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The genome of a subterrestrial nematode reveals adaptations to heat
The nematode Halicephalobus mephisto was originally discovered inhabiting a deep terrestrial aquifer 1.3 km underground. H. mephisto can thrive under conditions of abiotic stress including heat and minimal oxygen, where it feeds on a community of both chemolithotrophic and heterotrophic prokaryotes...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6872716/ https://www.ncbi.nlm.nih.gov/pubmed/31754114 http://dx.doi.org/10.1038/s41467-019-13245-8 |
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author | Weinstein, Deborah J. Allen, Sarah E. Lau, Maggie C. Y. Erasmus, Mariana Asalone, Kathryn C. Walters-Conte, Kathryn Deikus, Gintaras Sebra, Robert Borgonie, Gaetan van Heerden, Esta Onstott, Tullis C. Bracht, John R. |
author_facet | Weinstein, Deborah J. Allen, Sarah E. Lau, Maggie C. Y. Erasmus, Mariana Asalone, Kathryn C. Walters-Conte, Kathryn Deikus, Gintaras Sebra, Robert Borgonie, Gaetan van Heerden, Esta Onstott, Tullis C. Bracht, John R. |
author_sort | Weinstein, Deborah J. |
collection | PubMed |
description | The nematode Halicephalobus mephisto was originally discovered inhabiting a deep terrestrial aquifer 1.3 km underground. H. mephisto can thrive under conditions of abiotic stress including heat and minimal oxygen, where it feeds on a community of both chemolithotrophic and heterotrophic prokaryotes in an unusual ecosystem isolated from the surface biosphere. Here we report the comprehensive genome and transcriptome of this organism, identifying a signature of adaptation: an expanded repertoire of 70 kilodalton heat-shock proteins (Hsp70) and avrRpt2 induced gene 1 (AIG1) proteins. The expanded Hsp70 genes are transcriptionally induced upon growth under heat stress, and we find that positive selection is detectable in several members of this family. We further show that AIG1 may have been acquired by horizontal gene transfer (HGT) from a rhizobial fungus. Over one-third of the genes of H. mephisto are novel, highlighting the divergence of this nematode from other sequenced organisms. This work sheds light on the genomic basis of heat tolerance in a complete subterrestrial eukaryotic genome. |
format | Online Article Text |
id | pubmed-6872716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68727162019-11-25 The genome of a subterrestrial nematode reveals adaptations to heat Weinstein, Deborah J. Allen, Sarah E. Lau, Maggie C. Y. Erasmus, Mariana Asalone, Kathryn C. Walters-Conte, Kathryn Deikus, Gintaras Sebra, Robert Borgonie, Gaetan van Heerden, Esta Onstott, Tullis C. Bracht, John R. Nat Commun Article The nematode Halicephalobus mephisto was originally discovered inhabiting a deep terrestrial aquifer 1.3 km underground. H. mephisto can thrive under conditions of abiotic stress including heat and minimal oxygen, where it feeds on a community of both chemolithotrophic and heterotrophic prokaryotes in an unusual ecosystem isolated from the surface biosphere. Here we report the comprehensive genome and transcriptome of this organism, identifying a signature of adaptation: an expanded repertoire of 70 kilodalton heat-shock proteins (Hsp70) and avrRpt2 induced gene 1 (AIG1) proteins. The expanded Hsp70 genes are transcriptionally induced upon growth under heat stress, and we find that positive selection is detectable in several members of this family. We further show that AIG1 may have been acquired by horizontal gene transfer (HGT) from a rhizobial fungus. Over one-third of the genes of H. mephisto are novel, highlighting the divergence of this nematode from other sequenced organisms. This work sheds light on the genomic basis of heat tolerance in a complete subterrestrial eukaryotic genome. Nature Publishing Group UK 2019-11-21 /pmc/articles/PMC6872716/ /pubmed/31754114 http://dx.doi.org/10.1038/s41467-019-13245-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Weinstein, Deborah J. Allen, Sarah E. Lau, Maggie C. Y. Erasmus, Mariana Asalone, Kathryn C. Walters-Conte, Kathryn Deikus, Gintaras Sebra, Robert Borgonie, Gaetan van Heerden, Esta Onstott, Tullis C. Bracht, John R. The genome of a subterrestrial nematode reveals adaptations to heat |
title | The genome of a subterrestrial nematode reveals adaptations to heat |
title_full | The genome of a subterrestrial nematode reveals adaptations to heat |
title_fullStr | The genome of a subterrestrial nematode reveals adaptations to heat |
title_full_unstemmed | The genome of a subterrestrial nematode reveals adaptations to heat |
title_short | The genome of a subterrestrial nematode reveals adaptations to heat |
title_sort | genome of a subterrestrial nematode reveals adaptations to heat |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6872716/ https://www.ncbi.nlm.nih.gov/pubmed/31754114 http://dx.doi.org/10.1038/s41467-019-13245-8 |
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