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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...

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Autores principales: Wan, Xuehua, Saito, Jennifer A., Hou, Shaobin, Geib, Scott M., Yuryev, Anton, Higa, Lynne M., Womersley, Christopher Z., Alam, Maqsudul
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
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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.
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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
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