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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...

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Autores principales: Liu, Chuan, Li, Na, Lu, Zeping, Sun, Qianxi, Pang, Xinhan, Xiang, Xudong, Deng, Changhao, Xiong, Zhengshuojian, Shu, Kunxian, Yang, Fang, Hu, Zhongli
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
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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.
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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
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