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frameshift

   Also found in: Encyclopedia, Wikipedia 0.10 sec.
frame´shift
a.1.(Genetics) of, pertaining to, or causing a type of mutation consisting of the insertion or deletion of one or more nucleotides in the nucleic acid structure of a gene, when the number of base pairs inserted or deleted is not a multiple of three. If the addition or deletion occurs in multiples of three, the unaffected nucleotides in the genome remain in the proper order ("frame") to be correctly translated into protein; in such cases of insertions or deletions not causing a frame shift, a functional though altered protein may be produced by the organism. Frameshift mutations cause more profound changes in the composition of the protein resulting from translation of the mutated gene.

frameshift  (frmshft)
Relating to a mutation that occurs when one or two nucleotides are added or deleted, with the result that every codon beyond the point of insertion or deletion is read incorrectly during translation. See more at point mutation.


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This 7-bp or 1-bp insertion causes a frameshift mutation in the pks15, resulting in an intact pks15/1 with additional codons (8).
These include frameshift mutations caused by nucleotide insertion or deletion, as well as missense, nonsense, and splice site mutations (Abramowicz et al.
colt in vitro model, a translesion synthesis enzyme (dinB encoded DNA polymerase IV) activity clearly promoted more important frameshift mutations (single-base deletions) in two thirds of the spontaneous mutants (10).
 
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