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      Multi-level analysis of the interactions between REVOLUTA and MORE AXILLARY BRANCHES 2 in controlling plant development reveals parallel, independent and antagonistic functions

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          ABSTRACT

          Class III homeodomain leucine zipper (HD-ZIPIII) transcription factors play fundamental roles in controlling plant development. The known HD-ZIPIII target genes encode proteins involved in the production and dissipation of the auxin signal, HD-ZIPII transcription factors and components that feedback to regulate HD-ZIPIII expression or protein activity. Here, we have investigated the regulatory hierarchies of the control of MORE AXILLARY BRANCHES2 ( MAX2) by the HD-ZIPIII protein REVOLUTA (REV). We found that REV can interact with the promoter of MAX2. In agreement, rev10D gain-of-function mutants had increased levels of MAX2 expression, while rev loss-of-function mutants showed lower levels of MAX2 in some tissues. Like REV, MAX2 plays known roles in the control of plant architecture, photobiology and senescence, which prompted us to initiate a multi-level analysis of growth phenotypes of hd-zipIII, max2 and respective higher order mutants thereof. Our data suggest a complex relationship of synergistic and antagonistic activities between REV and MAX2; these interactions appear to depend on the developmental context and do not all involve the direct regulation of MAX2 by REV.

          Abstract

          Summary: A complex relationship of synergistic and antagonistic activities exists between REV and MAX2 that appear to depend on the developmental context and do not all involve the direct regulation of MAX2 by REV.

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          Most cited references55

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          A new mathematical model for relative quantification in real-time RT-PCR.

          M. Pfaffl (2001)
          Use of the real-time polymerase chain reaction (PCR) to amplify cDNA products reverse transcribed from mRNA is on the way to becoming a routine tool in molecular biology to study low abundance gene expression. Real-time PCR is easy to perform, provides the necessary accuracy and produces reliable as well as rapid quantification results. But accurate quantification of nucleic acids requires a reproducible methodology and an adequate mathematical model for data analysis. This study enters into the particular topics of the relative quantification in real-time RT-PCR of a target gene transcript in comparison to a reference gene transcript. Therefore, a new mathematical model is presented. The relative expression ratio is calculated only from the real-time PCR efficiencies and the crossing point deviation of an unknown sample versus a control. This model needs no calibration curve. Control levels were included in the model to standardise each reaction run with respect to RNA integrity, sample loading and inter-PCR variations. High accuracy and reproducibility (<2.5% variation) were reached in LightCycler PCR using the established mathematical model.
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            Strigolactone inhibition of shoot branching.

            A carotenoid-derived hormonal signal that inhibits shoot branching in plants has long escaped identification. Strigolactones are compounds thought to be derived from carotenoids and are known to trigger the germination of parasitic plant seeds and stimulate symbiotic fungi. Here we present evidence that carotenoid cleavage dioxygenase 8 shoot branching mutants of pea are strigolactone deficient and that strigolactone application restores the wild-type branching phenotype to ccd8 mutants. Moreover, we show that other branching mutants previously characterized as lacking a response to the branching inhibition signal also lack strigolactone response, and are not deficient in strigolactones. These responses are conserved in Arabidopsis. In agreement with the expected properties of the hormonal signal, exogenous strigolactone can be transported in shoots and act at low concentrations. We suggest that endogenous strigolactones or related compounds inhibit shoot branching in plants. Furthermore, ccd8 mutants demonstrate the diverse effects of strigolactones in shoot branching, mycorrhizal symbiosis and parasitic weed interaction.
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              Inhibition of shoot branching by new terpenoid plant hormones.

              Shoot branching is a major determinant of plant architecture and is highly regulated by endogenous and environmental cues. Two classes of hormones, auxin and cytokinin, have long been known to have an important involvement in controlling shoot branching. Previous studies using a series of mutants with enhanced shoot branching suggested the existence of a third class of hormone(s) that is derived from carotenoids, but its chemical identity has been unknown. Here we show that levels of strigolactones, a group of terpenoid lactones, are significantly reduced in some of the branching mutants. Furthermore, application of strigolactones inhibits shoot branching in these mutants. Strigolactones were previously found in root exudates acting as communication chemicals with parasitic weeds and symbiotic arbuscular mycorrhizal fungi. Thus, we propose that strigolactones act as a new hormone class-or their biosynthetic precursors-in regulating above-ground plant architecture, and also have a function in underground communication with other neighbouring organisms.
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                Author and article information

                Journal
                Development
                Development
                DEV
                develop
                Development (Cambridge, England)
                The Company of Biologists Ltd
                0950-1991
                1477-9129
                15 May 2020
                21 May 2020
                21 May 2020
                : 147
                : 10
                : dev183681
                Affiliations
                [1 ]Copenhagen Plant Science Centre, University of Copenhagen , Thorvaldsensvej 40, 1871 Frederiksberg C, Denmark
                [2 ]Department of Plant and Environmental Sciences, Faculty of Science, University of Copenhagen , Copenhagen, Denmark
                [3 ]Centre for Plant Molecular Biology (ZMBP), University of Tübingen , Auf der Morgenstelle 32, 72076 Tübingen, Germany
                [4 ]State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and National Center for Plant Gene Research , Beijing 100101, China
                [5 ]NovoCrops Center, PLEN, University of Copenhagen , Thorvaldsensvej 40, 1871 Frederiksberg C, Denmark
                Author notes
                [*]

                These authors contributed equally to this work

                []Author for correspondence ( wenkel@ 123456plen.ku.dk )

                Handling Editor: Ykä Helariutta

                Author information
                http://orcid.org/0000-0003-3031-2753
                http://orcid.org/0000-0002-4848-074X
                http://orcid.org/0000-0001-5609-3742
                http://orcid.org/0000-0003-1943-9577
                http://orcid.org/0000-0001-5764-9423
                Article
                DEV183681
                10.1242/dev.183681
                7325436
                32345745
                2d6fe9c6-4e38-47c9-b632-adb86734f3dc
                © 2020. Published by The Company of Biologists Ltd

                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 use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 9 August 2019
                : 19 April 2020
                Funding
                Funded by: University of Copenhagen, http://dx.doi.org/10.13039/501100001734;
                Funded by: Det Frie Forskningsråd, http://dx.doi.org/10.13039/501100004836;
                Award ID: DFF-6108-00091
                Funded by: Novo Nordisk Fonden, http://dx.doi.org/10.13039/501100009708;
                Award ID: NNF19OC005658
                Award ID: NNF18OC0034226
                Funded by: Deutsche Forschungsgemeinschaft, http://dx.doi.org/10.13039/501100001659;
                Award ID: SFB1101
                Funded by: National Natural Science Foundation of China, http://dx.doi.org/10.13039/501100001809;
                Award ID: 31872835
                Categories
                201
                Research Article

                Developmental biology
                shade avoidance,shoot branching,senescence,vascular development,hd-zipiii,arabidopsis

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