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Evolutionary Insight into the Clock-Associated PRR5 Transcriptional Network of Flowering Plants

Circadian clocks regulate the daily timing of metabolic, physiological, and behavioral activities to adapt organisms to day-night cycles. In the model plant Arabidopsis thaliana, transcript-translational feedback loops (TTFL) constitute the circadian clock, which is conserved among flowering plants....

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Autores principales: Toda, Yosuke, Kudo, Toru, Kinoshita, Toshinori, Nakamichi, Norihito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393427/
https://www.ncbi.nlm.nih.gov/pubmed/30814643
http://dx.doi.org/10.1038/s41598-019-39720-2
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author Toda, Yosuke
Kudo, Toru
Kinoshita, Toshinori
Nakamichi, Norihito
author_facet Toda, Yosuke
Kudo, Toru
Kinoshita, Toshinori
Nakamichi, Norihito
author_sort Toda, Yosuke
collection PubMed
description Circadian clocks regulate the daily timing of metabolic, physiological, and behavioral activities to adapt organisms to day-night cycles. In the model plant Arabidopsis thaliana, transcript-translational feedback loops (TTFL) constitute the circadian clock, which is conserved among flowering plants. Arabidopsis TTFL directly regulates key genes in the clock-output pathways, whereas the pathways for clock-output control in other plants is largely unknown. Here, we propose that the transcriptional networks of clock-associated pseudo-response regulators (PRRs) are conserved among flowering plants. Most PRR genes from Arabidopsis, poplar, and rice encode potential transcriptional repressors. The PRR5-target-like gene group includes genes that encode key transcription factors for flowering time regulation, cell elongation, and chloroplast gene expression. The 5′-upstream regions of PRR5-target-like genes from poplar and rice tend to contain G-box-like elements that are potentially recognized by PRRs in vivo as has been shown in Arabidopsis. Expression of PRR5-target-like genes from poplar and rice tends to decrease when PRRs are expressed, possibly suggesting that the transcriptional network of PRRs is evolutionarily conserved in these plants.
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spelling pubmed-63934272019-03-01 Evolutionary Insight into the Clock-Associated PRR5 Transcriptional Network of Flowering Plants Toda, Yosuke Kudo, Toru Kinoshita, Toshinori Nakamichi, Norihito Sci Rep Article Circadian clocks regulate the daily timing of metabolic, physiological, and behavioral activities to adapt organisms to day-night cycles. In the model plant Arabidopsis thaliana, transcript-translational feedback loops (TTFL) constitute the circadian clock, which is conserved among flowering plants. Arabidopsis TTFL directly regulates key genes in the clock-output pathways, whereas the pathways for clock-output control in other plants is largely unknown. Here, we propose that the transcriptional networks of clock-associated pseudo-response regulators (PRRs) are conserved among flowering plants. Most PRR genes from Arabidopsis, poplar, and rice encode potential transcriptional repressors. The PRR5-target-like gene group includes genes that encode key transcription factors for flowering time regulation, cell elongation, and chloroplast gene expression. The 5′-upstream regions of PRR5-target-like genes from poplar and rice tend to contain G-box-like elements that are potentially recognized by PRRs in vivo as has been shown in Arabidopsis. Expression of PRR5-target-like genes from poplar and rice tends to decrease when PRRs are expressed, possibly suggesting that the transcriptional network of PRRs is evolutionarily conserved in these plants. Nature Publishing Group UK 2019-02-27 /pmc/articles/PMC6393427/ /pubmed/30814643 http://dx.doi.org/10.1038/s41598-019-39720-2 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Toda, Yosuke
Kudo, Toru
Kinoshita, Toshinori
Nakamichi, Norihito
Evolutionary Insight into the Clock-Associated PRR5 Transcriptional Network of Flowering Plants
title Evolutionary Insight into the Clock-Associated PRR5 Transcriptional Network of Flowering Plants
title_full Evolutionary Insight into the Clock-Associated PRR5 Transcriptional Network of Flowering Plants
title_fullStr Evolutionary Insight into the Clock-Associated PRR5 Transcriptional Network of Flowering Plants
title_full_unstemmed Evolutionary Insight into the Clock-Associated PRR5 Transcriptional Network of Flowering Plants
title_short Evolutionary Insight into the Clock-Associated PRR5 Transcriptional Network of Flowering Plants
title_sort evolutionary insight into the clock-associated prr5 transcriptional network of flowering plants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393427/
https://www.ncbi.nlm.nih.gov/pubmed/30814643
http://dx.doi.org/10.1038/s41598-019-39720-2
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