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      Root PRR7 Improves the Accuracy of the Shoot Circadian Clock through Nutrient Transport

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          Abstract

          The circadian clock allows plants to anticipate and adapt to periodic environmental changes. Organ- and tissue-specific properties of the circadian clock and shoot-to-root circadian signaling have been reported. While this long-distance signaling is thought to coordinate physiological functions across tissues, little is known about the feedback regulation of the root clock on the shoot clock in the hierarchical circadian network. Here, we show that the plant circadian clock conveys circadian information between shoots and roots through sucrose and K +. We also demonstrate that K + transport from roots suppresses the variance of period length in shoots and then improves the accuracy of the shoot circadian clock. Sucrose measurements and qPCR showed that root sucrose accumulation was regulated by the circadian clock. Furthermore, root circadian clock genes, including PSEUDO-RESPONSE REGULATOR7 ( PRR7), were regulated by sucrose, suggesting the involvement of sucrose from the shoot in the regulation of root clock gene expression. Therefore, we performed time-series measurements of xylem sap and micrografting experiments using prr7 mutants and showed that root PRR7 regulates K + transport and suppresses variance of period length in the shoot. Our modeling analysis supports the idea that root-to-shoot signaling contributes to the precision of the shoot circadian clock. We performed micrografting experiments that illustrated how root PRR7 plays key roles in maintaining the accuracy of shoot circadian rhythms. We thus present a novel directional signaling pathway for circadian information from roots to shoots and propose that plants modulate physiological events in a timely manner through various timekeeping mechanisms.

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          Orchestrated Transcription of Key Pathways in Arabidopsis by the Circadian Clock

          Like most organisms, plants have endogenous biological clocks that coordinate internal events with the external environment. We used high-density oligonucleotide microarrays to examine gene expression in Arabidopsis and found that 6% of the more than 8000 genes on the array exhibited circadian changes in steady-state messenger RNA levels. Clusters of circadian-regulated genes were found in pathways involved in plant responses to light and other key metabolic pathways. Computational analysis of cycling genes allowed the identification of a highly conserved promoter motif that we found to be required for circadian control of gene expression. Our study presents a comprehensive view of the temporal compartmentalization of physiological pathways by the circadian clock in a eukaryote.
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            A central integrator of transcription networks in plant stress and energy signalling.

            Photosynthetic plants are the principal solar energy converter sustaining life on Earth. Despite its fundamental importance, little is known about how plants sense and adapt to darkness in the daily light-dark cycle, or how they adapt to unpredictable environmental stresses that compromise photosynthesis and respiration and deplete energy supplies. Current models emphasize diverse stress perception and signalling mechanisms. Using a combination of cellular and systems screens, we show here that the evolutionarily conserved Arabidopsis thaliana protein kinases, KIN10 and KIN11 (also known as AKIN10/At3g01090 and AKIN11/At3g29160, respectively), control convergent reprogramming of transcription in response to seemingly unrelated darkness, sugar and stress conditions. Sensing and signalling deprivation of sugar and energy, KIN10 targets a remarkably broad array of genes that orchestrate transcription networks, promote catabolism and suppress anabolism. Specific bZIP transcription factors partially mediate primary KIN10 signalling. Transgenic KIN10 overexpression confers enhanced starvation tolerance and lifespan extension, and alters architecture and developmental transitions. Significantly, double kin10 kin11 deficiency abrogates the transcriptional switch in darkness and stress signalling, and impairs starch mobilization at night and growth. These studies uncover surprisingly pivotal roles of KIN10/11 in linking stress, sugar and developmental signals to globally regulate plant metabolism, energy balance, growth and survival. In contrast to the prevailing view that sucrose activates plant SnRK1s (Snf1-related protein kinases), our functional analyses of Arabidopsis KIN10/11 provide compelling evidence that SnRK1s are inactivated by sugars and share central roles with the orthologous yeast Snf1 and mammalian AMPK in energy signalling.
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              Plant circadian clocks increase photosynthesis, growth, survival, and competitive advantage.

              Circadian clocks are believed to confer an advantage to plants, but the nature of that advantage has been unknown. We show that a substantial photosynthetic advantage is conferred by correct matching of the circadian clock period with that of the external light-dark cycle. In wild type and in long- and short-circadian period mutants of Arabidopsis thaliana, plants with a clock period matched to the environment contain more chlorophyll, fix more carbon, grow faster, and survive better than plants with circadian periods differing from their environment. This explains why plants gain advantage from circadian control.
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                Author and article information

                Contributors
                Journal
                Plant Cell Physiol
                Plant Cell Physiol
                pcp
                Plant and Cell Physiology
                Oxford University Press (UK )
                0032-0781
                1471-9053
                March 2023
                07 January 2023
                07 January 2023
                : 64
                : 3
                : 352-362
                Affiliations
                departmentDivision of Integrated Life Science, Graduate School of Biostudies, Kyoto University , Yoshida-Konoecho, Sakyo-ku, Kyoto, 606-8501 Japan
                departmentGraduate School of Science and Technology, Nara Institute of Science and Technology , 8916-5 Takayama-Cho, Ikoma, Nara, 630-0192 Japan
                departmentFaculty of Design, Kyushu University , 4-9-1 Shiobaru, Minami-ku, Fukuoka, 815-8540 Japan
                departmentDepartment of Biology, Graduate School of Sciences and Technology for Innovation, Yamaguchi University , 1677-1 Yoshida, Yamaguchi, 753-8512 Japan
                departmentGraduate School of Science and Technology, Nara Institute of Science and Technology , 8916-5 Takayama-Cho, Ikoma, Nara, 630-0192 Japan
                departmentGraduate School of Science and Technology, Nara Institute of Science and Technology , 8916-5 Takayama-Cho, Ikoma, Nara, 630-0192 Japan
                departmentGraduate School of Science and Technology, Nara Institute of Science and Technology , 8916-5 Takayama-Cho, Ikoma, Nara, 630-0192 Japan
                departmentGraduate School of Science and Technology, Nara Institute of Science and Technology , 8916-5 Takayama-Cho, Ikoma, Nara, 630-0192 Japan
                departmentDivision of Integrated Life Science, Graduate School of Biostudies, Kyoto University , Yoshida-Konoecho, Sakyo-ku, Kyoto, 606-8501 Japan
                departmentDepartment of Biology, Graduate School of Sciences and Technology for Innovation, Yamaguchi University , 1677-1 Yoshida, Yamaguchi, 753-8512 Japan
                departmentFaculty of Design, Kyushu University , 4-9-1 Shiobaru, Minami-ku, Fukuoka, 815-8540 Japan
                departmentGraduate School of Science and Technology, Nara Institute of Science and Technology , 8916-5 Takayama-Cho, Ikoma, Nara, 630-0192 Japan
                Author notes
                *Corresponding author: E-mail, endo@ 123456bs.naist.jp
                Author information
                https://orcid.org/0000-0002-1417-6096
                https://orcid.org/0000-0002-3616-1493
                https://orcid.org/0000-0003-2642-6758
                https://orcid.org/0000-0002-4621-9679
                Article
                pcad003
                10.1093/pcp/pcad003
                10016326
                36631969
                a70a6c1c-4305-4abe-8198-d960e3aea33d
                © The Author(s) 2023. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 November 2022
                : 30 December 2022
                : 06 January 2023
                : 03 January 2023
                : 15 February 2023
                Page count
                Pages: 11
                Funding
                Funded by: KAKENHI, DOI 10.13039/501100001691;
                Award ID: 15H05958, 16H01240, 17K19392, 18H04781 and 18H02461 to M.E.; 18H05474 to H.I.; 19K03663 and 22K03453 to F.M.; 22H04726 to A.T.; 22K15144 to S.Y. and 19J20421 to K.U.)
                Categories
                Rapid Paper
                AcademicSubjects/SCI01180

                Plant science & Botany
                circadian clock,mathematical model,micrografting,potassium,root-to-shoot signaling

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