Cargando…

Methylome decoding of RdDM-mediated reprogramming effects in the Arabidopsis MSH1 system

BACKGROUND: Plants undergo programmed chromatin changes in response to environment, influencing heritable phenotypic plasticity. The RNA-directed DNA methylation (RdDM) pathway is an essential component of this reprogramming process. The relationship of epigenomic changes to gene networks on a genom...

Descripción completa

Detalles Bibliográficos
Autores principales: Kundariya, Hardik, Sanchez, Robersy, Yang, Xiaodong, Hafner, Alenka, Mackenzie, Sally A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351182/
https://www.ncbi.nlm.nih.gov/pubmed/35927734
http://dx.doi.org/10.1186/s13059-022-02731-w
_version_ 1784762386846056448
author Kundariya, Hardik
Sanchez, Robersy
Yang, Xiaodong
Hafner, Alenka
Mackenzie, Sally A.
author_facet Kundariya, Hardik
Sanchez, Robersy
Yang, Xiaodong
Hafner, Alenka
Mackenzie, Sally A.
author_sort Kundariya, Hardik
collection PubMed
description BACKGROUND: Plants undergo programmed chromatin changes in response to environment, influencing heritable phenotypic plasticity. The RNA-directed DNA methylation (RdDM) pathway is an essential component of this reprogramming process. The relationship of epigenomic changes to gene networks on a genome-wide basis has been elusive, particularly for intragenic DNA methylation repatterning. RESULTS: Epigenomic reprogramming is tractable to detailed study and cross-species modeling in the MSH1 system, where perturbation of the plant-specific gene MSH1 triggers at least four distinct nongenetic states to impact plant stress response and growth vigor. Within this system, we have defined RdDM target loci toward decoding phenotype-relevant methylome data. We analyze intragenic methylome repatterning associated with phenotype transitions, identifying state-specific cytosine methylation changes in pivotal growth-versus-stress, chromatin remodeling, and RNA spliceosome gene networks that encompass 871 genes. Over 77% of these genes, and 81% of their central network hubs, are functionally confirmed as RdDM targets based on analysis of mutant datasets and sRNA cluster associations. These dcl2/dcl3/dcl4-sensitive gene methylation sites, many present as singular cytosines, reside within identifiable sequence motifs. These data reflect intragenic methylation repatterning that is targeted and amenable to prediction. CONCLUSIONS: A prevailing assumption that biologically relevant DNA methylation variation occurs predominantly in density-defined differentially methylated regions overlooks behavioral features of intragenic, single-site cytosine methylation variation. RdDM-dependent methylation changes within identifiable sequence motifs reveal gene hubs within networks discriminating stress response and growth vigor epigenetic phenotypes. This study uncovers components of a methylome “code” for de novo intragenic methylation repatterning during plant phenotype transitions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-022-02731-w.
format Online
Article
Text
id pubmed-9351182
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-93511822022-08-05 Methylome decoding of RdDM-mediated reprogramming effects in the Arabidopsis MSH1 system Kundariya, Hardik Sanchez, Robersy Yang, Xiaodong Hafner, Alenka Mackenzie, Sally A. Genome Biol Research BACKGROUND: Plants undergo programmed chromatin changes in response to environment, influencing heritable phenotypic plasticity. The RNA-directed DNA methylation (RdDM) pathway is an essential component of this reprogramming process. The relationship of epigenomic changes to gene networks on a genome-wide basis has been elusive, particularly for intragenic DNA methylation repatterning. RESULTS: Epigenomic reprogramming is tractable to detailed study and cross-species modeling in the MSH1 system, where perturbation of the plant-specific gene MSH1 triggers at least four distinct nongenetic states to impact plant stress response and growth vigor. Within this system, we have defined RdDM target loci toward decoding phenotype-relevant methylome data. We analyze intragenic methylome repatterning associated with phenotype transitions, identifying state-specific cytosine methylation changes in pivotal growth-versus-stress, chromatin remodeling, and RNA spliceosome gene networks that encompass 871 genes. Over 77% of these genes, and 81% of their central network hubs, are functionally confirmed as RdDM targets based on analysis of mutant datasets and sRNA cluster associations. These dcl2/dcl3/dcl4-sensitive gene methylation sites, many present as singular cytosines, reside within identifiable sequence motifs. These data reflect intragenic methylation repatterning that is targeted and amenable to prediction. CONCLUSIONS: A prevailing assumption that biologically relevant DNA methylation variation occurs predominantly in density-defined differentially methylated regions overlooks behavioral features of intragenic, single-site cytosine methylation variation. RdDM-dependent methylation changes within identifiable sequence motifs reveal gene hubs within networks discriminating stress response and growth vigor epigenetic phenotypes. This study uncovers components of a methylome “code” for de novo intragenic methylation repatterning during plant phenotype transitions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-022-02731-w. BioMed Central 2022-08-04 /pmc/articles/PMC9351182/ /pubmed/35927734 http://dx.doi.org/10.1186/s13059-022-02731-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kundariya, Hardik
Sanchez, Robersy
Yang, Xiaodong
Hafner, Alenka
Mackenzie, Sally A.
Methylome decoding of RdDM-mediated reprogramming effects in the Arabidopsis MSH1 system
title Methylome decoding of RdDM-mediated reprogramming effects in the Arabidopsis MSH1 system
title_full Methylome decoding of RdDM-mediated reprogramming effects in the Arabidopsis MSH1 system
title_fullStr Methylome decoding of RdDM-mediated reprogramming effects in the Arabidopsis MSH1 system
title_full_unstemmed Methylome decoding of RdDM-mediated reprogramming effects in the Arabidopsis MSH1 system
title_short Methylome decoding of RdDM-mediated reprogramming effects in the Arabidopsis MSH1 system
title_sort methylome decoding of rddm-mediated reprogramming effects in the arabidopsis msh1 system
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351182/
https://www.ncbi.nlm.nih.gov/pubmed/35927734
http://dx.doi.org/10.1186/s13059-022-02731-w
work_keys_str_mv AT kundariyahardik methylomedecodingofrddmmediatedreprogrammingeffectsinthearabidopsismsh1system
AT sanchezrobersy methylomedecodingofrddmmediatedreprogrammingeffectsinthearabidopsismsh1system
AT yangxiaodong methylomedecodingofrddmmediatedreprogrammingeffectsinthearabidopsismsh1system
AT hafneralenka methylomedecodingofrddmmediatedreprogrammingeffectsinthearabidopsismsh1system
AT mackenziesallya methylomedecodingofrddmmediatedreprogrammingeffectsinthearabidopsismsh1system