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      Arabidopsis thaliana ambient temperature responsive lncRNAs

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          Abstract

          Background

          Long non-coding RNAs (lncRNAs) have emerged as new class of regulatory molecules in animals where they regulate gene expression at transcriptional and post-transcriptional level. Recent studies also identified lncRNAs in plant genomes, revealing a new level of transcriptional complexity in plants. Thousands of lncRNAs have been predicted in the Arabidopsis thaliana genome, but only a few have been studied in depth.

          Results

          Here we report the identification of Arabidopsis lncRNAs that are expressed during the vegetative stage of development in either the shoot apical meristem or in leaves. We found that hundreds of lncRNAs are expressed in these tissues, of which 50 show differential expression upon an increase in ambient temperature. One of these lncRNAs, FLINC, is down-regulated at higher ambient temperature and affects ambient temperature-mediated flowering in Arabidopsis.

          Conclusion

          A number of ambient temperature responsive lncRNAs were identified with potential roles in the regulation of temperature-dependent developmental changes, such as the transition from the vegetative to the reproductive (flowering) phase. The challenge for the future is to characterize the biological function and molecular mode of action of the large number of ambient temperature-regulated lncRNAs that have been identified in this study.

          Electronic supplementary material

          The online version of this article (10.1186/s12870-018-1362-x) contains supplementary material, which is available to authorized users.

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          Most cited references34

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          Phytochromes function as thermosensors in Arabidopsis.

          Plants are responsive to temperature, and some species can distinguish differences of 1°C. In Arabidopsis, warmer temperature accelerates flowering and increases elongation growth (thermomorphogenesis). However, the mechanisms of temperature perception are largely unknown. We describe a major thermosensory role for the phytochromes (red light receptors) during the night. Phytochrome null plants display a constitutive warm-temperature response, and consistent with this, we show in this background that the warm-temperature transcriptome becomes derepressed at low temperatures. We found that phytochrome B (phyB) directly associates with the promoters of key target genes in a temperature-dependent manner. The rate of phyB inactivation is proportional to temperature in the dark, enabling phytochromes to function as thermal timers that integrate temperature information over the course of the night.
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            Phytochrome B integrates light and temperature signals in Arabidopsis

            Ambient temperature regulates many aspects of plant growth and development, but its sensors are unknown. Here, we demonstrate that the phytochrome B (phyB) photoreceptor participates in temperature perception through its temperature-dependent reversion from the active Pfr state to the inactive Pr state. Increased rates of thermal reversion upon exposing Arabidopsis seedlings to warm environments reduce both the abundance of the biologically active Pfr-Pfr dimer pool of phyB and the size of the associated nuclear bodies, even in daylight. Mathematical analysis of stem growth for seedlings expressing wild-type phyB or thermally stable variants under various combinations of light and temperature revealed that phyB is physiologically responsive to both signals. We therefore propose that in addition to its photoreceptor functions, phyB is a temperature sensor in plants.
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              Molecular and genetic control of plant thermomorphogenesis.

              Temperature is a major factor governing the distribution and seasonal behaviour of plants. Being sessile, plants are highly responsive to small differences in temperature and adjust their growth and development accordingly. The suite of morphological and architectural changes induced by high ambient temperatures, below the heat-stress range, is collectively called thermomorphogenesis. Understanding the molecular genetic circuitries underlying thermomorphogenesis is particularly relevant in the context of climate change, as this knowledge will be key to rational breeding for thermo-tolerant crop varieties. Until recently, the fundamental mechanisms of temperature perception and signalling remained unknown. Our understanding of temperature signalling is now progressing, mainly by exploiting the model plant Arabidopsis thaliana. The transcription factor PHYTOCHROME INTERACTING FACTOR 4 (PIF4) has emerged as a critical player in regulating phytohormone levels and their activity. To control thermomorphogenesis, multiple regulatory circuits are in place to modulate PIF4 levels, activity and downstream mechanisms. Thermomorphogenesis is integrally governed by various light signalling pathways, the circadian clock, epigenetic mechanisms and chromatin-level regulation. In this Review, we summarize recent progress in the field and discuss how the emerging knowledge in Arabidopsis may be transferred to relevant crop systems.
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                Author and article information

                Contributors
                severing@mpipz.mpg.de
                luigi.faino@uniroma1.it
                surajjamge@gmail.com
                marco.busscher@wur.nl
                yang.zhang.2@kaust.edu.sa
                francesca.bellinazzo@gmail.com
                jacqueline.busscher@wur.nl
                fernandez@mpipz.mpg.de
                gerco.angenent@wur.nl
                richard.immink@wur.nl
                alice.pajoro@gmail.com
                Journal
                BMC Plant Biol
                BMC Plant Biol
                BMC Plant Biology
                BioMed Central (London )
                1471-2229
                13 July 2018
                13 July 2018
                2018
                : 18
                : 145
                Affiliations
                [1 ]ISNI 0000 0001 0660 6765, GRID grid.419498.9, Max Planck Institute for Plant Breeding Research, ; 50829 Köln, Germany
                [2 ]ISNI 0000 0001 0791 5666, GRID grid.4818.5, Laboratory of Phytopathology, , Wageningen University and Research, ; 6708PB Wageningen, The Netherlands
                [3 ]ISNI 0000 0001 0791 5666, GRID grid.4818.5, Laboratory of Molecular Biology, , Wageningen University and Research, ; 6708PB, Wageningen, The Netherlands
                [4 ]ISNI 0000 0001 0791 5666, GRID grid.4818.5, Bioscience, , Wageningen University and Research, ; 6708PB Wageningen, The Netherlands
                Author information
                http://orcid.org/0000-0002-6419-548X
                Article
                1362
                10.1186/s12870-018-1362-x
                6045843
                30005624
                af8cac6e-78c4-46bf-9bfd-fd8c670410cc
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

                History
                : 31 October 2017
                : 4 July 2018
                Funding
                Funded by: NWO
                Award ID: 849.13.005 for the project ERACAPS13.012, FLOWPLAST
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Plant science & Botany
                long non-coding rna (lncrna),ambient temperature response,flowering time,arabidopsis thaliana,flinc

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