do not code for amino acids as they are removed during splicing
Explain why a change in amino acid sequence is not always harmful
● May not change tertiary structure of protein (if position of ionic / disulphide / H bonds don’t change)
● May positively change the properties of the protein, giving the organism a selective advantage
Explain what is meant by a frameshift
● Occurs when mutations (addition, deletion, duplication or translocation)
change the number of nucleotides / bases by a number not divisible by 3
● This shifts the way the genetic code is read, so all the DNA triplets / mRNA
codons downstream from the mutation change (so significant effects - Effects on the encoded polypeptide are significant)
Explain how mutations can lead to production of shorter polypeptides
● Deletion or translocation → triplet(s) / codon(s) missing so amino acid(s) missing
● Substitution, addition, deletion, duplication, inversion or translocation → premature stop triplet / codon
(doesn’t code for amino acids; terminates translation) so amino acids missing at end of polypeptide