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PMID: 17687667 Published · ppublish English Journal Article Research Support, N.I.H., Intramural Review

Too many mutants with multiple mutations.

Critical reviews in biochemistry and molecular biology ·Vol. 42 ·No. 4 ·2007-00-00 ·Pages 247-58

Drake JW

Abstract

It has recently become clear that the classical notion of the random nature of mutation does not hold for the distribution of mutations among genes: most collections of mutants contain more isolates with two or more mutations than predicted by the mutant frequency on the assumption of a random distribution of mutations. Excesses of multiples are seen in a wide range of organisms, including riboviruses, DNA viruses, prokaryotes, yeasts, and higher eukaryotic cell lines and tissues. In addition, such excesses are produced by DNA polymerases in vitro. These "multiples" appear to be generated by transient, localized hypermutation rather than by heritable mutator mutations. The components of multiples are sometimes scattered at random and sometimes display an excess of smaller distances between mutations. As yet, almost nothing is known about the mechanisms that generate multiples, but such mutations have the capacity to accelerate those evolutionary pathways that require multiple mutations where the individual mutations are neutral or deleterious. Examples that impinge on human health may include carcinogenesis and the adaptation of microbial pathogens as they move between individual hosts.

MeSH Terms
Adaptation, Biological Animals Evolution, Molecular Humans Mutagenesis/genetics Mutation/genetics Neoplasms/genetics
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Drake John W
Laboratory of Molecular Genetics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709-2233, USA. drake@niehs.nih.gov
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Article Info
Journal
Critical reviews in biochemistry and molecular biology
Abbr.
Crit Rev Biochem Mol Biol
ISSN
1040-9238
Published
2007-00-00
Pages
247-58
Language
English
Region
England
NLM ID
8903774
PMCID
PMC2265383
Subset
IM
Grants
Intramural NIH HHS · Z01 ES065016-08 · United States
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