Cargando…
CG and CHG Methylation Contribute to the Transcriptional Control of OsPRR37-Output Genes in Rice
Plant circadian clock coordinates endogenous transcriptional rhythms with diurnal changes of environmental cues. OsPRR37, a negative component in the rice circadian clock, reportedly regulates transcriptome rhythms, and agronomically important traits. However, the underlying regulatory mechanisms of...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885545/ https://www.ncbi.nlm.nih.gov/pubmed/35242159 http://dx.doi.org/10.3389/fpls.2022.839457 |
_version_ | 1784660447483396096 |
---|---|
author | Liu, Chuan Li, Na Lu, Zeping Sun, Qianxi Pang, Xinhan Xiang, Xudong Deng, Changhao Xiong, Zhengshuojian Shu, Kunxian Yang, Fang Hu, Zhongli |
author_facet | Liu, Chuan Li, Na Lu, Zeping Sun, Qianxi Pang, Xinhan Xiang, Xudong Deng, Changhao Xiong, Zhengshuojian Shu, Kunxian Yang, Fang Hu, Zhongli |
author_sort | Liu, Chuan |
collection | PubMed |
description | Plant circadian clock coordinates endogenous transcriptional rhythms with diurnal changes of environmental cues. OsPRR37, a negative component in the rice circadian clock, reportedly regulates transcriptome rhythms, and agronomically important traits. However, the underlying regulatory mechanisms of OsPRR37-output genes remain largely unknown. In this study, whole genome bisulfite sequencing and high-throughput RNA sequencing were applied to verify the role of DNA methylation in the transcriptional control of OsPRR37-output genes. We found that the overexpression of OsPRR37 suppressed rice growth and altered cytosine methylations in CG and CHG sequence contexts in but not the CHH context (H represents A, T, or C). In total, 35 overlapping genes were identified, and 25 of them showed negative correlation between the methylation level and gene expression. The promoter of the hexokinase gene OsHXK1 was hypomethylated at both CG and CHG sites, and the expression of OsHXK1 was significantly increased. Meanwhile, the leaf starch content was consistently lower in OsPRR37 overexpression lines than in the recipient parent Guangluai 4. Further analysis with published data of time-course transcriptomes revealed that most overlapping genes showed peak expression phases from dusk to dawn. The genes involved in DNA methylation, methylation maintenance, and DNA demethylation were found to be actively expressed around dusk. A DNA glycosylase, namely ROS1A/DNG702, was probably the upstream candidate that demethylated the promoter of OsHXK1. Taken together, our results revealed that CG and CHG methylation contribute to the transcriptional regulation of OsPRR37-output genes, and hypomethylation of OsHXK1 leads to decreased starch content and reduced plant growth in rice. |
format | Online Article Text |
id | pubmed-8885545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88855452022-03-02 CG and CHG Methylation Contribute to the Transcriptional Control of OsPRR37-Output Genes in Rice Liu, Chuan Li, Na Lu, Zeping Sun, Qianxi Pang, Xinhan Xiang, Xudong Deng, Changhao Xiong, Zhengshuojian Shu, Kunxian Yang, Fang Hu, Zhongli Front Plant Sci Plant Science Plant circadian clock coordinates endogenous transcriptional rhythms with diurnal changes of environmental cues. OsPRR37, a negative component in the rice circadian clock, reportedly regulates transcriptome rhythms, and agronomically important traits. However, the underlying regulatory mechanisms of OsPRR37-output genes remain largely unknown. In this study, whole genome bisulfite sequencing and high-throughput RNA sequencing were applied to verify the role of DNA methylation in the transcriptional control of OsPRR37-output genes. We found that the overexpression of OsPRR37 suppressed rice growth and altered cytosine methylations in CG and CHG sequence contexts in but not the CHH context (H represents A, T, or C). In total, 35 overlapping genes were identified, and 25 of them showed negative correlation between the methylation level and gene expression. The promoter of the hexokinase gene OsHXK1 was hypomethylated at both CG and CHG sites, and the expression of OsHXK1 was significantly increased. Meanwhile, the leaf starch content was consistently lower in OsPRR37 overexpression lines than in the recipient parent Guangluai 4. Further analysis with published data of time-course transcriptomes revealed that most overlapping genes showed peak expression phases from dusk to dawn. The genes involved in DNA methylation, methylation maintenance, and DNA demethylation were found to be actively expressed around dusk. A DNA glycosylase, namely ROS1A/DNG702, was probably the upstream candidate that demethylated the promoter of OsHXK1. Taken together, our results revealed that CG and CHG methylation contribute to the transcriptional regulation of OsPRR37-output genes, and hypomethylation of OsHXK1 leads to decreased starch content and reduced plant growth in rice. Frontiers Media S.A. 2022-02-15 /pmc/articles/PMC8885545/ /pubmed/35242159 http://dx.doi.org/10.3389/fpls.2022.839457 Text en Copyright © 2022 Liu, Li, Lu, Sun, Pang, Xiang, Deng, Xiong, Shu, Yang and Hu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Liu, Chuan Li, Na Lu, Zeping Sun, Qianxi Pang, Xinhan Xiang, Xudong Deng, Changhao Xiong, Zhengshuojian Shu, Kunxian Yang, Fang Hu, Zhongli CG and CHG Methylation Contribute to the Transcriptional Control of OsPRR37-Output Genes in Rice |
title | CG and CHG Methylation Contribute to the Transcriptional Control of OsPRR37-Output Genes in Rice |
title_full | CG and CHG Methylation Contribute to the Transcriptional Control of OsPRR37-Output Genes in Rice |
title_fullStr | CG and CHG Methylation Contribute to the Transcriptional Control of OsPRR37-Output Genes in Rice |
title_full_unstemmed | CG and CHG Methylation Contribute to the Transcriptional Control of OsPRR37-Output Genes in Rice |
title_short | CG and CHG Methylation Contribute to the Transcriptional Control of OsPRR37-Output Genes in Rice |
title_sort | cg and chg methylation contribute to the transcriptional control of osprr37-output genes in rice |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885545/ https://www.ncbi.nlm.nih.gov/pubmed/35242159 http://dx.doi.org/10.3389/fpls.2022.839457 |
work_keys_str_mv | AT liuchuan cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT lina cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT luzeping cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT sunqianxi cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT pangxinhan cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT xiangxudong cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT dengchanghao cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT xiongzhengshuojian cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT shukunxian cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT yangfang cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice AT huzhongli cgandchgmethylationcontributetothetranscriptionalcontrolofosprr37outputgenesinrice |