A change in the nucleotide sequence of DNA that is heritable
People like some of the phenotypes
produced by mutant alleles
Recessive Mutations
Phenotype is associated
with the homozygous
condition
Often involve the loss of gene function
Null / Amorphic Alleles
A nonfunctional
protein is produced
OR no protein is
produced
Hypomorphic Alleles
A poorly functioning protein is produced OR reduced
amounts of a normally functioning protein is produced
Dominant Mutations
Only need one copy of allele to
see phenotype
Often involve gain/change of gene function
Dominant Hypermorphic Alleles
Negative phenotypic consequences due to the
over-production of a normal protein OR negative phenotypic
consequences due to the production of a protein with
increased activity levels
Neomorphic Alleles
Negative phenotypic consequences
due to the presence of an altered
protein that has a new function
Silent Mutation:
DNA change
results in a new
mRNA codon
that specifies
the same amino
acid
Missense Mutation:
DNA change results
in a new mRNA
codon that specifies
a different amino
acid
Nonsense Mutation: DNA change
results in a new mRNA codon that is
a STOP codon
Frameshift Mutation: DNA change
that results in a change in the reading
frame. Downstream from the
insertion/deletion, the reading frame is
shifted, which results in a very
different amino acid sequence for the
latter part of the protein
Sources of Mutations
Spontaneous: Changes in the
nucleotide sequence as a result of
errors in the DNA replication
Induced: Changes in the
nucleotide sequence which result
from exposure to radiation and
mutagenic chemicals