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The Agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species
Agassiz’s desert tortoise (Gopherus agassizii) is a long-lived species native to the Mojave Desert and is listed as threatened under the US Endangered Species Act. To aid conservation efforts for preserving the genetic diversity of this species, we generated a whole genome reference sequence with an...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451010/ https://www.ncbi.nlm.nih.gov/pubmed/28562605 http://dx.doi.org/10.1371/journal.pone.0177708 |
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author | Tollis, Marc DeNardo, Dale F. Cornelius, John A. Dolby, Greer A. Edwards, Taylor Henen, Brian T. Karl, Alice E. Murphy, Robert W. Kusumi, Kenro |
author_facet | Tollis, Marc DeNardo, Dale F. Cornelius, John A. Dolby, Greer A. Edwards, Taylor Henen, Brian T. Karl, Alice E. Murphy, Robert W. Kusumi, Kenro |
author_sort | Tollis, Marc |
collection | PubMed |
description | Agassiz’s desert tortoise (Gopherus agassizii) is a long-lived species native to the Mojave Desert and is listed as threatened under the US Endangered Species Act. To aid conservation efforts for preserving the genetic diversity of this species, we generated a whole genome reference sequence with an annotation based on deep transcriptome sequences of adult skeletal muscle, lung, brain, and blood. The draft genome assembly for G. agassizii has a scaffold N50 length of 252 kbp and a total length of 2.4 Gbp. Genome annotation reveals 20,172 protein-coding genes in the G. agassizii assembly, and that gene structure is more similar to chicken than other turtles. We provide a series of comparative analyses demonstrating (1) that turtles are among the slowest-evolving genome-enabled reptiles, (2) amino acid changes in genes controlling desert tortoise traits such as shell development, longevity and osmoregulation, and (3) fixed variants across the Gopherus species complex in genes related to desert adaptations, including circadian rhythm and innate immune response. This G. agassizii genome reference and annotation is the first such resource for any tortoise, and will serve as a foundation for future analysis of the genetic basis of adaptations to the desert environment, allow for investigation into genomic factors affecting tortoise health, disease and longevity, and serve as a valuable resource for additional studies in this species complex. |
format | Online Article Text |
id | pubmed-5451010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54510102017-06-12 The Agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species Tollis, Marc DeNardo, Dale F. Cornelius, John A. Dolby, Greer A. Edwards, Taylor Henen, Brian T. Karl, Alice E. Murphy, Robert W. Kusumi, Kenro PLoS One Research Article Agassiz’s desert tortoise (Gopherus agassizii) is a long-lived species native to the Mojave Desert and is listed as threatened under the US Endangered Species Act. To aid conservation efforts for preserving the genetic diversity of this species, we generated a whole genome reference sequence with an annotation based on deep transcriptome sequences of adult skeletal muscle, lung, brain, and blood. The draft genome assembly for G. agassizii has a scaffold N50 length of 252 kbp and a total length of 2.4 Gbp. Genome annotation reveals 20,172 protein-coding genes in the G. agassizii assembly, and that gene structure is more similar to chicken than other turtles. We provide a series of comparative analyses demonstrating (1) that turtles are among the slowest-evolving genome-enabled reptiles, (2) amino acid changes in genes controlling desert tortoise traits such as shell development, longevity and osmoregulation, and (3) fixed variants across the Gopherus species complex in genes related to desert adaptations, including circadian rhythm and innate immune response. This G. agassizii genome reference and annotation is the first such resource for any tortoise, and will serve as a foundation for future analysis of the genetic basis of adaptations to the desert environment, allow for investigation into genomic factors affecting tortoise health, disease and longevity, and serve as a valuable resource for additional studies in this species complex. Public Library of Science 2017-05-31 /pmc/articles/PMC5451010/ /pubmed/28562605 http://dx.doi.org/10.1371/journal.pone.0177708 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Tollis, Marc DeNardo, Dale F. Cornelius, John A. Dolby, Greer A. Edwards, Taylor Henen, Brian T. Karl, Alice E. Murphy, Robert W. Kusumi, Kenro The Agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species |
title | The Agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species |
title_full | The Agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species |
title_fullStr | The Agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species |
title_full_unstemmed | The Agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species |
title_short | The Agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species |
title_sort | agassiz’s desert tortoise genome provides a resource for the conservation of a threatened species |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451010/ https://www.ncbi.nlm.nih.gov/pubmed/28562605 http://dx.doi.org/10.1371/journal.pone.0177708 |
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