A change in the base sequence of DNA.
They can arise spontaneously during DNA replication.
When a base is removed from a DNA nucleotide sequence, a frame shift occurs. This changes all of the triplet codes after the mutation, as well as the one where the base has been removed.
When a base is substituted for another, the code will only be changed for that triplet code, no others will be affected. It may mean that there is no change in the polypeptide coded for, due to the degenerate nature of the genetic code. Or the polypeptide coded for may change by that one amino acid. In extreme cases the polypeptide may be truncated due to the presence of a new ‘stop’ triplet code.
Mutagenic agents such as ionising radiation or carcinogenic chemicals.
Chromosome mutations can arise spontaneously by chromosome non-disjunction during meiosis.
Chromosome mutations include: changes in the whole set of chromosome, such as polyploidy. Or changes in the number of individual chromosomes, when chromosomes fail to separate during meiosis.
When individual homologous pairs of chromosomes fail to separate during meiosis, so there will be more than 2 chromosomes in a homologous pair in the offspring.
A change in nucleotide sequence gene; causes a change in amino acid sequence or primary structure of the protein; Change in hydrogen / ionic / disulfide bonds; Change in the tertiary structure;
IF enzyme:
Change in active site; Substrate not complementary so no enzyme-substrate complexes form.