Cargando…

Integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in Cleistogenes songorica, a xerophyte perennial desert plant

BACKGROUND: As global warming continues, heat stress (HS) is becoming an increasingly significant factor limiting plant growth and reproduction, especially for cool-season grass species. The objective of this study was to determine the transcriptional regulatory network of Cleistogenes songorica und...

Descripción completa

Detalles Bibliográficos
Autores principales: Yan, Qi, Zong, Xifang, Wu, Fan, Li, Jie, Ma, Tiantian, Zhao, Yufeng, Ma, Qian, Wang, Penglei, Wang, Yanrong, Zhang, Jiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566159/
https://www.ncbi.nlm.nih.gov/pubmed/33066732
http://dx.doi.org/10.1186/s12864-020-07122-8
_version_ 1783596089032572928
author Yan, Qi
Zong, Xifang
Wu, Fan
Li, Jie
Ma, Tiantian
Zhao, Yufeng
Ma, Qian
Wang, Penglei
Wang, Yanrong
Zhang, Jiyu
author_facet Yan, Qi
Zong, Xifang
Wu, Fan
Li, Jie
Ma, Tiantian
Zhao, Yufeng
Ma, Qian
Wang, Penglei
Wang, Yanrong
Zhang, Jiyu
author_sort Yan, Qi
collection PubMed
description BACKGROUND: As global warming continues, heat stress (HS) is becoming an increasingly significant factor limiting plant growth and reproduction, especially for cool-season grass species. The objective of this study was to determine the transcriptional regulatory network of Cleistogenes songorica under HS via transcriptome profiling, identify of gene families and comparative analysis across major Poaceae species. RESULTS: Physiological analysis revealed significantly decreased leaf relative water content (RWC) but increased proline (Pro) content in C. songorica under 24 h of HS. Transcriptome profiling indicated that 16,028 and 14,645 genes were differentially expressed in the shoots and roots of C. songorica under HS, respectively. Two subgenomes of C. songorica provide equal contribution under HS on the basis of the distribution and expression of differentially expressed genes (DEGs). Furthermore, 216 DEGs were identified as key evolutionarily conserved genes involved in the response to HS in C. songorica via comparative analysis with genes of four Poaceae species; these genes were involved in the ‘response to heat’ and ‘heat acclimation’. Notably, most of the conserved DEGs belonged to the heat-shock protein (HSP) superfamily. Similar results were also obtained from co-expression analysis. Interestingly, hub-genes of co-expression analysis were found to overlap with conserved genes, especially heat-shock protein (HSP). In C. songorica, 84 HSP and 32 heat-shock transcription factor (HSF) genes were identified in the allotetraploid C. songorica genome, and might have undergone purifying selection during evolutionary history based on syntenic and phylogenetic analysis. By analysing the expression patterns of the CsHSPs and CsHSFs, we found that the transcript abundance of 72.7% of the CsHSP genes and of 62.5% of the CsHSF genes changed under heat stress in both the shoots and roots. Finally, a core regulatory network of HS was constructed on the basis of the CsHSP, CsHSF and other responsive genes in C. songorica. CONCLUSIONS: Regulatory network and key genes were comprehensively analysed and identified in C. songorica under HS. This study improves our knowledge of thermotolerance mechanisms in native grasses, and also provides candidate genes for potential applications in the genetic improvement of grasses.
format Online
Article
Text
id pubmed-7566159
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-75661592020-10-20 Integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in Cleistogenes songorica, a xerophyte perennial desert plant Yan, Qi Zong, Xifang Wu, Fan Li, Jie Ma, Tiantian Zhao, Yufeng Ma, Qian Wang, Penglei Wang, Yanrong Zhang, Jiyu BMC Genomics Research Article BACKGROUND: As global warming continues, heat stress (HS) is becoming an increasingly significant factor limiting plant growth and reproduction, especially for cool-season grass species. The objective of this study was to determine the transcriptional regulatory network of Cleistogenes songorica under HS via transcriptome profiling, identify of gene families and comparative analysis across major Poaceae species. RESULTS: Physiological analysis revealed significantly decreased leaf relative water content (RWC) but increased proline (Pro) content in C. songorica under 24 h of HS. Transcriptome profiling indicated that 16,028 and 14,645 genes were differentially expressed in the shoots and roots of C. songorica under HS, respectively. Two subgenomes of C. songorica provide equal contribution under HS on the basis of the distribution and expression of differentially expressed genes (DEGs). Furthermore, 216 DEGs were identified as key evolutionarily conserved genes involved in the response to HS in C. songorica via comparative analysis with genes of four Poaceae species; these genes were involved in the ‘response to heat’ and ‘heat acclimation’. Notably, most of the conserved DEGs belonged to the heat-shock protein (HSP) superfamily. Similar results were also obtained from co-expression analysis. Interestingly, hub-genes of co-expression analysis were found to overlap with conserved genes, especially heat-shock protein (HSP). In C. songorica, 84 HSP and 32 heat-shock transcription factor (HSF) genes were identified in the allotetraploid C. songorica genome, and might have undergone purifying selection during evolutionary history based on syntenic and phylogenetic analysis. By analysing the expression patterns of the CsHSPs and CsHSFs, we found that the transcript abundance of 72.7% of the CsHSP genes and of 62.5% of the CsHSF genes changed under heat stress in both the shoots and roots. Finally, a core regulatory network of HS was constructed on the basis of the CsHSP, CsHSF and other responsive genes in C. songorica. CONCLUSIONS: Regulatory network and key genes were comprehensively analysed and identified in C. songorica under HS. This study improves our knowledge of thermotolerance mechanisms in native grasses, and also provides candidate genes for potential applications in the genetic improvement of grasses. BioMed Central 2020-10-16 /pmc/articles/PMC7566159/ /pubmed/33066732 http://dx.doi.org/10.1186/s12864-020-07122-8 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Yan, Qi
Zong, Xifang
Wu, Fan
Li, Jie
Ma, Tiantian
Zhao, Yufeng
Ma, Qian
Wang, Penglei
Wang, Yanrong
Zhang, Jiyu
Integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in Cleistogenes songorica, a xerophyte perennial desert plant
title Integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in Cleistogenes songorica, a xerophyte perennial desert plant
title_full Integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in Cleistogenes songorica, a xerophyte perennial desert plant
title_fullStr Integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in Cleistogenes songorica, a xerophyte perennial desert plant
title_full_unstemmed Integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in Cleistogenes songorica, a xerophyte perennial desert plant
title_short Integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in Cleistogenes songorica, a xerophyte perennial desert plant
title_sort integrated analysis of co-expression, conserved genes and gene families reveal core regulatory network of heat stress response in cleistogenes songorica, a xerophyte perennial desert plant
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566159/
https://www.ncbi.nlm.nih.gov/pubmed/33066732
http://dx.doi.org/10.1186/s12864-020-07122-8
work_keys_str_mv AT yanqi integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT zongxifang integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT wufan integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT lijie integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT matiantian integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT zhaoyufeng integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT maqian integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT wangpenglei integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT wangyanrong integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant
AT zhangjiyu integratedanalysisofcoexpressionconservedgenesandgenefamiliesrevealcoreregulatorynetworkofheatstressresponseincleistogenessongoricaaxerophyteperennialdesertplant