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Arms race between anti‐silencing and RdDM in noncoding regions of transposable elements
Transposable elements (TEs) are among the most dynamic parts of genomes. Since TEs are potentially deleterious, eukaryotes silence them through epigenetic mechanisms such as repressive histone modifications and DNA methylation. We previously reported that Arabidopsis TEs, called VANDALs, counteract...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398659/ https://www.ncbi.nlm.nih.gov/pubmed/37272687 http://dx.doi.org/10.15252/embr.202256678 |
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author | Sasaki, Taku Kato, Kae Hosaka, Aoi Fu, Yu Toyoda, Atsushi Fujiyama, Asao Tarutani, Yoshiaki Kakutani, Tetsuji |
author_facet | Sasaki, Taku Kato, Kae Hosaka, Aoi Fu, Yu Toyoda, Atsushi Fujiyama, Asao Tarutani, Yoshiaki Kakutani, Tetsuji |
author_sort | Sasaki, Taku |
collection | PubMed |
description | Transposable elements (TEs) are among the most dynamic parts of genomes. Since TEs are potentially deleterious, eukaryotes silence them through epigenetic mechanisms such as repressive histone modifications and DNA methylation. We previously reported that Arabidopsis TEs, called VANDALs, counteract epigenetic silencing through a group of sequence‐specific anti‐silencing proteins, VANCs. VANC proteins bind to noncoding regions of specific VANDAL copies and induce loss of silent chromatin marks. The VANC‐target regions form tandem repeats, which diverge rapidly. Sequence‐specific anti‐silencing allows these TEs to proliferate with minimum host damage. Here, we show that RNA‐directed DNA methylation (RdDM) efficiently targets noncoding regions of VANDAL TEs to silence them de novo. Thus, escape from RdDM could be a primary event leading to the rapid evolution and diversification of sequence‐specific anti‐silencing systems. We propose that this selfish behavior of TEs paradoxically could make them diverse and less harmful to the host. |
format | Online Article Text |
id | pubmed-10398659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103986592023-08-04 Arms race between anti‐silencing and RdDM in noncoding regions of transposable elements Sasaki, Taku Kato, Kae Hosaka, Aoi Fu, Yu Toyoda, Atsushi Fujiyama, Asao Tarutani, Yoshiaki Kakutani, Tetsuji EMBO Rep Articles Transposable elements (TEs) are among the most dynamic parts of genomes. Since TEs are potentially deleterious, eukaryotes silence them through epigenetic mechanisms such as repressive histone modifications and DNA methylation. We previously reported that Arabidopsis TEs, called VANDALs, counteract epigenetic silencing through a group of sequence‐specific anti‐silencing proteins, VANCs. VANC proteins bind to noncoding regions of specific VANDAL copies and induce loss of silent chromatin marks. The VANC‐target regions form tandem repeats, which diverge rapidly. Sequence‐specific anti‐silencing allows these TEs to proliferate with minimum host damage. Here, we show that RNA‐directed DNA methylation (RdDM) efficiently targets noncoding regions of VANDAL TEs to silence them de novo. Thus, escape from RdDM could be a primary event leading to the rapid evolution and diversification of sequence‐specific anti‐silencing systems. We propose that this selfish behavior of TEs paradoxically could make them diverse and less harmful to the host. John Wiley and Sons Inc. 2023-06-05 /pmc/articles/PMC10398659/ /pubmed/37272687 http://dx.doi.org/10.15252/embr.202256678 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Sasaki, Taku Kato, Kae Hosaka, Aoi Fu, Yu Toyoda, Atsushi Fujiyama, Asao Tarutani, Yoshiaki Kakutani, Tetsuji Arms race between anti‐silencing and RdDM in noncoding regions of transposable elements |
title | Arms race between anti‐silencing and RdDM in noncoding regions of transposable elements |
title_full | Arms race between anti‐silencing and RdDM in noncoding regions of transposable elements |
title_fullStr | Arms race between anti‐silencing and RdDM in noncoding regions of transposable elements |
title_full_unstemmed | Arms race between anti‐silencing and RdDM in noncoding regions of transposable elements |
title_short | Arms race between anti‐silencing and RdDM in noncoding regions of transposable elements |
title_sort | arms race between anti‐silencing and rddm in noncoding regions of transposable elements |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398659/ https://www.ncbi.nlm.nih.gov/pubmed/37272687 http://dx.doi.org/10.15252/embr.202256678 |
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