All mutations are changes in the DNA of a gene.
Mutations in gametes are passed on to the offspring, but mutations in somatic cells affect only the individual cell. But mutations in both cells cause changes in DNA.
Types of Mutations
- Gene Rearrangements- change in a gene's position
- Gene Alterations- changes in the genetic code
- Transposons- mobile segments of DNA and they move randomly along chromosomes can cause both gene rearrangements and gene alterations
- Gene Rearrangement- in a new position a gene does not have the same regulatory control and cannot be turned on and off as efficiently or at all
- Point Mutations- a single nucleotide change
- Gene Alteration- change in the genetic code usually causes a change in the amino acid sequence
- Substitution- a different nucleotide takes the place of the original nucleotide
The possible results of substitution:
- a single amino acid is changed which can affect protein folding (shape) & function
- no change is made and the protein functions normally
- creation of an early stop codon shortens proteins
Frameshift
- changes the total number of nucleotides in a gene
- alters the reading frame, so codons are shifted & read in different triplet groups
Possible results of frameshift:
- the amino acid sequence from the point of the mutation on is different resulting in a dysfunctional protein
- stop codons may be found early
Types of Frameshift Mutations
- Insertion- a sizable length of DNA is inserted into a gene
- Deletion- segments of a gene are lost (often during meiosis)
Inversion- a section of DNA that has a reverse base order
Translocation- a section of a chromosome breaks off & attaches to a non-homologous chromosome (often during meiosis) is reciprocal hapens to both new DNA is under the inflence of different promoters- changes gene function, may break in part, so the gene cannot function