The alteration of the sequence of bases in DNA can alter the structure of proteins Flashcards
What is a gene mutation?
● A change in the base sequence of DNA
● 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 order 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
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
● A frameshift occurs when gene mutations (eg. addition, deletion,
duplication or translocation) change the number of nucleotides /
bases by any 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
● The sequence of amino acids encoded changes accordingly and
the effects on the encoded polypeptide are significant
If a multiple of 3 bases is added / removed there won’t be a frameshift, but extra / less triplets will result in extra /
less amino acids in the encoded polypeptide.
A frameshift could also lead to production of a stop codon (that doesn’t code for amino acids so terminates
translation), resulting in a shorter polypeptide.