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Global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea

Fungal infections are the inevitable limiting factor for productivity of tea. Transcriptome reprogramming recruits multiple regulatory pathways during pathogen infection. A comprehensive meta-analysis was performed utilizing previously reported, well-replicated transcriptomic datasets from seven fun...

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Autores principales: Hazra, Anjan, Ghosh, Sanatan, Naskar, Sudipta, Rahaman, Piya, Roy, Chitralekha, Kundu, Anirban, Chaudhuri, Rituparna Kundu, Chakraborti, Dipankar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567763/
https://www.ncbi.nlm.nih.gov/pubmed/37821523
http://dx.doi.org/10.1038/s41598-023-44163-x
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author Hazra, Anjan
Ghosh, Sanatan
Naskar, Sudipta
Rahaman, Piya
Roy, Chitralekha
Kundu, Anirban
Chaudhuri, Rituparna Kundu
Chakraborti, Dipankar
author_facet Hazra, Anjan
Ghosh, Sanatan
Naskar, Sudipta
Rahaman, Piya
Roy, Chitralekha
Kundu, Anirban
Chaudhuri, Rituparna Kundu
Chakraborti, Dipankar
author_sort Hazra, Anjan
collection PubMed
description Fungal infections are the inevitable limiting factor for productivity of tea. Transcriptome reprogramming recruits multiple regulatory pathways during pathogen infection. A comprehensive meta-analysis was performed utilizing previously reported, well-replicated transcriptomic datasets from seven fungal diseases of tea. The study identified a cumulative set of 18,517 differentially expressed genes (DEGs) in tea, implicated in several functional clusters, including the MAPK signaling pathway, transcriptional regulation, and the biosynthesis of phenylpropanoids. Gene set enrichment analyses under each pathogen stress elucidated that DEGs were involved in ethylene metabolism, secondary metabolism, receptor kinase activity, and various reactive oxygen species detoxification enzyme activities. Expressional fold change of combined datasets highlighting 2258 meta-DEGs shared a common transcriptomic response upon fungal stress in tea. Pervasive duplication events caused biotic stress-responsive core DEGs to appear in multiple copies throughout the tea genome. The co-expression network of meta-DEGs in multiple modules demonstrated the coordination of appropriate pathways, most of which involved cell wall organization. The functional coordination was controlled by a number of hub genes and miRNAs, leading to pathogenic resistance or susceptibility. This first-of-its-kind meta-analysis of host–pathogen interaction generated consensus candidate loci as molecular signatures, which can be associated with future resistance breeding programs in tea.
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spelling pubmed-105677632023-10-13 Global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea Hazra, Anjan Ghosh, Sanatan Naskar, Sudipta Rahaman, Piya Roy, Chitralekha Kundu, Anirban Chaudhuri, Rituparna Kundu Chakraborti, Dipankar Sci Rep Article Fungal infections are the inevitable limiting factor for productivity of tea. Transcriptome reprogramming recruits multiple regulatory pathways during pathogen infection. A comprehensive meta-analysis was performed utilizing previously reported, well-replicated transcriptomic datasets from seven fungal diseases of tea. The study identified a cumulative set of 18,517 differentially expressed genes (DEGs) in tea, implicated in several functional clusters, including the MAPK signaling pathway, transcriptional regulation, and the biosynthesis of phenylpropanoids. Gene set enrichment analyses under each pathogen stress elucidated that DEGs were involved in ethylene metabolism, secondary metabolism, receptor kinase activity, and various reactive oxygen species detoxification enzyme activities. Expressional fold change of combined datasets highlighting 2258 meta-DEGs shared a common transcriptomic response upon fungal stress in tea. Pervasive duplication events caused biotic stress-responsive core DEGs to appear in multiple copies throughout the tea genome. The co-expression network of meta-DEGs in multiple modules demonstrated the coordination of appropriate pathways, most of which involved cell wall organization. The functional coordination was controlled by a number of hub genes and miRNAs, leading to pathogenic resistance or susceptibility. This first-of-its-kind meta-analysis of host–pathogen interaction generated consensus candidate loci as molecular signatures, which can be associated with future resistance breeding programs in tea. Nature Publishing Group UK 2023-10-11 /pmc/articles/PMC10567763/ /pubmed/37821523 http://dx.doi.org/10.1038/s41598-023-44163-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Hazra, Anjan
Ghosh, Sanatan
Naskar, Sudipta
Rahaman, Piya
Roy, Chitralekha
Kundu, Anirban
Chaudhuri, Rituparna Kundu
Chakraborti, Dipankar
Global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea
title Global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea
title_full Global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea
title_fullStr Global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea
title_full_unstemmed Global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea
title_short Global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea
title_sort global transcriptome analysis reveals fungal disease responsive core gene regulatory landscape in tea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567763/
https://www.ncbi.nlm.nih.gov/pubmed/37821523
http://dx.doi.org/10.1038/s41598-023-44163-x
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