Cargando…

Recent expansion of heat-activated retrotransposons in the coral symbiont Symbiodinium microadriaticum

Rising sea surface temperature is the main cause of global coral reef decline. Abnormally high temperatures trigger the breakdown of the symbiotic association between corals and their photosynthetic symbionts in the genus Symbiodinium. Higher genetic variation resulting from shorter generation times...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Jit Ern, Cui, Guoxin, Wang, Xin, Liew, Yi Jin, Aranda, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776459/
https://www.ncbi.nlm.nih.gov/pubmed/29053149
http://dx.doi.org/10.1038/ismej.2017.179
_version_ 1783294084185587712
author Chen, Jit Ern
Cui, Guoxin
Wang, Xin
Liew, Yi Jin
Aranda, Manuel
author_facet Chen, Jit Ern
Cui, Guoxin
Wang, Xin
Liew, Yi Jin
Aranda, Manuel
author_sort Chen, Jit Ern
collection PubMed
description Rising sea surface temperature is the main cause of global coral reef decline. Abnormally high temperatures trigger the breakdown of the symbiotic association between corals and their photosynthetic symbionts in the genus Symbiodinium. Higher genetic variation resulting from shorter generation times has previously been proposed to provide increased adaptability to Symbiodinium compared to the host. Retrotransposition is a significant source of genetic variation in eukaryotes and some transposable elements are specifically expressed under adverse environmental conditions. We present transcriptomic and phylogenetic evidence for the existence of heat stress-activated Ty1-copia-type LTR retrotransposons in the coral symbiont Symbiodinium microadriaticum. Genome-wide analyses of emergence patterns of these elements further indicate recent expansion events in the genome of S. microadriaticum. Our findings suggest that acute temperature increases can activate specific retrotransposons in the Symbiodinium genome with potential impacts on the rate of retrotransposition and the generation of genetic variation under heat stress.
format Online
Article
Text
id pubmed-5776459
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-57764592018-02-01 Recent expansion of heat-activated retrotransposons in the coral symbiont Symbiodinium microadriaticum Chen, Jit Ern Cui, Guoxin Wang, Xin Liew, Yi Jin Aranda, Manuel ISME J Short Communication Rising sea surface temperature is the main cause of global coral reef decline. Abnormally high temperatures trigger the breakdown of the symbiotic association between corals and their photosynthetic symbionts in the genus Symbiodinium. Higher genetic variation resulting from shorter generation times has previously been proposed to provide increased adaptability to Symbiodinium compared to the host. Retrotransposition is a significant source of genetic variation in eukaryotes and some transposable elements are specifically expressed under adverse environmental conditions. We present transcriptomic and phylogenetic evidence for the existence of heat stress-activated Ty1-copia-type LTR retrotransposons in the coral symbiont Symbiodinium microadriaticum. Genome-wide analyses of emergence patterns of these elements further indicate recent expansion events in the genome of S. microadriaticum. Our findings suggest that acute temperature increases can activate specific retrotransposons in the Symbiodinium genome with potential impacts on the rate of retrotransposition and the generation of genetic variation under heat stress. Nature Publishing Group 2018-02 2017-10-20 /pmc/articles/PMC5776459/ /pubmed/29053149 http://dx.doi.org/10.1038/ismej.2017.179 Text en Copyright © 2018 The Author(s) https://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/ (https://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Short Communication
Chen, Jit Ern
Cui, Guoxin
Wang, Xin
Liew, Yi Jin
Aranda, Manuel
Recent expansion of heat-activated retrotransposons in the coral symbiont Symbiodinium microadriaticum
title Recent expansion of heat-activated retrotransposons in the coral symbiont Symbiodinium microadriaticum
title_full Recent expansion of heat-activated retrotransposons in the coral symbiont Symbiodinium microadriaticum
title_fullStr Recent expansion of heat-activated retrotransposons in the coral symbiont Symbiodinium microadriaticum
title_full_unstemmed Recent expansion of heat-activated retrotransposons in the coral symbiont Symbiodinium microadriaticum
title_short Recent expansion of heat-activated retrotransposons in the coral symbiont Symbiodinium microadriaticum
title_sort recent expansion of heat-activated retrotransposons in the coral symbiont symbiodinium microadriaticum
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776459/
https://www.ncbi.nlm.nih.gov/pubmed/29053149
http://dx.doi.org/10.1038/ismej.2017.179
work_keys_str_mv AT chenjitern recentexpansionofheatactivatedretrotransposonsinthecoralsymbiontsymbiodiniummicroadriaticum
AT cuiguoxin recentexpansionofheatactivatedretrotransposonsinthecoralsymbiontsymbiodiniummicroadriaticum
AT wangxin recentexpansionofheatactivatedretrotransposonsinthecoralsymbiontsymbiodiniummicroadriaticum
AT liewyijin recentexpansionofheatactivatedretrotransposonsinthecoralsymbiontsymbiodiniummicroadriaticum
AT arandamanuel recentexpansionofheatactivatedretrotransposonsinthecoralsymbiontsymbiodiniummicroadriaticum