Cargando…
Genome-Wide Differential DNA Methylation and miRNA Expression Profiling Reveals Epigenetic Regulatory Mechanisms Underlying Nitrogen-Limitation-Triggered Adaptation and Use Efficiency Enhancement in Allotetraploid Rapeseed
Improving crop nitrogen (N) limitation adaptation (NLA) is a core approach to enhance N use efficiency (NUE) and reduce N fertilizer application. Rapeseed has a high demand for N nutrients for optimal plant growth and seed production, but it exhibits low NUE. Epigenetic modification, such as DNA met...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697602/ https://www.ncbi.nlm.nih.gov/pubmed/33182819 http://dx.doi.org/10.3390/ijms21228453 |
_version_ | 1783615634518573056 |
---|---|
author | Hua, Ying-peng Zhou, Ting Huang, Jin-yong Yue, Cai-peng Song, Hai-xing Guan, Chun-yun Zhang, Zhen-hua |
author_facet | Hua, Ying-peng Zhou, Ting Huang, Jin-yong Yue, Cai-peng Song, Hai-xing Guan, Chun-yun Zhang, Zhen-hua |
author_sort | Hua, Ying-peng |
collection | PubMed |
description | Improving crop nitrogen (N) limitation adaptation (NLA) is a core approach to enhance N use efficiency (NUE) and reduce N fertilizer application. Rapeseed has a high demand for N nutrients for optimal plant growth and seed production, but it exhibits low NUE. Epigenetic modification, such as DNA methylation and modification from small RNAs, is key to plant adaptive responses to various stresses. However, epigenetic regulatory mechanisms underlying NLA and NUE remain elusive in allotetraploid B. napus. In this study, we identified overaccumulated carbohydrate, and improved primary and lateral roots in rapeseed plants under N limitation, which resulted in decreased plant nitrate concentrations, enhanced root-to-shoot N translocation, and increased NUE. Transcriptomics and RT-qPCR assays revealed that N limitation induced the expression of NRT1.1, NRT1.5, NRT1.7, NRT2.1/NAR2.1, and Gln1;1, and repressed the transcriptional levels of CLCa, NRT1.8, and NIA1. High-resolution whole genome bisulfite sequencing characterized 5094 differentially methylated genes involving ubiquitin-mediated proteolysis, N recycling, and phytohormone metabolism under N limitation. Hypermethylation/hypomethylation in promoter regions or gene bodies of some key N-metabolism genes might be involved in their transcriptional regulation by N limitation. Genome-wide miRNA sequencing identified 224 N limitation-responsive differentially expressed miRNAs regulating leaf development, amino acid metabolism, and plant hormone signal transduction. Furthermore, degradome sequencing and RT-qPCR assays revealed the miR827-NLA pathway regulating limited N-induced leaf senescence as well as the miR171-SCL6 and miR160-ARF17 pathways regulating root growth under N deficiency. Our study provides a comprehensive insight into the epigenetic regulatory mechanisms underlying rapeseed NLA, and it will be helpful for genetic engineering of NUE in crop species through epigenetic modification of some N metabolism-associated genes. |
format | Online Article Text |
id | pubmed-7697602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76976022020-11-29 Genome-Wide Differential DNA Methylation and miRNA Expression Profiling Reveals Epigenetic Regulatory Mechanisms Underlying Nitrogen-Limitation-Triggered Adaptation and Use Efficiency Enhancement in Allotetraploid Rapeseed Hua, Ying-peng Zhou, Ting Huang, Jin-yong Yue, Cai-peng Song, Hai-xing Guan, Chun-yun Zhang, Zhen-hua Int J Mol Sci Article Improving crop nitrogen (N) limitation adaptation (NLA) is a core approach to enhance N use efficiency (NUE) and reduce N fertilizer application. Rapeseed has a high demand for N nutrients for optimal plant growth and seed production, but it exhibits low NUE. Epigenetic modification, such as DNA methylation and modification from small RNAs, is key to plant adaptive responses to various stresses. However, epigenetic regulatory mechanisms underlying NLA and NUE remain elusive in allotetraploid B. napus. In this study, we identified overaccumulated carbohydrate, and improved primary and lateral roots in rapeseed plants under N limitation, which resulted in decreased plant nitrate concentrations, enhanced root-to-shoot N translocation, and increased NUE. Transcriptomics and RT-qPCR assays revealed that N limitation induced the expression of NRT1.1, NRT1.5, NRT1.7, NRT2.1/NAR2.1, and Gln1;1, and repressed the transcriptional levels of CLCa, NRT1.8, and NIA1. High-resolution whole genome bisulfite sequencing characterized 5094 differentially methylated genes involving ubiquitin-mediated proteolysis, N recycling, and phytohormone metabolism under N limitation. Hypermethylation/hypomethylation in promoter regions or gene bodies of some key N-metabolism genes might be involved in their transcriptional regulation by N limitation. Genome-wide miRNA sequencing identified 224 N limitation-responsive differentially expressed miRNAs regulating leaf development, amino acid metabolism, and plant hormone signal transduction. Furthermore, degradome sequencing and RT-qPCR assays revealed the miR827-NLA pathway regulating limited N-induced leaf senescence as well as the miR171-SCL6 and miR160-ARF17 pathways regulating root growth under N deficiency. Our study provides a comprehensive insight into the epigenetic regulatory mechanisms underlying rapeseed NLA, and it will be helpful for genetic engineering of NUE in crop species through epigenetic modification of some N metabolism-associated genes. MDPI 2020-11-10 /pmc/articles/PMC7697602/ /pubmed/33182819 http://dx.doi.org/10.3390/ijms21228453 Text en © 2020 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 Hua, Ying-peng Zhou, Ting Huang, Jin-yong Yue, Cai-peng Song, Hai-xing Guan, Chun-yun Zhang, Zhen-hua Genome-Wide Differential DNA Methylation and miRNA Expression Profiling Reveals Epigenetic Regulatory Mechanisms Underlying Nitrogen-Limitation-Triggered Adaptation and Use Efficiency Enhancement in Allotetraploid Rapeseed |
title | Genome-Wide Differential DNA Methylation and miRNA Expression Profiling Reveals Epigenetic Regulatory Mechanisms Underlying Nitrogen-Limitation-Triggered Adaptation and Use Efficiency Enhancement in Allotetraploid Rapeseed |
title_full | Genome-Wide Differential DNA Methylation and miRNA Expression Profiling Reveals Epigenetic Regulatory Mechanisms Underlying Nitrogen-Limitation-Triggered Adaptation and Use Efficiency Enhancement in Allotetraploid Rapeseed |
title_fullStr | Genome-Wide Differential DNA Methylation and miRNA Expression Profiling Reveals Epigenetic Regulatory Mechanisms Underlying Nitrogen-Limitation-Triggered Adaptation and Use Efficiency Enhancement in Allotetraploid Rapeseed |
title_full_unstemmed | Genome-Wide Differential DNA Methylation and miRNA Expression Profiling Reveals Epigenetic Regulatory Mechanisms Underlying Nitrogen-Limitation-Triggered Adaptation and Use Efficiency Enhancement in Allotetraploid Rapeseed |
title_short | Genome-Wide Differential DNA Methylation and miRNA Expression Profiling Reveals Epigenetic Regulatory Mechanisms Underlying Nitrogen-Limitation-Triggered Adaptation and Use Efficiency Enhancement in Allotetraploid Rapeseed |
title_sort | genome-wide differential dna methylation and mirna expression profiling reveals epigenetic regulatory mechanisms underlying nitrogen-limitation-triggered adaptation and use efficiency enhancement in allotetraploid rapeseed |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697602/ https://www.ncbi.nlm.nih.gov/pubmed/33182819 http://dx.doi.org/10.3390/ijms21228453 |
work_keys_str_mv | AT huayingpeng genomewidedifferentialdnamethylationandmirnaexpressionprofilingrevealsepigeneticregulatorymechanismsunderlyingnitrogenlimitationtriggeredadaptationanduseefficiencyenhancementinallotetraploidrapeseed AT zhouting genomewidedifferentialdnamethylationandmirnaexpressionprofilingrevealsepigeneticregulatorymechanismsunderlyingnitrogenlimitationtriggeredadaptationanduseefficiencyenhancementinallotetraploidrapeseed AT huangjinyong genomewidedifferentialdnamethylationandmirnaexpressionprofilingrevealsepigeneticregulatorymechanismsunderlyingnitrogenlimitationtriggeredadaptationanduseefficiencyenhancementinallotetraploidrapeseed AT yuecaipeng genomewidedifferentialdnamethylationandmirnaexpressionprofilingrevealsepigeneticregulatorymechanismsunderlyingnitrogenlimitationtriggeredadaptationanduseefficiencyenhancementinallotetraploidrapeseed AT songhaixing genomewidedifferentialdnamethylationandmirnaexpressionprofilingrevealsepigeneticregulatorymechanismsunderlyingnitrogenlimitationtriggeredadaptationanduseefficiencyenhancementinallotetraploidrapeseed AT guanchunyun genomewidedifferentialdnamethylationandmirnaexpressionprofilingrevealsepigeneticregulatorymechanismsunderlyingnitrogenlimitationtriggeredadaptationanduseefficiencyenhancementinallotetraploidrapeseed AT zhangzhenhua genomewidedifferentialdnamethylationandmirnaexpressionprofilingrevealsepigeneticregulatorymechanismsunderlyingnitrogenlimitationtriggeredadaptationanduseefficiencyenhancementinallotetraploidrapeseed |