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Full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of RNA-directed DNA methylation
BACKGROUND: Chromatin modifications such as DNA methylation are targeted to transposable elements by small RNAs in a process termed RNA-directed DNA methylation (RdDM). In plants, canonical RdDM functions through RNA polymerase IV to reinforce pre-existing transposable element silencing. Recent inve...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977677/ https://www.ncbi.nlm.nih.gov/pubmed/27506905 http://dx.doi.org/10.1186/s13059-016-1032-y |
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author | Panda, Kaushik Ji, Lexiang Neumann, Drexel A. Daron, Josquin Schmitz, Robert J. Slotkin, R. Keith |
author_facet | Panda, Kaushik Ji, Lexiang Neumann, Drexel A. Daron, Josquin Schmitz, Robert J. Slotkin, R. Keith |
author_sort | Panda, Kaushik |
collection | PubMed |
description | BACKGROUND: Chromatin modifications such as DNA methylation are targeted to transposable elements by small RNAs in a process termed RNA-directed DNA methylation (RdDM). In plants, canonical RdDM functions through RNA polymerase IV to reinforce pre-existing transposable element silencing. Recent investigations have identified a “non-canonical” form of RdDM dependent on RNA polymerase II expression to initiate and re-establish silencing of active transposable elements. This expression-dependent RdDM mechanism functions through RNAi degradation of transposable element mRNAs into small RNAs guided by the RNA-dependent RNA polymerase 6 (RDR6) protein and is therefore referred to as RDR6-RdDM. RESULTS: We performed whole-genome MethylC-seq in 20 mutants that distinguish RdDM mechanisms when transposable elements are either transcriptionally silent or active. We identified a new mechanism of expression-dependent RdDM, which functions through DICER-LIKE3 (DCL3) but bypasses the requirement of both RNA polymerase IV and RDR6 (termed DCL3-RdDM). We found that RNA polymerase II expression-dependent forms of RdDM function on over 20 % of transcribed transposable elements, including the majority of full-length elements with all of the domains required for autonomous transposition. Lastly, we find that RDR6-RdDM preferentially targets long transposable elements due to the specificity of primary small RNAs to cleave full-length mRNAs. CONCLUSIONS: Expression-dependent forms of RdDM function to critically target DNA methylation to full-length and transcriptionally active transposable elements, suggesting that these pathways are key to suppressing mobilization. This targeting specificity is initiated on the mRNA cleavage-level, yet manifested as chromatin-level silencing that in plants is epigenetically inherited from generation to generation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1032-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4977677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49776772016-08-10 Full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of RNA-directed DNA methylation Panda, Kaushik Ji, Lexiang Neumann, Drexel A. Daron, Josquin Schmitz, Robert J. Slotkin, R. Keith Genome Biol Research BACKGROUND: Chromatin modifications such as DNA methylation are targeted to transposable elements by small RNAs in a process termed RNA-directed DNA methylation (RdDM). In plants, canonical RdDM functions through RNA polymerase IV to reinforce pre-existing transposable element silencing. Recent investigations have identified a “non-canonical” form of RdDM dependent on RNA polymerase II expression to initiate and re-establish silencing of active transposable elements. This expression-dependent RdDM mechanism functions through RNAi degradation of transposable element mRNAs into small RNAs guided by the RNA-dependent RNA polymerase 6 (RDR6) protein and is therefore referred to as RDR6-RdDM. RESULTS: We performed whole-genome MethylC-seq in 20 mutants that distinguish RdDM mechanisms when transposable elements are either transcriptionally silent or active. We identified a new mechanism of expression-dependent RdDM, which functions through DICER-LIKE3 (DCL3) but bypasses the requirement of both RNA polymerase IV and RDR6 (termed DCL3-RdDM). We found that RNA polymerase II expression-dependent forms of RdDM function on over 20 % of transcribed transposable elements, including the majority of full-length elements with all of the domains required for autonomous transposition. Lastly, we find that RDR6-RdDM preferentially targets long transposable elements due to the specificity of primary small RNAs to cleave full-length mRNAs. CONCLUSIONS: Expression-dependent forms of RdDM function to critically target DNA methylation to full-length and transcriptionally active transposable elements, suggesting that these pathways are key to suppressing mobilization. This targeting specificity is initiated on the mRNA cleavage-level, yet manifested as chromatin-level silencing that in plants is epigenetically inherited from generation to generation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1032-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-09 /pmc/articles/PMC4977677/ /pubmed/27506905 http://dx.doi.org/10.1186/s13059-016-1032-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Panda, Kaushik Ji, Lexiang Neumann, Drexel A. Daron, Josquin Schmitz, Robert J. Slotkin, R. Keith Full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of RNA-directed DNA methylation |
title | Full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of RNA-directed DNA methylation |
title_full | Full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of RNA-directed DNA methylation |
title_fullStr | Full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of RNA-directed DNA methylation |
title_full_unstemmed | Full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of RNA-directed DNA methylation |
title_short | Full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of RNA-directed DNA methylation |
title_sort | full-length autonomous transposable elements are preferentially targeted by expression-dependent forms of rna-directed dna methylation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977677/ https://www.ncbi.nlm.nih.gov/pubmed/27506905 http://dx.doi.org/10.1186/s13059-016-1032-y |
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