Cargando…

Heterozygote Advantage for Fecundity

Heterozygote advantage, or overdominance, remains a popular and persuasive explanation for the maintenance of genetic variation in natural populations in the face of selection. However, despite being first proposed more than 80 years ago, there remain few examples that fit the criteria for heterozyg...

Descripción completa

Detalles Bibliográficos
Autores principales: Gemmell, Neil J., Slate, Jon
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1762409/
https://www.ncbi.nlm.nih.gov/pubmed/17205129
http://dx.doi.org/10.1371/journal.pone.0000125
_version_ 1782131565115998208
author Gemmell, Neil J.
Slate, Jon
author_facet Gemmell, Neil J.
Slate, Jon
author_sort Gemmell, Neil J.
collection PubMed
description Heterozygote advantage, or overdominance, remains a popular and persuasive explanation for the maintenance of genetic variation in natural populations in the face of selection. However, despite being first proposed more than 80 years ago, there remain few examples that fit the criteria for heterozygote advantage, all of which are associated with disease resistance and are maintained only in the presence of disease or other gene-by-environment interaction. Here we report five new examples of heterozygote advantage, based around polymorphisms in the BMP15 and GDF9 genes that affect female fecundity in domesticated sheep and are not reliant on disease for their maintenance. Five separate mutations in these members of the transforming growth factor β (TGFβ) superfamily give phenotypes with fitness differentials characteristic of heterozygous advantage. In each case, one copy of the mutant allele increases ovulation rate, and ultimately litter size per ewe lambing, relative to the wildtype. However, homozygous ewes inheriting mutant alleles from both parents have impaired oocyte development and maturation, which results in small undeveloped ovaries and infertility. Using data collected over many years on ovulation rates, litter size, and lambing rates, we have calculated the equilibrium solution for each of these polymorphisms using standard population genetic theory. The predicted equilibrium frequencies obtained for these mutant alleles range from 0.11 to 0.23, which are amongst the highest yet reported for a polymorphism maintained by heterozygote advantage. These are amongst the most frequent and compelling examples of heterozygote advantage yet described and the first documented examples of heterozygote advantage that are not reliant on a disease interaction for their maintenance.
format Text
id pubmed-1762409
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-17624092007-01-04 Heterozygote Advantage for Fecundity Gemmell, Neil J. Slate, Jon PLoS One Research Article Heterozygote advantage, or overdominance, remains a popular and persuasive explanation for the maintenance of genetic variation in natural populations in the face of selection. However, despite being first proposed more than 80 years ago, there remain few examples that fit the criteria for heterozygote advantage, all of which are associated with disease resistance and are maintained only in the presence of disease or other gene-by-environment interaction. Here we report five new examples of heterozygote advantage, based around polymorphisms in the BMP15 and GDF9 genes that affect female fecundity in domesticated sheep and are not reliant on disease for their maintenance. Five separate mutations in these members of the transforming growth factor β (TGFβ) superfamily give phenotypes with fitness differentials characteristic of heterozygous advantage. In each case, one copy of the mutant allele increases ovulation rate, and ultimately litter size per ewe lambing, relative to the wildtype. However, homozygous ewes inheriting mutant alleles from both parents have impaired oocyte development and maturation, which results in small undeveloped ovaries and infertility. Using data collected over many years on ovulation rates, litter size, and lambing rates, we have calculated the equilibrium solution for each of these polymorphisms using standard population genetic theory. The predicted equilibrium frequencies obtained for these mutant alleles range from 0.11 to 0.23, which are amongst the highest yet reported for a polymorphism maintained by heterozygote advantage. These are amongst the most frequent and compelling examples of heterozygote advantage yet described and the first documented examples of heterozygote advantage that are not reliant on a disease interaction for their maintenance. Public Library of Science 2006-12-27 /pmc/articles/PMC1762409/ /pubmed/17205129 http://dx.doi.org/10.1371/journal.pone.0000125 Text en Gemmell, Slate. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gemmell, Neil J.
Slate, Jon
Heterozygote Advantage for Fecundity
title Heterozygote Advantage for Fecundity
title_full Heterozygote Advantage for Fecundity
title_fullStr Heterozygote Advantage for Fecundity
title_full_unstemmed Heterozygote Advantage for Fecundity
title_short Heterozygote Advantage for Fecundity
title_sort heterozygote advantage for fecundity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1762409/
https://www.ncbi.nlm.nih.gov/pubmed/17205129
http://dx.doi.org/10.1371/journal.pone.0000125
work_keys_str_mv AT gemmellneilj heterozygoteadvantageforfecundity
AT slatejon heterozygoteadvantageforfecundity