A single QTL with large effect is associated with female functional virginity in an asexual parasitoid wasp.

asexuality candidate genes female functional virginity introgression linkage map loss of sex resistance to mating single major QTL

Journal

Molecular ecology
ISSN: 1365-294X
Titre abrégé: Mol Ecol
Pays: England
ID NLM: 9214478

Informations de publication

Date de publication:
05 2021
Historique:
revised: 07 02 2021
received: 06 11 2020
accepted: 22 02 2021
pubmed: 28 2 2021
medline: 22 6 2021
entrez: 27 2 2021
Statut: ppublish

Résumé

During the transition from sexual to asexual reproduction, a suite of reproduction-related sexual traits become superfluous, and may be selected against if costly. Female functional virginity refers to asexual females resisting to mate or not fertilizing eggs after mating. These traits appear to be among the first that evolve during transitions from sexual to asexual reproduction. The genetic basis of female functional virginity remains elusive. Previously, we reported that female functional virginity segregates as expected for a single recessive locus in the asexual parasitoid wasp Asobara japonica. Here, we investigate the genetic basis of this trait by quantitative trait loci (QTL) mapping and candidate gene analyses. Consistent with the segregation of phenotypes, we found a single QTL of large effect, spanning over 4.23 Mb and comprising at least 131 protein-coding genes, of which 15 featured sex-biased expression in the related sexual species Asobara tabida. Two of the 15 sex-biased genes were previously identified to differ between related sexual and asexual population/species: CD151 antigen and nuclear pore complex protein Nup50. A third gene, hormone receptor 4, is involved in steroid hormone mediated mating behaviour. Overall, our results are consistent with a single locus, or a cluster of closely linked loci, underlying rapid evolution of female functional virginity in the transition to asexuality. Once this variant, causing rejection to mate, has swept through a population, the flanking region does not get smaller owing to lack of recombination in asexuals.

Identifiants

pubmed: 33638236
doi: 10.1111/mec.15863
pmc: PMC8252104
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1979-1992

Informations de copyright

© 2021 The Authors. Molecular Ecology published by John Wiley & Sons Ltd.

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Auteurs

Wen-Juan Ma (WJ)

Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, The Netherlands.
Department of Molecular Biosciences, University of Kansas, Lawrence, KS, USA.

Bart A Pannebakker (BA)

Laboratory of Genetics, Wageningen University and Research, Wageningen, The Netherlands.

Xuan Li (X)

Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, The Netherlands.

Elzemiek Geuverink (E)

Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, The Netherlands.

Seyed Yahya Anvar (SY)

Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.

Paris Veltsos (P)

Department of Ecology and Evolutionary Biology, University of Kansas, Lawrence, KS, USA.

Tanja Schwander (T)

Department of Ecology and Evolution, University of Lausanne, Lausanne, Switzerland.

Louis van de Zande (L)

Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, The Netherlands.

Leo W Beukeboom (LW)

Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, The Netherlands.

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