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How a Retrotransposon Exploits the Plant's Heat Stress Response for Its Activation

Retrotransposons are major components of plant and animal genomes. They amplify by reverse transcription and reintegration into the host genome but their activity is usually epigenetically silenced. In plants, genomic copies of retrotransposons are typically associated with repressive chromatin modi...

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Autores principales: Cavrak, Vladimir V., Lettner, Nicole, Jamge, Suraj, Kosarewicz, Agata, Bayer, Laura Maria, Mittelsten Scheid, Ortrun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907296/
https://www.ncbi.nlm.nih.gov/pubmed/24497839
http://dx.doi.org/10.1371/journal.pgen.1004115
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author Cavrak, Vladimir V.
Lettner, Nicole
Jamge, Suraj
Kosarewicz, Agata
Bayer, Laura Maria
Mittelsten Scheid, Ortrun
author_facet Cavrak, Vladimir V.
Lettner, Nicole
Jamge, Suraj
Kosarewicz, Agata
Bayer, Laura Maria
Mittelsten Scheid, Ortrun
author_sort Cavrak, Vladimir V.
collection PubMed
description Retrotransposons are major components of plant and animal genomes. They amplify by reverse transcription and reintegration into the host genome but their activity is usually epigenetically silenced. In plants, genomic copies of retrotransposons are typically associated with repressive chromatin modifications installed and maintained by RNA-directed DNA methylation. To escape this tight control, retrotransposons employ various strategies to avoid epigenetic silencing. Here we describe the mechanism developed by ONSEN, an LTR-copia type retrotransposon in Arabidopsis thaliana. ONSEN has acquired a heat-responsive element recognized by plant-derived heat stress defense factors, resulting in transcription and production of full length extrachromosomal DNA under elevated temperatures. Further, the ONSEN promoter is free of CG and CHG sites, and the reduction of DNA methylation at the CHH sites is not sufficient to activate the element. Since dividing cells have a more pronounced heat response, the extrachromosomal ONSEN DNA, capable of reintegrating into the genome, accumulates preferentially in the meristematic tissue of the shoot. The recruitment of a major plant heat shock transcription factor in periods of heat stress exploits the plant's heat stress response to achieve the transposon's activation, making it impossible for the host to respond appropriately to stress without losing control over the invader.
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spelling pubmed-39072962014-02-04 How a Retrotransposon Exploits the Plant's Heat Stress Response for Its Activation Cavrak, Vladimir V. Lettner, Nicole Jamge, Suraj Kosarewicz, Agata Bayer, Laura Maria Mittelsten Scheid, Ortrun PLoS Genet Research Article Retrotransposons are major components of plant and animal genomes. They amplify by reverse transcription and reintegration into the host genome but their activity is usually epigenetically silenced. In plants, genomic copies of retrotransposons are typically associated with repressive chromatin modifications installed and maintained by RNA-directed DNA methylation. To escape this tight control, retrotransposons employ various strategies to avoid epigenetic silencing. Here we describe the mechanism developed by ONSEN, an LTR-copia type retrotransposon in Arabidopsis thaliana. ONSEN has acquired a heat-responsive element recognized by plant-derived heat stress defense factors, resulting in transcription and production of full length extrachromosomal DNA under elevated temperatures. Further, the ONSEN promoter is free of CG and CHG sites, and the reduction of DNA methylation at the CHH sites is not sufficient to activate the element. Since dividing cells have a more pronounced heat response, the extrachromosomal ONSEN DNA, capable of reintegrating into the genome, accumulates preferentially in the meristematic tissue of the shoot. The recruitment of a major plant heat shock transcription factor in periods of heat stress exploits the plant's heat stress response to achieve the transposon's activation, making it impossible for the host to respond appropriately to stress without losing control over the invader. Public Library of Science 2014-01-30 /pmc/articles/PMC3907296/ /pubmed/24497839 http://dx.doi.org/10.1371/journal.pgen.1004115 Text en © 2014 Cavrak et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cavrak, Vladimir V.
Lettner, Nicole
Jamge, Suraj
Kosarewicz, Agata
Bayer, Laura Maria
Mittelsten Scheid, Ortrun
How a Retrotransposon Exploits the Plant's Heat Stress Response for Its Activation
title How a Retrotransposon Exploits the Plant's Heat Stress Response for Its Activation
title_full How a Retrotransposon Exploits the Plant's Heat Stress Response for Its Activation
title_fullStr How a Retrotransposon Exploits the Plant's Heat Stress Response for Its Activation
title_full_unstemmed How a Retrotransposon Exploits the Plant's Heat Stress Response for Its Activation
title_short How a Retrotransposon Exploits the Plant's Heat Stress Response for Its Activation
title_sort how a retrotransposon exploits the plant's heat stress response for its activation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907296/
https://www.ncbi.nlm.nih.gov/pubmed/24497839
http://dx.doi.org/10.1371/journal.pgen.1004115
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