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Interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs

BACKGROUND: The circadian clock drives endogenous 24-h rhythms that allow organisms to adapt and prepare for predictable and repeated changes in their environment throughout the day-night (diurnal) cycle. Many components of the circadian clock in Arabidopsis thaliana have been functionally character...

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Autores principales: Lai, Xianjun, Bendix, Claire, Yan, Lang, Zhang, Yang, Schnable, James C., Harmon, Frank G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315539/
https://www.ncbi.nlm.nih.gov/pubmed/32586356
http://dx.doi.org/10.1186/s12864-020-06824-3
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author Lai, Xianjun
Bendix, Claire
Yan, Lang
Zhang, Yang
Schnable, James C.
Harmon, Frank G.
author_facet Lai, Xianjun
Bendix, Claire
Yan, Lang
Zhang, Yang
Schnable, James C.
Harmon, Frank G.
author_sort Lai, Xianjun
collection PubMed
description BACKGROUND: The circadian clock drives endogenous 24-h rhythms that allow organisms to adapt and prepare for predictable and repeated changes in their environment throughout the day-night (diurnal) cycle. Many components of the circadian clock in Arabidopsis thaliana have been functionally characterized, but comparatively little is known about circadian clocks in grass species including major crops like maize and sorghum. RESULTS: Comparative research based on protein homology and diurnal gene expression patterns suggests the function of some predicted clock components in grasses is conserved with their Arabidopsis counterparts, while others have diverged in function. Our analysis of diurnal gene expression in three panicoid grasses sorghum, maize, and foxtail millet revealed conserved and divergent evolution of expression for core circadian clock genes and for the overall transcriptome. We find that several classes of core circadian clock genes in these grasses differ in copy number compared to Arabidopsis, but mostly exhibit conservation of both protein sequence and diurnal expression pattern with the notable exception of maize paralogous genes. We predict conserved cis-regulatory motifs shared between maize, sorghum, and foxtail millet through identification of diurnal co-expression clusters for a subset of 27,196 orthologous syntenic genes. In this analysis, a Cochran–Mantel–Haenszel based method to control for background variation identified significant enrichment for both expected and novel 6–8 nucleotide motifs in the promoter regions of genes with shared diurnal regulation predicted to function in common physiological activities. CONCLUSIONS: This study illustrates the divergence and conservation of circadian clocks and diurnal regulatory networks across syntenic orthologous genes in panacoid grass species. Further, conserved local regulatory sequences contribute to the architecture of these diurnal regulatory networks that produce conserved patterns of diurnal gene expression.
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spelling pubmed-73155392020-06-25 Interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs Lai, Xianjun Bendix, Claire Yan, Lang Zhang, Yang Schnable, James C. Harmon, Frank G. BMC Genomics Research Article BACKGROUND: The circadian clock drives endogenous 24-h rhythms that allow organisms to adapt and prepare for predictable and repeated changes in their environment throughout the day-night (diurnal) cycle. Many components of the circadian clock in Arabidopsis thaliana have been functionally characterized, but comparatively little is known about circadian clocks in grass species including major crops like maize and sorghum. RESULTS: Comparative research based on protein homology and diurnal gene expression patterns suggests the function of some predicted clock components in grasses is conserved with their Arabidopsis counterparts, while others have diverged in function. Our analysis of diurnal gene expression in three panicoid grasses sorghum, maize, and foxtail millet revealed conserved and divergent evolution of expression for core circadian clock genes and for the overall transcriptome. We find that several classes of core circadian clock genes in these grasses differ in copy number compared to Arabidopsis, but mostly exhibit conservation of both protein sequence and diurnal expression pattern with the notable exception of maize paralogous genes. We predict conserved cis-regulatory motifs shared between maize, sorghum, and foxtail millet through identification of diurnal co-expression clusters for a subset of 27,196 orthologous syntenic genes. In this analysis, a Cochran–Mantel–Haenszel based method to control for background variation identified significant enrichment for both expected and novel 6–8 nucleotide motifs in the promoter regions of genes with shared diurnal regulation predicted to function in common physiological activities. CONCLUSIONS: This study illustrates the divergence and conservation of circadian clocks and diurnal regulatory networks across syntenic orthologous genes in panacoid grass species. Further, conserved local regulatory sequences contribute to the architecture of these diurnal regulatory networks that produce conserved patterns of diurnal gene expression. BioMed Central 2020-06-25 /pmc/articles/PMC7315539/ /pubmed/32586356 http://dx.doi.org/10.1186/s12864-020-06824-3 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
Lai, Xianjun
Bendix, Claire
Yan, Lang
Zhang, Yang
Schnable, James C.
Harmon, Frank G.
Interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs
title Interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs
title_full Interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs
title_fullStr Interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs
title_full_unstemmed Interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs
title_short Interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs
title_sort interspecific analysis of diurnal gene regulation in panicoid grasses identifies known and novel regulatory motifs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7315539/
https://www.ncbi.nlm.nih.gov/pubmed/32586356
http://dx.doi.org/10.1186/s12864-020-06824-3
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