Cargando…

The Methylation Patterns and Transcriptional Responses to Chilling Stress at the Seedling Stage in Rice

Chilling stress is considered the major abiotic stress affecting the growth, development, and yield of rice. To understand the transcriptomic responses and methylation regulation of rice in response to chilling stress, we analyzed a cold-tolerant variety of rice (Oryza sativa L. cv. P427). The physi...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Hui, Wu, Tingkai, Li, Shuxing, He, Qiang, Yang, Zhanlie, Zhang, Wuhan, Gan, Yu, Sun, Pingyong, Xiang, Guanlun, Zhang, Hongyu, Deng, Huafeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829347/
https://www.ncbi.nlm.nih.gov/pubmed/31615063
http://dx.doi.org/10.3390/ijms20205089
_version_ 1783465533680648192
author Guo, Hui
Wu, Tingkai
Li, Shuxing
He, Qiang
Yang, Zhanlie
Zhang, Wuhan
Gan, Yu
Sun, Pingyong
Xiang, Guanlun
Zhang, Hongyu
Deng, Huafeng
author_facet Guo, Hui
Wu, Tingkai
Li, Shuxing
He, Qiang
Yang, Zhanlie
Zhang, Wuhan
Gan, Yu
Sun, Pingyong
Xiang, Guanlun
Zhang, Hongyu
Deng, Huafeng
author_sort Guo, Hui
collection PubMed
description Chilling stress is considered the major abiotic stress affecting the growth, development, and yield of rice. To understand the transcriptomic responses and methylation regulation of rice in response to chilling stress, we analyzed a cold-tolerant variety of rice (Oryza sativa L. cv. P427). The physiological properties, transcriptome, and methylation of cold-tolerant P427 seedlings under low-temperature stress (2–3 °C) were investigated. We found that P427 exhibited enhanced tolerance to low temperature, likely via increasing antioxidant enzyme activity and promoting the accumulation of abscisic acid (ABA). The Methylated DNA Immunoprecipitation Sequencing (MeDIP-seq) data showed that the number of methylation-altered genes was highest in P427 (5496) and slightly lower in Nipponbare (Nip) and 9311 (4528 and 3341, respectively), and only 2.7% (292) of methylation genes were detected as common differentially methylated genes (DMGs) related to cold tolerance in the three varieties. Transcriptome analyses revealed that 1654 genes had specifically altered expression in P427 under cold stress. These genes mainly belonged to transcription factor families, such as Myeloblastosis (MYB), APETALA2/ethylene-responsive element binding proteins (AP2-EREBP), NAM-ATAF-CUC (NAC) and WRKY. Fifty-one genes showed simultaneous methylation and expression level changes. Quantitative RT-PCR (qRT-PCR) results showed that genes involved in the ICE (inducer of CBF expression)-CBF (C-repeat binding factor)—COR (cold-regulated) pathway were highly expressed under cold stress, including the WRKY genes. The homologous gene Os03g0610900 of the open stomatal 1 (OST1) in rice was obtained by evolutionary tree analysis. Methylation in Os03g0610900 gene promoter region decreased, and the expression level of Os03g0610900 increased, suggesting that cold stress may lead to demethylation and increased gene expression of Os03g0610900. The ICE-CBF-COR pathway plays a vital role in the cold tolerance of the rice cultivar P427. Overall, this study demonstrates the differences in methylation and gene expression levels of P427 in response to low-temperature stress, providing a foundation for further investigations of the relationship between environmental stress, DNA methylation, and gene expression in rice.
format Online
Article
Text
id pubmed-6829347
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-68293472019-11-18 The Methylation Patterns and Transcriptional Responses to Chilling Stress at the Seedling Stage in Rice Guo, Hui Wu, Tingkai Li, Shuxing He, Qiang Yang, Zhanlie Zhang, Wuhan Gan, Yu Sun, Pingyong Xiang, Guanlun Zhang, Hongyu Deng, Huafeng Int J Mol Sci Article Chilling stress is considered the major abiotic stress affecting the growth, development, and yield of rice. To understand the transcriptomic responses and methylation regulation of rice in response to chilling stress, we analyzed a cold-tolerant variety of rice (Oryza sativa L. cv. P427). The physiological properties, transcriptome, and methylation of cold-tolerant P427 seedlings under low-temperature stress (2–3 °C) were investigated. We found that P427 exhibited enhanced tolerance to low temperature, likely via increasing antioxidant enzyme activity and promoting the accumulation of abscisic acid (ABA). The Methylated DNA Immunoprecipitation Sequencing (MeDIP-seq) data showed that the number of methylation-altered genes was highest in P427 (5496) and slightly lower in Nipponbare (Nip) and 9311 (4528 and 3341, respectively), and only 2.7% (292) of methylation genes were detected as common differentially methylated genes (DMGs) related to cold tolerance in the three varieties. Transcriptome analyses revealed that 1654 genes had specifically altered expression in P427 under cold stress. These genes mainly belonged to transcription factor families, such as Myeloblastosis (MYB), APETALA2/ethylene-responsive element binding proteins (AP2-EREBP), NAM-ATAF-CUC (NAC) and WRKY. Fifty-one genes showed simultaneous methylation and expression level changes. Quantitative RT-PCR (qRT-PCR) results showed that genes involved in the ICE (inducer of CBF expression)-CBF (C-repeat binding factor)—COR (cold-regulated) pathway were highly expressed under cold stress, including the WRKY genes. The homologous gene Os03g0610900 of the open stomatal 1 (OST1) in rice was obtained by evolutionary tree analysis. Methylation in Os03g0610900 gene promoter region decreased, and the expression level of Os03g0610900 increased, suggesting that cold stress may lead to demethylation and increased gene expression of Os03g0610900. The ICE-CBF-COR pathway plays a vital role in the cold tolerance of the rice cultivar P427. Overall, this study demonstrates the differences in methylation and gene expression levels of P427 in response to low-temperature stress, providing a foundation for further investigations of the relationship between environmental stress, DNA methylation, and gene expression in rice. MDPI 2019-10-14 /pmc/articles/PMC6829347/ /pubmed/31615063 http://dx.doi.org/10.3390/ijms20205089 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Guo, Hui
Wu, Tingkai
Li, Shuxing
He, Qiang
Yang, Zhanlie
Zhang, Wuhan
Gan, Yu
Sun, Pingyong
Xiang, Guanlun
Zhang, Hongyu
Deng, Huafeng
The Methylation Patterns and Transcriptional Responses to Chilling Stress at the Seedling Stage in Rice
title The Methylation Patterns and Transcriptional Responses to Chilling Stress at the Seedling Stage in Rice
title_full The Methylation Patterns and Transcriptional Responses to Chilling Stress at the Seedling Stage in Rice
title_fullStr The Methylation Patterns and Transcriptional Responses to Chilling Stress at the Seedling Stage in Rice
title_full_unstemmed The Methylation Patterns and Transcriptional Responses to Chilling Stress at the Seedling Stage in Rice
title_short The Methylation Patterns and Transcriptional Responses to Chilling Stress at the Seedling Stage in Rice
title_sort methylation patterns and transcriptional responses to chilling stress at the seedling stage in rice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829347/
https://www.ncbi.nlm.nih.gov/pubmed/31615063
http://dx.doi.org/10.3390/ijms20205089
work_keys_str_mv AT guohui themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT wutingkai themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT lishuxing themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT heqiang themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT yangzhanlie themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT zhangwuhan themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT ganyu themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT sunpingyong themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT xiangguanlun themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT zhanghongyu themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT denghuafeng themethylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT guohui methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT wutingkai methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT lishuxing methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT heqiang methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT yangzhanlie methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT zhangwuhan methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT ganyu methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT sunpingyong methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT xiangguanlun methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT zhanghongyu methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice
AT denghuafeng methylationpatternsandtranscriptionalresponsestochillingstressattheseedlingstageinrice