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frameshift

   Also found in: Encyclopedia, Wikipedia 0.01 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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Most of these studies used different strains of Salmonella typhimurium to show that DEP can induce frameshift mutations and base substitutions, presumably suggesting that DEP have a high tumorigenic potency (DeMarini et al.
Thus, in contrast to sickle cell disease where there is a single point mutation in all individuals, in the case of, for example, cystic fibrosis, at least 700 are known including mis-sense, nonsense and frameshift mutations, which lead to the production of a faulty protein, faulty processing, faulty regulation of the chloride channel--all of which lead to the symptoms of the disease.
This strain type contains the genes for binary toxin and has an 18-bp deletion and a frameshift mutation in tcdC hypothesized to result in deregulated expression of toxins A and B.
 
 
 
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