Cargando…
The Aphelenchus avenae genome highlights evolutionary adaptation to desiccation
Some organisms can withstand complete body water loss (losing up to 99% of body water) and stay in ametabolic state for decades until rehydration, which is known as anhydrobiosis. Few multicellular eukaryotes on their adult stage can withstand life without water. We still have an incomplete understa...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553787/ https://www.ncbi.nlm.nih.gov/pubmed/34711923 http://dx.doi.org/10.1038/s42003-021-02778-8 |
_version_ | 1784591652462002176 |
---|---|
author | Wan, Xuehua Saito, Jennifer A. Hou, Shaobin Geib, Scott M. Yuryev, Anton Higa, Lynne M. Womersley, Christopher Z. Alam, Maqsudul |
author_facet | Wan, Xuehua Saito, Jennifer A. Hou, Shaobin Geib, Scott M. Yuryev, Anton Higa, Lynne M. Womersley, Christopher Z. Alam, Maqsudul |
author_sort | Wan, Xuehua |
collection | PubMed |
description | Some organisms can withstand complete body water loss (losing up to 99% of body water) and stay in ametabolic state for decades until rehydration, which is known as anhydrobiosis. Few multicellular eukaryotes on their adult stage can withstand life without water. We still have an incomplete understanding of the mechanism for metazoan survival of anhydrobiosis. Here we report the 255-Mb genome of Aphelenchus avenae, which can endure relative zero humidity for years. Gene duplications arose genome-wide and contributed to the expansion and diversification of 763 kinases, which represents the second largest metazoan kinome to date. Transcriptome analyses of ametabolic state of A. avenae indicate the elevation of ATP level for global recycling of macromolecules and enhancement of autophagy in the early stage of anhydrobiosis. We catalogue 74 species-specific intrinsically disordered proteins, which may facilitate A. avenae to survive through desiccation stress. Our findings refine a molecular basis evolving for survival in extreme water loss and open the way for discovering new anti-desiccation strategies. |
format | Online Article Text |
id | pubmed-8553787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85537872021-10-29 The Aphelenchus avenae genome highlights evolutionary adaptation to desiccation Wan, Xuehua Saito, Jennifer A. Hou, Shaobin Geib, Scott M. Yuryev, Anton Higa, Lynne M. Womersley, Christopher Z. Alam, Maqsudul Commun Biol Article Some organisms can withstand complete body water loss (losing up to 99% of body water) and stay in ametabolic state for decades until rehydration, which is known as anhydrobiosis. Few multicellular eukaryotes on their adult stage can withstand life without water. We still have an incomplete understanding of the mechanism for metazoan survival of anhydrobiosis. Here we report the 255-Mb genome of Aphelenchus avenae, which can endure relative zero humidity for years. Gene duplications arose genome-wide and contributed to the expansion and diversification of 763 kinases, which represents the second largest metazoan kinome to date. Transcriptome analyses of ametabolic state of A. avenae indicate the elevation of ATP level for global recycling of macromolecules and enhancement of autophagy in the early stage of anhydrobiosis. We catalogue 74 species-specific intrinsically disordered proteins, which may facilitate A. avenae to survive through desiccation stress. Our findings refine a molecular basis evolving for survival in extreme water loss and open the way for discovering new anti-desiccation strategies. Nature Publishing Group UK 2021-10-28 /pmc/articles/PMC8553787/ /pubmed/34711923 http://dx.doi.org/10.1038/s42003-021-02778-8 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wan, Xuehua Saito, Jennifer A. Hou, Shaobin Geib, Scott M. Yuryev, Anton Higa, Lynne M. Womersley, Christopher Z. Alam, Maqsudul The Aphelenchus avenae genome highlights evolutionary adaptation to desiccation |
title | The Aphelenchus avenae genome highlights evolutionary adaptation to desiccation |
title_full | The Aphelenchus avenae genome highlights evolutionary adaptation to desiccation |
title_fullStr | The Aphelenchus avenae genome highlights evolutionary adaptation to desiccation |
title_full_unstemmed | The Aphelenchus avenae genome highlights evolutionary adaptation to desiccation |
title_short | The Aphelenchus avenae genome highlights evolutionary adaptation to desiccation |
title_sort | aphelenchus avenae genome highlights evolutionary adaptation to desiccation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553787/ https://www.ncbi.nlm.nih.gov/pubmed/34711923 http://dx.doi.org/10.1038/s42003-021-02778-8 |
work_keys_str_mv | AT wanxuehua theaphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT saitojennifera theaphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT houshaobin theaphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT geibscottm theaphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT yuryevanton theaphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT higalynnem theaphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT womersleychristopherz theaphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT alammaqsudul theaphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT wanxuehua aphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT saitojennifera aphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT houshaobin aphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT geibscottm aphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT yuryevanton aphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT higalynnem aphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT womersleychristopherz aphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation AT alammaqsudul aphelenchusavenaegenomehighlightsevolutionaryadaptationtodesiccation |