Hostname: page-component-78c5997874-j824f Total loading time: 0 Render date: 2024-11-02T20:53:36.181Z Has data issue: false hasContentIssue false

A QTL analysis of female variation contributing to refractoriness and sperm competition in Drosophila melanogaster

Published online by Cambridge University Press:  15 December 2005

MARA K. N. LAWNICZAK
Affiliation:
Center for Population Biology, Section of Evolution and Ecology, University of California at Davis, Davis, CA 95616, USA Current address: Department of Biology, Darwin Building, University College London, London WC1E 6BT, UK. Tel: +44 (0)20 7679 4396. e-mail: [email protected]
DAVID J. BEGUN
Affiliation:
Center for Population Biology, Section of Evolution and Ecology, University of California at Davis, Davis, CA 95616, USA

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Sperm competition is an important fitness component in many animal groups. Drosophila melanogaster males exhibit substantial genetic variation for sperm competitive ability and females show considerable genetic variation for first versus second male sperm use. Currently, the forces responsible for maintaining genetic variation in sperm competition related phenotypes are receiving much attention. While several candidate genes contributing to the variation seen in male competitive ability are known, genes involved in female sperm use remain largely undiscovered. Without knowledge of the underlying genes, it will be difficult to distinguish between different models of sexual selection such as cryptic female choice and sexual conflict. We used quantitative trait locus (QTL) mapping to identify regions of the genome contributing to female propensity to use first or second male sperm, female refractoriness to re-mating, and early-life fertility. The most well supported markers influencing the phenotypes include 33F/34A (P2), 57B (refractoriness) and 23F/24A (fertility). Between 10% and 15% of the phenotypic variance observed in these recombinant inbred lines was explained by these individual QTLs. More detailed investigation of the regions detected in this experiment may lead to the identification of genes responsible for the QTLs identified here.

Type
Research Article
Copyright
© 2005 Cambridge University Press