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Identification of Brassica napus small RNAs responsive to infection by a necrotrophic pathogen
BACKGROUND: Small RNAs are short non-coding RNAs that are key gene regulators controlling various biological processes in eukaryotes. Plants may regulate discrete sets of sRNAs in response to pathogen attack. Sclerotinia sclerotiorum is an economically important pathogen affecting hundreds of plant...
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/PMC8356391/ https://www.ncbi.nlm.nih.gov/pubmed/34380425 http://dx.doi.org/10.1186/s12870-021-03148-6 |
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author | Regmi, Roshan Newman, Toby E. Kamphuis, Lars G. Derbyshire, Mark C. |
author_facet | Regmi, Roshan Newman, Toby E. Kamphuis, Lars G. Derbyshire, Mark C. |
author_sort | Regmi, Roshan |
collection | PubMed |
description | BACKGROUND: Small RNAs are short non-coding RNAs that are key gene regulators controlling various biological processes in eukaryotes. Plants may regulate discrete sets of sRNAs in response to pathogen attack. Sclerotinia sclerotiorum is an economically important pathogen affecting hundreds of plant species, including the economically important oilseed B. napus. However, there are limited studies on how regulation of sRNAs occurs in the S. sclerotiorum and B. napus pathosystem. RESULTS: We identified different classes of sRNAs from B. napus using high throughput sequencing of replicated mock and infected samples at 24 h post-inoculation (HPI). Overall, 3999 sRNA loci were highly expressed, of which 730 were significantly upregulated during infection. These 730 up-regulated sRNAs targeted 64 genes, including disease resistance proteins and transcriptional regulators. A total of 73 conserved miRNA families were identified in our dataset. Degradome sequencing identified 2124 cleaved mRNA products from these miRNAs from combined mock and infected samples. Among these, 50 genes were specific to infection. Altogether, 20 conserved miRNAs were differentially expressed and 8 transcripts were cleaved by the differentially expressed miRNAs miR159, miR5139, and miR390, suggesting they may have a role in the S. sclerotiorum response. A miR1885-triggered disease resistance gene-derived secondary sRNA locus was also identified and verified with degradome sequencing. We also found further evidence for silencing of a plant immunity related ethylene response factor gene by a novel sRNA using 5′-RACE and RT-qPCR. CONCLUSIONS: The findings in this study expand the framework for understanding the molecular mechanisms of the S. sclerotiorum and B. napus pathosystem at the sRNA level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03148-6. |
format | Online Article Text |
id | pubmed-8356391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83563912021-08-11 Identification of Brassica napus small RNAs responsive to infection by a necrotrophic pathogen Regmi, Roshan Newman, Toby E. Kamphuis, Lars G. Derbyshire, Mark C. BMC Plant Biol Research Article BACKGROUND: Small RNAs are short non-coding RNAs that are key gene regulators controlling various biological processes in eukaryotes. Plants may regulate discrete sets of sRNAs in response to pathogen attack. Sclerotinia sclerotiorum is an economically important pathogen affecting hundreds of plant species, including the economically important oilseed B. napus. However, there are limited studies on how regulation of sRNAs occurs in the S. sclerotiorum and B. napus pathosystem. RESULTS: We identified different classes of sRNAs from B. napus using high throughput sequencing of replicated mock and infected samples at 24 h post-inoculation (HPI). Overall, 3999 sRNA loci were highly expressed, of which 730 were significantly upregulated during infection. These 730 up-regulated sRNAs targeted 64 genes, including disease resistance proteins and transcriptional regulators. A total of 73 conserved miRNA families were identified in our dataset. Degradome sequencing identified 2124 cleaved mRNA products from these miRNAs from combined mock and infected samples. Among these, 50 genes were specific to infection. Altogether, 20 conserved miRNAs were differentially expressed and 8 transcripts were cleaved by the differentially expressed miRNAs miR159, miR5139, and miR390, suggesting they may have a role in the S. sclerotiorum response. A miR1885-triggered disease resistance gene-derived secondary sRNA locus was also identified and verified with degradome sequencing. We also found further evidence for silencing of a plant immunity related ethylene response factor gene by a novel sRNA using 5′-RACE and RT-qPCR. CONCLUSIONS: The findings in this study expand the framework for understanding the molecular mechanisms of the S. sclerotiorum and B. napus pathosystem at the sRNA level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03148-6. BioMed Central 2021-08-11 /pmc/articles/PMC8356391/ /pubmed/34380425 http://dx.doi.org/10.1186/s12870-021-03148-6 Text en © The Author(s) 2021, corrected publication 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 Regmi, Roshan Newman, Toby E. Kamphuis, Lars G. Derbyshire, Mark C. Identification of Brassica napus small RNAs responsive to infection by a necrotrophic pathogen |
title | Identification of Brassica napus small RNAs responsive to infection by a necrotrophic pathogen |
title_full | Identification of Brassica napus small RNAs responsive to infection by a necrotrophic pathogen |
title_fullStr | Identification of Brassica napus small RNAs responsive to infection by a necrotrophic pathogen |
title_full_unstemmed | Identification of Brassica napus small RNAs responsive to infection by a necrotrophic pathogen |
title_short | Identification of Brassica napus small RNAs responsive to infection by a necrotrophic pathogen |
title_sort | identification of brassica napus small rnas responsive to infection by a necrotrophic pathogen |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356391/ https://www.ncbi.nlm.nih.gov/pubmed/34380425 http://dx.doi.org/10.1186/s12870-021-03148-6 |
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