Cargando…

Strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression

Human‐driven habitat fragmentation and loss have led to a proliferation of small and isolated plant and animal populations with high risk of extinction. One of the main threats to extinction in these populations is inbreeding depression, which is primarily caused by recessive deleterious mutations b...

Descripción completa

Detalles Bibliográficos
Autores principales: Kyriazis, Christopher C., Wayne, Robert K., Lohmueller, Kirk E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857301/
https://www.ncbi.nlm.nih.gov/pubmed/33552534
http://dx.doi.org/10.1002/evl3.209
_version_ 1783646420516995072
author Kyriazis, Christopher C.
Wayne, Robert K.
Lohmueller, Kirk E.
author_facet Kyriazis, Christopher C.
Wayne, Robert K.
Lohmueller, Kirk E.
author_sort Kyriazis, Christopher C.
collection PubMed
description Human‐driven habitat fragmentation and loss have led to a proliferation of small and isolated plant and animal populations with high risk of extinction. One of the main threats to extinction in these populations is inbreeding depression, which is primarily caused by recessive deleterious mutations becoming homozygous due to inbreeding. The typical approach for managing these populations is to maintain high genetic diversity, increasingly by translocating individuals from large populations to initiate a “genetic rescue.” However, the limitations of this approach have recently been highlighted by the demise of the gray wolf population on Isle Royale, which declined to the brink of extinction soon after the arrival of a migrant from the large mainland wolf population. Here, we use a novel population genetic simulation framework to investigate the role of genetic diversity, deleterious variation, and demographic history in mediating extinction risk due to inbreeding depression in small populations. We show that, under realistic models of dominance, large populations harbor high levels of recessive strongly deleterious variation due to these mutations being hidden from selection in the heterozygous state. As a result, when large populations contract, they experience a substantially elevated risk of extinction after these strongly deleterious mutations are exposed by inbreeding. Moreover, we demonstrate that, although genetic rescue is broadly effective as a means to reduce extinction risk, its effectiveness can be greatly increased by drawing migrants from small or moderate‐sized source populations rather than large source populations due to smaller populations harboring lower levels of recessive strongly deleterious variation. Our findings challenge the traditional conservation paradigm that focuses on maximizing genetic diversity in small populations in favor of a view that emphasizes minimizing strongly deleterious variation. These insights have important implications for managing small and isolated populations in the increasingly fragmented landscape of the Anthropocene.
format Online
Article
Text
id pubmed-7857301
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-78573012021-02-05 Strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression Kyriazis, Christopher C. Wayne, Robert K. Lohmueller, Kirk E. Evol Lett Letters Human‐driven habitat fragmentation and loss have led to a proliferation of small and isolated plant and animal populations with high risk of extinction. One of the main threats to extinction in these populations is inbreeding depression, which is primarily caused by recessive deleterious mutations becoming homozygous due to inbreeding. The typical approach for managing these populations is to maintain high genetic diversity, increasingly by translocating individuals from large populations to initiate a “genetic rescue.” However, the limitations of this approach have recently been highlighted by the demise of the gray wolf population on Isle Royale, which declined to the brink of extinction soon after the arrival of a migrant from the large mainland wolf population. Here, we use a novel population genetic simulation framework to investigate the role of genetic diversity, deleterious variation, and demographic history in mediating extinction risk due to inbreeding depression in small populations. We show that, under realistic models of dominance, large populations harbor high levels of recessive strongly deleterious variation due to these mutations being hidden from selection in the heterozygous state. As a result, when large populations contract, they experience a substantially elevated risk of extinction after these strongly deleterious mutations are exposed by inbreeding. Moreover, we demonstrate that, although genetic rescue is broadly effective as a means to reduce extinction risk, its effectiveness can be greatly increased by drawing migrants from small or moderate‐sized source populations rather than large source populations due to smaller populations harboring lower levels of recessive strongly deleterious variation. Our findings challenge the traditional conservation paradigm that focuses on maximizing genetic diversity in small populations in favor of a view that emphasizes minimizing strongly deleterious variation. These insights have important implications for managing small and isolated populations in the increasingly fragmented landscape of the Anthropocene. John Wiley and Sons Inc. 2020-12-17 /pmc/articles/PMC7857301/ /pubmed/33552534 http://dx.doi.org/10.1002/evl3.209 Text en © 2020 The Authors. Evolution Letters published by Wiley Periodicals, LLC on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Kyriazis, Christopher C.
Wayne, Robert K.
Lohmueller, Kirk E.
Strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression
title Strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression
title_full Strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression
title_fullStr Strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression
title_full_unstemmed Strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression
title_short Strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression
title_sort strongly deleterious mutations are a primary determinant of extinction risk due to inbreeding depression
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857301/
https://www.ncbi.nlm.nih.gov/pubmed/33552534
http://dx.doi.org/10.1002/evl3.209
work_keys_str_mv AT kyriazischristopherc stronglydeleteriousmutationsareaprimarydeterminantofextinctionriskduetoinbreedingdepression
AT waynerobertk stronglydeleteriousmutationsareaprimarydeterminantofextinctionriskduetoinbreedingdepression
AT lohmuellerkirke stronglydeleteriousmutationsareaprimarydeterminantofextinctionriskduetoinbreedingdepression