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Genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes

BACKGROUND: Brassinosteroid (BR) signaling regulates plant growth and development in concert with other signaling pathways. Although many genes have been identified that play a role in BR signaling, the biological and functional consequences of disrupting those key BR genes still require detailed in...

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Autores principales: Seyed Rahmani, Razgar, Shi, Tao, Zhang, Dongzhi, Gou, Xiaoping, Yi, Jing, Miclotte, Giles, Marchal, Kathleen, Li, Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220701/
https://www.ncbi.nlm.nih.gov/pubmed/34157989
http://dx.doi.org/10.1186/s12864-021-07778-w
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author Seyed Rahmani, Razgar
Shi, Tao
Zhang, Dongzhi
Gou, Xiaoping
Yi, Jing
Miclotte, Giles
Marchal, Kathleen
Li, Jia
author_facet Seyed Rahmani, Razgar
Shi, Tao
Zhang, Dongzhi
Gou, Xiaoping
Yi, Jing
Miclotte, Giles
Marchal, Kathleen
Li, Jia
author_sort Seyed Rahmani, Razgar
collection PubMed
description BACKGROUND: Brassinosteroid (BR) signaling regulates plant growth and development in concert with other signaling pathways. Although many genes have been identified that play a role in BR signaling, the biological and functional consequences of disrupting those key BR genes still require detailed investigation. RESULTS: Here we performed phenotypic and transcriptomic comparisons of A. thaliana lines carrying a loss-of-function mutation in BRI1 gene, bri1–5, that exhibits a dwarf phenotype and its three activation-tag suppressor lines that were able to partially revert the bri1–5 mutant phenotype to a WS2 phenotype, namely bri1–5/bri1–1D, bri1–5/brs1–1D, and bri1–5/bak1–1D. From the three investigated bri1–5 suppressors, bri1–5/bak1–1D was the most effective suppressor at the transcriptional level. All three bri1–5 suppressors showed altered expression of the genes in the abscisic acid (ABA signaling) pathway, indicating that ABA likely contributes to the partial recovery of the wild-type phenotype in these bri1–5 suppressors. Network analysis revealed crosstalk between BR and other phytohormone signaling pathways, suggesting that interference with one hormone signaling pathway affects other hormone signaling pathways. In addition, differential expression analysis suggested the existence of a strong negative feedback from BR signaling on BR biosynthesis and also predicted that BRS1, rather than being directly involved in signaling, might be responsible for providing an optimal environment for the interaction between BRI1 and its ligand. CONCLUSIONS: Our study provides insights into the molecular mechanisms and functions of key brassinosteroid (BR) signaling genes, especially BRS1. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07778-w.
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spelling pubmed-82207012021-06-23 Genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes Seyed Rahmani, Razgar Shi, Tao Zhang, Dongzhi Gou, Xiaoping Yi, Jing Miclotte, Giles Marchal, Kathleen Li, Jia BMC Genomics Research Article BACKGROUND: Brassinosteroid (BR) signaling regulates plant growth and development in concert with other signaling pathways. Although many genes have been identified that play a role in BR signaling, the biological and functional consequences of disrupting those key BR genes still require detailed investigation. RESULTS: Here we performed phenotypic and transcriptomic comparisons of A. thaliana lines carrying a loss-of-function mutation in BRI1 gene, bri1–5, that exhibits a dwarf phenotype and its three activation-tag suppressor lines that were able to partially revert the bri1–5 mutant phenotype to a WS2 phenotype, namely bri1–5/bri1–1D, bri1–5/brs1–1D, and bri1–5/bak1–1D. From the three investigated bri1–5 suppressors, bri1–5/bak1–1D was the most effective suppressor at the transcriptional level. All three bri1–5 suppressors showed altered expression of the genes in the abscisic acid (ABA signaling) pathway, indicating that ABA likely contributes to the partial recovery of the wild-type phenotype in these bri1–5 suppressors. Network analysis revealed crosstalk between BR and other phytohormone signaling pathways, suggesting that interference with one hormone signaling pathway affects other hormone signaling pathways. In addition, differential expression analysis suggested the existence of a strong negative feedback from BR signaling on BR biosynthesis and also predicted that BRS1, rather than being directly involved in signaling, might be responsible for providing an optimal environment for the interaction between BRI1 and its ligand. CONCLUSIONS: Our study provides insights into the molecular mechanisms and functions of key brassinosteroid (BR) signaling genes, especially BRS1. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07778-w. BioMed Central 2021-06-22 /pmc/articles/PMC8220701/ /pubmed/34157989 http://dx.doi.org/10.1186/s12864-021-07778-w 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
Seyed Rahmani, Razgar
Shi, Tao
Zhang, Dongzhi
Gou, Xiaoping
Yi, Jing
Miclotte, Giles
Marchal, Kathleen
Li, Jia
Genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes
title Genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes
title_full Genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes
title_fullStr Genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes
title_full_unstemmed Genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes
title_short Genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes
title_sort genome-wide expression and network analyses of mutants in key brassinosteroid signaling genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220701/
https://www.ncbi.nlm.nih.gov/pubmed/34157989
http://dx.doi.org/10.1186/s12864-021-07778-w
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