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PMID: 11886642 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

The X chromosome is a hot spot for sexually antagonistic fitness variation.

Proceedings. Biological sciences ·Vol. 269 ·No. 1490 ·2002-03-07 ·Pages 499-505

Gibson JR, Chippindale AK, Rice WR

Abstract

Sexually antagonistic alleles are selected discordantly between the sexes. Experimental evidence indicates that sexually antagonistic fitness variation is abundant in the genome of Drosophila melanogaster. Theory predicts that the X chromosome will be enriched with this type of variation. To test this prediction in D. melanogaster, we sampled, and cytogenetically cloned, 20 X chromosomes and compared their fitness variation to genome-wide levels. At the juvenile stage, in which gender roles are most similar, the X chromosome made no detectable contribution to genome-wide fitness variation. At the adult stage, in which gender roles diverge, the X chromosome was estimated to harbour 45% of the genome-wide fitness variation and 97% of the genome-wide sexually antagonistic variation. This genomic structure has important implications for the process of sexual selection because X-linked sexually antagonistic variation contributes to negative intersexual heritability for fitness, i.e. high-fitness males (females) produce, on average, low-fitness daughters (sons).

MeSH Terms
Alleles Animals Biological Evolution Drosophila melanogaster/genetics Genetic Linkage/genetics Genetic Variation/genetics Genotype Polymorphism, Genetic/genetics Reproduction/genetics Selection, Genetic Sex Characteristics X Chromosome/genetics
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Gibson Jonathan R
Department of Ecology, Evolution and Marine Biology, University of California at Santa Barbara, Santa Barbara, CA 93106-9610, USA.
Chippindale Adam K
Rice William R
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Article Info
Journal
Proceedings. Biological sciences
Abbr.
Proc Biol Sci
ISSN
0962-8452
Published
2002-03-07
Pages
499-505
Language
English
Region
England
NLM ID
101245157
PMCID
PMC1690921
Subset
IM
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