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Transcriptome-wide N6-methyladenosine (m(6)A) methylation in watermelon under CGMMV infection
BACKGROUND: Cucumber green mottle mosaic virus (CGMMV) causes substantial global losses in cucurbit crops, especially watermelon. N6-methyladenosine (m(6)A) methylation in RNA is one of the most important post-transcriptional modification mechanisms in eukaryotes. It has been shown to have important...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8574010/ https://www.ncbi.nlm.nih.gov/pubmed/34749644 http://dx.doi.org/10.1186/s12870-021-03289-8 |
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author | He, Yanjun Li, Lili Yao, Yixiu Li, Yulin Zhang, Huiqing Fan, Min |
author_facet | He, Yanjun Li, Lili Yao, Yixiu Li, Yulin Zhang, Huiqing Fan, Min |
author_sort | He, Yanjun |
collection | PubMed |
description | BACKGROUND: Cucumber green mottle mosaic virus (CGMMV) causes substantial global losses in cucurbit crops, especially watermelon. N6-methyladenosine (m(6)A) methylation in RNA is one of the most important post-transcriptional modification mechanisms in eukaryotes. It has been shown to have important regulatory functions in some model plants, but there has been no research regarding m(6)A modifications in watermelon. RESULTS: We measured the global m(6)A level in resistant watermelon after CGMMV infection using a colorimetric method. And the results found that the global m(6)A level significantly decreased in resistant watermelon after CGMMV infection. Specifically, m(6)A libraries were constructed for the resistant watermelon leaves collected 48 h after CGMMV infection and the whole-genome m(6)A-seq were carried out. Numerous m(6)A modified peaks were identified from CGMMV-infected and control (uninfected) samples. The modification distributions and motifs of these m(6)A peaks were highly conserved in watermelon transcripts but the modification was more abundant than in other reported crop plants. In early response to CGMMV infection, 422 differentially methylated genes (DMGs) were identified, most of which were hypomethylated, and probably associated with the increased expression of watermelon m(6)A demethylase gene ClALKBH4B. Gene Ontology (GO) analysis indicated quite a few DMGs were involved in RNA biology and stress responsive pathways. Combined with RNA-seq analysis, there was generally a negative correlation between m(6)A RNA methylation and transcript level in the watermelon transcriptome. Both the m(6)A methylation and transcript levels of 59 modified genes significantly changed in response to CGMMV infection and some were involved in plant immunity. CONCLUSIONS: Our study represents the first comprehensive characterization of m(6)A patterns in the watermelon transcriptome and helps to clarify the roles and regulatory mechanisms of m(6)A modification in watermelon in early responses to CGMMV. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03289-8. |
format | Online Article Text |
id | pubmed-8574010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85740102021-11-08 Transcriptome-wide N6-methyladenosine (m(6)A) methylation in watermelon under CGMMV infection He, Yanjun Li, Lili Yao, Yixiu Li, Yulin Zhang, Huiqing Fan, Min BMC Plant Biol Research Article BACKGROUND: Cucumber green mottle mosaic virus (CGMMV) causes substantial global losses in cucurbit crops, especially watermelon. N6-methyladenosine (m(6)A) methylation in RNA is one of the most important post-transcriptional modification mechanisms in eukaryotes. It has been shown to have important regulatory functions in some model plants, but there has been no research regarding m(6)A modifications in watermelon. RESULTS: We measured the global m(6)A level in resistant watermelon after CGMMV infection using a colorimetric method. And the results found that the global m(6)A level significantly decreased in resistant watermelon after CGMMV infection. Specifically, m(6)A libraries were constructed for the resistant watermelon leaves collected 48 h after CGMMV infection and the whole-genome m(6)A-seq were carried out. Numerous m(6)A modified peaks were identified from CGMMV-infected and control (uninfected) samples. The modification distributions and motifs of these m(6)A peaks were highly conserved in watermelon transcripts but the modification was more abundant than in other reported crop plants. In early response to CGMMV infection, 422 differentially methylated genes (DMGs) were identified, most of which were hypomethylated, and probably associated with the increased expression of watermelon m(6)A demethylase gene ClALKBH4B. Gene Ontology (GO) analysis indicated quite a few DMGs were involved in RNA biology and stress responsive pathways. Combined with RNA-seq analysis, there was generally a negative correlation between m(6)A RNA methylation and transcript level in the watermelon transcriptome. Both the m(6)A methylation and transcript levels of 59 modified genes significantly changed in response to CGMMV infection and some were involved in plant immunity. CONCLUSIONS: Our study represents the first comprehensive characterization of m(6)A patterns in the watermelon transcriptome and helps to clarify the roles and regulatory mechanisms of m(6)A modification in watermelon in early responses to CGMMV. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03289-8. BioMed Central 2021-11-08 /pmc/articles/PMC8574010/ /pubmed/34749644 http://dx.doi.org/10.1186/s12870-021-03289-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article He, Yanjun Li, Lili Yao, Yixiu Li, Yulin Zhang, Huiqing Fan, Min Transcriptome-wide N6-methyladenosine (m(6)A) methylation in watermelon under CGMMV infection |
title | Transcriptome-wide N6-methyladenosine (m(6)A) methylation in watermelon under CGMMV infection |
title_full | Transcriptome-wide N6-methyladenosine (m(6)A) methylation in watermelon under CGMMV infection |
title_fullStr | Transcriptome-wide N6-methyladenosine (m(6)A) methylation in watermelon under CGMMV infection |
title_full_unstemmed | Transcriptome-wide N6-methyladenosine (m(6)A) methylation in watermelon under CGMMV infection |
title_short | Transcriptome-wide N6-methyladenosine (m(6)A) methylation in watermelon under CGMMV infection |
title_sort | transcriptome-wide n6-methyladenosine (m(6)a) methylation in watermelon under cgmmv infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8574010/ https://www.ncbi.nlm.nih.gov/pubmed/34749644 http://dx.doi.org/10.1186/s12870-021-03289-8 |
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