alteration of bases Flashcards
what is a mutation
an alteration to the DNA base sequence
often arise spontaneously during DNA replication
what are addition and deletion mutations
where one or more nucleotides (bases) are either inserted or deleted from the DNA sequence
what is substitution mutation
where one nucleotide (base) in the DNA sequence is replaced by another
what is a duplication mutation
where one or more nucleotides (bases) duplicate and repeat
what is an inversion mutation
where a group of nucleotides (bases) become separated from the DNA sequence, then rejoin in the reverse order
what is a translocation mutation
where a group of nucleotides (bases) become separated from the DNA sequence, and are then inserted into the DNA of a different chromosome
which mutations are most likely to have an impact
insertion, deletion, duplication and translocation
- produce a frameshift - entire amino acid sequence produced will be different
which mutations are most likely to have a smaller impact and why
substitution, inversion
- they only alter one or very few triplets
- the amino acid sequence may not be affected due to degenerate nature of the genetic code
what is a mutagenic agent
factors that increase the rate of gene mutations
chemical mutagens eg alcohol
ionising radiation eg UV