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PMID: 9461401 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Codon bias evolution in Drosophila. Population genetics of mutation-selection drift.

Gene ·Vol. 205 ·No. 1-2 ·1997-12-31 ·Pages 269-78

Akashi H

Abstract

Although non-random patterns of synonymous codon usage are a prominent feature in the genomes of many organisms, the relatives roles of mutational biases and natural selection in maintaining codon bias remain a contentious issue. In some species, patterns of codon bias and empirical findings on the biology of translation suggest 'major codon preference', a balance among mutation pressure, genetic drift, and weak selection in favor of translationally superior codons. Population genetics theory makes testable predictions to distinguish such a model from a strictly mutational model of codon bias. Major codon preference predicts two fitness classes of synonymous DNA changes: 'preferred' mutations from non-major to major codons and 'unpreferred' changes in the opposite direction. An extension of current statistical methods is employed to reveal differences in the within and between species dynamics of preferred and unpreferred silent mutations in Drosophila simulans. In this lineage, codon bias appears to be maintained under roughly equal magnitudes of natural selection and genetic drift. In the sibling species, D. melanogaster, however, a reduction in N(e)s, the product of effective population size and selection coefficient, appears to have allowed a genome-wide reduction in codon bias.

MeSH Terms
Animals Codon Drosophila/genetics Evolution, Molecular Gene Frequency Mutation Selection, Genetic
Chemicals
Codon
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Akashi H
Section of Evolution and Ecology, University of California, Davis 95616, USA. [email protected]
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1997-12-31
Pages
269-78
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
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