what is a spontaneous mutation
due to natural processes such as failure in proofreading while copying DNA
what is an induced mutation
caused by external factors such as UV light, radiation, drugs or mutagens
what is a mutation
a change in the dna sequence of an organism, changes can occur in a single dna base or in larger segments of chromosomes. They can affect how proteins are made and may be harmful, beneficial or neutral
what is an inherited mutation
passed on from the parents to the offspring
what is an insertion mutation
one or more bases are added.
what is a deletion mutation
one or more bases are deleted.
what is a substitution mutation
a base gets replaced with a different base.
what is a frameshift mutation
Deletion or insertion which leads to the whole DNA strand being read incorrectly due to the frame of reading, the rest of the strand will be read incorrectly.
what is a silent mutation
the third base is less important. Therefore, when there is a change in the last base of a codon, the amino acid remains the same and don’t cause any change in the proteins.
what is a non-sense mutation
The coding of a “STOP” codon, instead of a normal amino acid. This leads to formation of shorter protein sequences is less functional
what is a mis-sense mutation
a change in amino sequence. Will cause changes
what is a neutral mutation
no selective advantage or disadvantage.
what is a point mutation
a single base changed
what is a Duplication mutation
segment of dna is copied
what is a translocation mutation
A segment of DNA moves to another chromosome. May disrupt gene function.
give an example of a beneficial mutation
coat colour in rock pocket mice
mutation changes fur colour from light to dark, these dark coloured mice are better camouflaged on volcanic rock
give an example of a harmful mutation
spider leg syndrome in sheep, a recessive gene that causes skeletal deformities such as twisted spines and long, spider like legs
give an example of a neutral mutation
Synonymous Codon Changes in Cattle, a silent mutation that causes no change in protein function or phenotype