Cargando…
Divergent DNA methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response
DNA methylation is an epigenetic mechanism that play an important role in gene regulation in response to environmental conditions. The understanding of DNA methylation at the whole genome level can provide insights into the regulatory mechanisms underlying abiotic stress response/adaptation. We repo...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598828/ https://www.ncbi.nlm.nih.gov/pubmed/26449881 http://dx.doi.org/10.1038/srep14922 |
_version_ | 1782394137619726336 |
---|---|
author | Garg, Rohini Narayana Chevala, VVS Shankar, Rama Jain, Mukesh |
author_facet | Garg, Rohini Narayana Chevala, VVS Shankar, Rama Jain, Mukesh |
author_sort | Garg, Rohini |
collection | PubMed |
description | DNA methylation is an epigenetic mechanism that play an important role in gene regulation in response to environmental conditions. The understanding of DNA methylation at the whole genome level can provide insights into the regulatory mechanisms underlying abiotic stress response/adaptation. We report DNA methylation patterns and their influence on transcription in three rice (Oryza sativa) cultivars (IR64, stress-sensitive; Nagina 22, drought-tolerant; Pokkali, salinity-tolerant) via an integrated analysis of whole genome bisulphite sequencing and RNA sequencing. We discovered extensive DNA methylation at single-base resolution in rice cultivars, identified the sequence context and extent of methylation at each site. Overall, methylation levels were significantly different in the three rice cultivars. Numerous differentially methylated regions (DMRs) among different cultivars were identified and many of which were associated with differential expression of genes important for abiotic stress response. Transposon-associated DMRs were found coupled to the transcript abundance of nearby protein-coding gene(s). Small RNA (smRNA) abundance was found to be positively correlated with hypermethylated regions. These results provide insights into interplay among DNA methylation, gene expression and smRNA abundance, and suggest a role in abiotic stress adaptation in rice. |
format | Online Article Text |
id | pubmed-4598828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45988282015-10-13 Divergent DNA methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response Garg, Rohini Narayana Chevala, VVS Shankar, Rama Jain, Mukesh Sci Rep Article DNA methylation is an epigenetic mechanism that play an important role in gene regulation in response to environmental conditions. The understanding of DNA methylation at the whole genome level can provide insights into the regulatory mechanisms underlying abiotic stress response/adaptation. We report DNA methylation patterns and their influence on transcription in three rice (Oryza sativa) cultivars (IR64, stress-sensitive; Nagina 22, drought-tolerant; Pokkali, salinity-tolerant) via an integrated analysis of whole genome bisulphite sequencing and RNA sequencing. We discovered extensive DNA methylation at single-base resolution in rice cultivars, identified the sequence context and extent of methylation at each site. Overall, methylation levels were significantly different in the three rice cultivars. Numerous differentially methylated regions (DMRs) among different cultivars were identified and many of which were associated with differential expression of genes important for abiotic stress response. Transposon-associated DMRs were found coupled to the transcript abundance of nearby protein-coding gene(s). Small RNA (smRNA) abundance was found to be positively correlated with hypermethylated regions. These results provide insights into interplay among DNA methylation, gene expression and smRNA abundance, and suggest a role in abiotic stress adaptation in rice. Nature Publishing Group 2015-10-09 /pmc/articles/PMC4598828/ /pubmed/26449881 http://dx.doi.org/10.1038/srep14922 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Garg, Rohini Narayana Chevala, VVS Shankar, Rama Jain, Mukesh Divergent DNA methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response |
title | Divergent DNA methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response |
title_full | Divergent DNA methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response |
title_fullStr | Divergent DNA methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response |
title_full_unstemmed | Divergent DNA methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response |
title_short | Divergent DNA methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response |
title_sort | divergent dna methylation patterns associated with gene expression in rice cultivars with contrasting drought and salinity stress response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598828/ https://www.ncbi.nlm.nih.gov/pubmed/26449881 http://dx.doi.org/10.1038/srep14922 |
work_keys_str_mv | AT gargrohini divergentdnamethylationpatternsassociatedwithgeneexpressioninricecultivarswithcontrastingdroughtandsalinitystressresponse AT narayanachevalavvs divergentdnamethylationpatternsassociatedwithgeneexpressioninricecultivarswithcontrastingdroughtandsalinitystressresponse AT shankarrama divergentdnamethylationpatternsassociatedwithgeneexpressioninricecultivarswithcontrastingdroughtandsalinitystressresponse AT jainmukesh divergentdnamethylationpatternsassociatedwithgeneexpressioninricecultivarswithcontrastingdroughtandsalinitystressresponse |