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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...

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Autores principales: Panda, Kaushik, Ji, Lexiang, Neumann, Drexel A., Daron, Josquin, Schmitz, Robert J., Slotkin, R. Keith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
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.
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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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