Cargando…
Unique cell-type specific patterns of DNA methylation in the root meristem
DNA methylation is an epigenetic modification that differs between plant organs and tissues, but the extent of variation between cell types is not known. Here, we report single-base resolution whole genome DNA methylomes, mRNA transcriptomes, and small RNA transcriptomes for six cell populations cov...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855458/ https://www.ncbi.nlm.nih.gov/pubmed/27243651 http://dx.doi.org/10.1038/nplants.2016.58 |
_version_ | 1782430368927842304 |
---|---|
author | Kawakatsu, Taiji Stuart, Tim Valdes, Manuel Breakfield, Natalie Schmitz, Robert J. Nery, Joseph R. Urich, Mark A. Han, Xinwei Lister, Ryan Benfey, Philip N. Ecker, Joseph R. |
author_facet | Kawakatsu, Taiji Stuart, Tim Valdes, Manuel Breakfield, Natalie Schmitz, Robert J. Nery, Joseph R. Urich, Mark A. Han, Xinwei Lister, Ryan Benfey, Philip N. Ecker, Joseph R. |
author_sort | Kawakatsu, Taiji |
collection | PubMed |
description | DNA methylation is an epigenetic modification that differs between plant organs and tissues, but the extent of variation between cell types is not known. Here, we report single-base resolution whole genome DNA methylomes, mRNA transcriptomes, and small RNA transcriptomes for six cell populations covering the major cell types of the Arabidopsis root meristem. We identify widespread cell type specific patterns of DNA methylation, especially in the CHH sequence context. The genome of the columella root cap is the most highly methylated Arabidopsis cell characterized to date. It is hypermethylated within transposable elements, accompanied by increased abundance of transcripts encoding RNA-directed DNA methylation (RdDM) pathway components and 24 nt small RNAs. Absence of the nucleosome remodeler DECREASED DNA METHYLATION 1, required for maintenance of DNA methylation, and low abundance of histone transcripts involved in heterochromatin formation suggests a loss of heterochromatin may occur in the columella, thus allowing access of RdDM factors to the whole genome, and producing excess 24 nt small RNAs in this tissue. Together, these maps provide new insights into the epigenomic diversity that exists between distinct plant somatic cell types. |
format | Online Article Text |
id | pubmed-4855458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-48554582016-10-29 Unique cell-type specific patterns of DNA methylation in the root meristem Kawakatsu, Taiji Stuart, Tim Valdes, Manuel Breakfield, Natalie Schmitz, Robert J. Nery, Joseph R. Urich, Mark A. Han, Xinwei Lister, Ryan Benfey, Philip N. Ecker, Joseph R. Nat Plants Article DNA methylation is an epigenetic modification that differs between plant organs and tissues, but the extent of variation between cell types is not known. Here, we report single-base resolution whole genome DNA methylomes, mRNA transcriptomes, and small RNA transcriptomes for six cell populations covering the major cell types of the Arabidopsis root meristem. We identify widespread cell type specific patterns of DNA methylation, especially in the CHH sequence context. The genome of the columella root cap is the most highly methylated Arabidopsis cell characterized to date. It is hypermethylated within transposable elements, accompanied by increased abundance of transcripts encoding RNA-directed DNA methylation (RdDM) pathway components and 24 nt small RNAs. Absence of the nucleosome remodeler DECREASED DNA METHYLATION 1, required for maintenance of DNA methylation, and low abundance of histone transcripts involved in heterochromatin formation suggests a loss of heterochromatin may occur in the columella, thus allowing access of RdDM factors to the whole genome, and producing excess 24 nt small RNAs in this tissue. Together, these maps provide new insights into the epigenomic diversity that exists between distinct plant somatic cell types. 2016-04-29 /pmc/articles/PMC4855458/ /pubmed/27243651 http://dx.doi.org/10.1038/nplants.2016.58 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Kawakatsu, Taiji Stuart, Tim Valdes, Manuel Breakfield, Natalie Schmitz, Robert J. Nery, Joseph R. Urich, Mark A. Han, Xinwei Lister, Ryan Benfey, Philip N. Ecker, Joseph R. Unique cell-type specific patterns of DNA methylation in the root meristem |
title | Unique cell-type specific patterns of DNA methylation in the root
meristem |
title_full | Unique cell-type specific patterns of DNA methylation in the root
meristem |
title_fullStr | Unique cell-type specific patterns of DNA methylation in the root
meristem |
title_full_unstemmed | Unique cell-type specific patterns of DNA methylation in the root
meristem |
title_short | Unique cell-type specific patterns of DNA methylation in the root
meristem |
title_sort | unique cell-type specific patterns of dna methylation in the root
meristem |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855458/ https://www.ncbi.nlm.nih.gov/pubmed/27243651 http://dx.doi.org/10.1038/nplants.2016.58 |
work_keys_str_mv | AT kawakatsutaiji uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT stuarttim uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT valdesmanuel uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT breakfieldnatalie uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT schmitzrobertj uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT neryjosephr uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT urichmarka uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT hanxinwei uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT listerryan uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT benfeyphilipn uniquecelltypespecificpatternsofdnamethylationintherootmeristem AT eckerjosephr uniquecelltypespecificpatternsofdnamethylationintherootmeristem |