Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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
_version_ 1783472546818031616
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
work_keys_str_mv AT weinsteindeborahj thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT allensarahe thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT laumaggiecy thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT erasmusmariana thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT asalonekathrync thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT walterscontekathryn thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT deikusgintaras thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT sebrarobert thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT borgoniegaetan thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT vanheerdenesta thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT onstotttullisc thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT brachtjohnr thegenomeofasubterrestrialnematoderevealsadaptationstoheat
AT weinsteindeborahj genomeofasubterrestrialnematoderevealsadaptationstoheat
AT allensarahe genomeofasubterrestrialnematoderevealsadaptationstoheat
AT laumaggiecy genomeofasubterrestrialnematoderevealsadaptationstoheat
AT erasmusmariana genomeofasubterrestrialnematoderevealsadaptationstoheat
AT asalonekathrync genomeofasubterrestrialnematoderevealsadaptationstoheat
AT walterscontekathryn genomeofasubterrestrialnematoderevealsadaptationstoheat
AT deikusgintaras genomeofasubterrestrialnematoderevealsadaptationstoheat
AT sebrarobert genomeofasubterrestrialnematoderevealsadaptationstoheat
AT borgoniegaetan genomeofasubterrestrialnematoderevealsadaptationstoheat
AT vanheerdenesta genomeofasubterrestrialnematoderevealsadaptationstoheat
AT onstotttullisc genomeofasubterrestrialnematoderevealsadaptationstoheat
AT brachtjohnr genomeofasubterrestrialnematoderevealsadaptationstoheat