Cargando…

Comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge

Anhydrobiosis represents an extreme example of tolerance adaptation to water loss, where an organism can survive in an ametabolic state until water returns. Here we report the first comparative analysis examining the genomic background of extreme desiccation tolerance, which is exclusively found in...

Descripción completa

Detalles Bibliográficos
Autores principales: Gusev, Oleg, Suetsugu, Yoshitaka, Cornette, Richard, Kawashima, Takeshi, Logacheva, Maria D., Kondrashov, Alexey S., Penin, Aleksey A., Hatanaka, Rie, Kikuta, Shingo, Shimura, Sachiko, Kanamori, Hiroyuki, Katayose, Yuichi, Matsumoto, Takashi, Shagimardanova, Elena, Alexeev, Dmitry, Govorun, Vadim, Wisecaver, Jennifer, Mikheyev, Alexander, Koyanagi, Ryo, Fujie, Manabu, Nishiyama, Tomoaki, Shigenobu, Shuji, Shibata, Tomoko F., Golygina, Veronika, Hasebe, Mitsuyasu, Okuda, Takashi, Satoh, Nori, Kikawada, Takahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175575/
https://www.ncbi.nlm.nih.gov/pubmed/25216354
http://dx.doi.org/10.1038/ncomms5784
_version_ 1782336500875132928
author Gusev, Oleg
Suetsugu, Yoshitaka
Cornette, Richard
Kawashima, Takeshi
Logacheva, Maria D.
Kondrashov, Alexey S.
Penin, Aleksey A.
Hatanaka, Rie
Kikuta, Shingo
Shimura, Sachiko
Kanamori, Hiroyuki
Katayose, Yuichi
Matsumoto, Takashi
Shagimardanova, Elena
Alexeev, Dmitry
Govorun, Vadim
Wisecaver, Jennifer
Mikheyev, Alexander
Koyanagi, Ryo
Fujie, Manabu
Nishiyama, Tomoaki
Shigenobu, Shuji
Shibata, Tomoko F.
Golygina, Veronika
Hasebe, Mitsuyasu
Okuda, Takashi
Satoh, Nori
Kikawada, Takahiro
author_facet Gusev, Oleg
Suetsugu, Yoshitaka
Cornette, Richard
Kawashima, Takeshi
Logacheva, Maria D.
Kondrashov, Alexey S.
Penin, Aleksey A.
Hatanaka, Rie
Kikuta, Shingo
Shimura, Sachiko
Kanamori, Hiroyuki
Katayose, Yuichi
Matsumoto, Takashi
Shagimardanova, Elena
Alexeev, Dmitry
Govorun, Vadim
Wisecaver, Jennifer
Mikheyev, Alexander
Koyanagi, Ryo
Fujie, Manabu
Nishiyama, Tomoaki
Shigenobu, Shuji
Shibata, Tomoko F.
Golygina, Veronika
Hasebe, Mitsuyasu
Okuda, Takashi
Satoh, Nori
Kikawada, Takahiro
author_sort Gusev, Oleg
collection PubMed
description Anhydrobiosis represents an extreme example of tolerance adaptation to water loss, where an organism can survive in an ametabolic state until water returns. Here we report the first comparative analysis examining the genomic background of extreme desiccation tolerance, which is exclusively found in larvae of the only anhydrobiotic insect, Polypedilum vanderplanki. We compare the genomes of P. vanderplanki and a congeneric desiccation-sensitive midge P. nubifer. We determine that the genome of the anhydrobiotic species specifically contains clusters of multi-copy genes with products that act as molecular shields. In addition, the genome possesses several groups of genes with high similarity to known protective proteins. However, these genes are located in distinct paralogous clusters in the genome apart from the classical orthologues of the corresponding genes shared by both chironomids and other insects. The transcripts of these clustered paralogues contribute to a large majority of the mRNA pool in the desiccating larvae and most likely define successful anhydrobiosis. Comparison of expression patterns of orthologues between two chironomid species provides evidence for the existence of desiccation-specific gene expression systems in P. vanderplanki.
format Online
Article
Text
id pubmed-4175575
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Nature Pub. Group
record_format MEDLINE/PubMed
spelling pubmed-41755752014-10-02 Comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge Gusev, Oleg Suetsugu, Yoshitaka Cornette, Richard Kawashima, Takeshi Logacheva, Maria D. Kondrashov, Alexey S. Penin, Aleksey A. Hatanaka, Rie Kikuta, Shingo Shimura, Sachiko Kanamori, Hiroyuki Katayose, Yuichi Matsumoto, Takashi Shagimardanova, Elena Alexeev, Dmitry Govorun, Vadim Wisecaver, Jennifer Mikheyev, Alexander Koyanagi, Ryo Fujie, Manabu Nishiyama, Tomoaki Shigenobu, Shuji Shibata, Tomoko F. Golygina, Veronika Hasebe, Mitsuyasu Okuda, Takashi Satoh, Nori Kikawada, Takahiro Nat Commun Article Anhydrobiosis represents an extreme example of tolerance adaptation to water loss, where an organism can survive in an ametabolic state until water returns. Here we report the first comparative analysis examining the genomic background of extreme desiccation tolerance, which is exclusively found in larvae of the only anhydrobiotic insect, Polypedilum vanderplanki. We compare the genomes of P. vanderplanki and a congeneric desiccation-sensitive midge P. nubifer. We determine that the genome of the anhydrobiotic species specifically contains clusters of multi-copy genes with products that act as molecular shields. In addition, the genome possesses several groups of genes with high similarity to known protective proteins. However, these genes are located in distinct paralogous clusters in the genome apart from the classical orthologues of the corresponding genes shared by both chironomids and other insects. The transcripts of these clustered paralogues contribute to a large majority of the mRNA pool in the desiccating larvae and most likely define successful anhydrobiosis. Comparison of expression patterns of orthologues between two chironomid species provides evidence for the existence of desiccation-specific gene expression systems in P. vanderplanki. Nature Pub. Group 2014-09-12 /pmc/articles/PMC4175575/ /pubmed/25216354 http://dx.doi.org/10.1038/ncomms5784 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Article
Gusev, Oleg
Suetsugu, Yoshitaka
Cornette, Richard
Kawashima, Takeshi
Logacheva, Maria D.
Kondrashov, Alexey S.
Penin, Aleksey A.
Hatanaka, Rie
Kikuta, Shingo
Shimura, Sachiko
Kanamori, Hiroyuki
Katayose, Yuichi
Matsumoto, Takashi
Shagimardanova, Elena
Alexeev, Dmitry
Govorun, Vadim
Wisecaver, Jennifer
Mikheyev, Alexander
Koyanagi, Ryo
Fujie, Manabu
Nishiyama, Tomoaki
Shigenobu, Shuji
Shibata, Tomoko F.
Golygina, Veronika
Hasebe, Mitsuyasu
Okuda, Takashi
Satoh, Nori
Kikawada, Takahiro
Comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge
title Comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge
title_full Comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge
title_fullStr Comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge
title_full_unstemmed Comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge
title_short Comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge
title_sort comparative genome sequencing reveals genomic signature of extreme desiccation tolerance in the anhydrobiotic midge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175575/
https://www.ncbi.nlm.nih.gov/pubmed/25216354
http://dx.doi.org/10.1038/ncomms5784
work_keys_str_mv AT gusevoleg comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT suetsuguyoshitaka comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT cornetterichard comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT kawashimatakeshi comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT logachevamariad comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT kondrashovalexeys comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT peninalekseya comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT hatanakarie comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT kikutashingo comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT shimurasachiko comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT kanamorihiroyuki comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT katayoseyuichi comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT matsumototakashi comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT shagimardanovaelena comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT alexeevdmitry comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT govorunvadim comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT wisecaverjennifer comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT mikheyevalexander comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT koyanagiryo comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT fujiemanabu comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT nishiyamatomoaki comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT shigenobushuji comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT shibatatomokof comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT golyginaveronika comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT hasebemitsuyasu comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT okudatakashi comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT satohnori comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge
AT kikawadatakahiro comparativegenomesequencingrevealsgenomicsignatureofextremedesiccationtoleranceintheanhydrobioticmidge