Cargando…
Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish
Small populations with limited range are often threatened by inbreeding and reduced genetic diversity, which can reduce fitness and exacerbate population decline. One of the most extreme natural examples is the Devils Hole pupfish (Cyprinodon diabolis), an iconic and critically endangered species wi...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627712/ https://www.ncbi.nlm.nih.gov/pubmed/36321496 http://dx.doi.org/10.1098/rspb.2022.1561 |
_version_ | 1784823028941586432 |
---|---|
author | Tian, David Patton, Austin H. Turner, Bruce J. Martin, Christopher H. |
author_facet | Tian, David Patton, Austin H. Turner, Bruce J. Martin, Christopher H. |
author_sort | Tian, David |
collection | PubMed |
description | Small populations with limited range are often threatened by inbreeding and reduced genetic diversity, which can reduce fitness and exacerbate population decline. One of the most extreme natural examples is the Devils Hole pupfish (Cyprinodon diabolis), an iconic and critically endangered species with the smallest known range of any vertebrate. This species has experienced severe declines in population size over the last 30 years and suffered major bottlenecks in 2007 and 2013, when the population shrunk to 38 and 35 individuals, respectively. Here, we analysed 30 resequenced genomes of desert pupfishes from Death Valley, Ash Meadows and surrounding areas to examine the genomic consequences of small population size. We found extremely high levels of inbreeding (F(ROH) = 0.34–0.81) and an increased amount of potentially deleterious genetic variation in the Devils Hole pupfish as compared to other species, including unique, fixed loss-of-function alleles and deletions in genes associated with sperm motility and hypoxia. Additionally, we successfully resequenced a formalin-fixed museum specimen from 1980 and found that the population was already highly inbred prior to recent known bottlenecks. We thus document severe inbreeding and increased mutation load in the Devils Hole pupfish and identify candidate deleterious variants to inform management of this conservation icon. |
format | Online Article Text |
id | pubmed-9627712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96277122022-11-14 Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish Tian, David Patton, Austin H. Turner, Bruce J. Martin, Christopher H. Proc Biol Sci Genetics and Genomics Small populations with limited range are often threatened by inbreeding and reduced genetic diversity, which can reduce fitness and exacerbate population decline. One of the most extreme natural examples is the Devils Hole pupfish (Cyprinodon diabolis), an iconic and critically endangered species with the smallest known range of any vertebrate. This species has experienced severe declines in population size over the last 30 years and suffered major bottlenecks in 2007 and 2013, when the population shrunk to 38 and 35 individuals, respectively. Here, we analysed 30 resequenced genomes of desert pupfishes from Death Valley, Ash Meadows and surrounding areas to examine the genomic consequences of small population size. We found extremely high levels of inbreeding (F(ROH) = 0.34–0.81) and an increased amount of potentially deleterious genetic variation in the Devils Hole pupfish as compared to other species, including unique, fixed loss-of-function alleles and deletions in genes associated with sperm motility and hypoxia. Additionally, we successfully resequenced a formalin-fixed museum specimen from 1980 and found that the population was already highly inbred prior to recent known bottlenecks. We thus document severe inbreeding and increased mutation load in the Devils Hole pupfish and identify candidate deleterious variants to inform management of this conservation icon. The Royal Society 2022-11-09 2022-11-02 /pmc/articles/PMC9627712/ /pubmed/36321496 http://dx.doi.org/10.1098/rspb.2022.1561 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Genetics and Genomics Tian, David Patton, Austin H. Turner, Bruce J. Martin, Christopher H. Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish |
title | Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish |
title_full | Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish |
title_fullStr | Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish |
title_full_unstemmed | Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish |
title_short | Severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered Devils Hole pupfish |
title_sort | severe inbreeding, increased mutation load and gene loss-of-function in the critically endangered devils hole pupfish |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627712/ https://www.ncbi.nlm.nih.gov/pubmed/36321496 http://dx.doi.org/10.1098/rspb.2022.1561 |
work_keys_str_mv | AT tiandavid severeinbreedingincreasedmutationloadandgenelossoffunctioninthecriticallyendangereddevilsholepupfish AT pattonaustinh severeinbreedingincreasedmutationloadandgenelossoffunctioninthecriticallyendangereddevilsholepupfish AT turnerbrucej severeinbreedingincreasedmutationloadandgenelossoffunctioninthecriticallyendangereddevilsholepupfish AT martinchristopherh severeinbreedingincreasedmutationloadandgenelossoffunctioninthecriticallyendangereddevilsholepupfish |