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      Genetic control of flowering time in woody plants: Roses as an emerging model

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          Abstract

          Genetic control of the timing of flowering in woody plants is complex and has yet to be adequately investigated due to their long life-cycle and difficulties in genetic modification. Studies in Populus, one of the best woody plant models, have revealed a highly conserved genetic network for flowering timing in annuals. However, traits like continuous flowering cannot be addressed with Populus. Roses and strawberries have relatively small, diploid genomes and feature enormous natural variation. With the development of new genetic populations and genomic tools, roses and strawberries have become good models for studying the molecular mechanisms underpinning the regulation of flowering in woody plants. Here, we review findings on the molecular and genetic factors controlling continuous flowering in roses and woodland strawberries. Natural variation at TFL1 orthologous genes in both roses and strawberries seems be the key plausible factor that regulates continuous flowering. However, recent efforts suggest that a two-recessive-loci model may explain the controlling of continuous flowering in roses. We propose that epigenetic factors, including non-coding RNAs or chromatin-related factors, might also play a role. Insights into the genetic control of flowering time variation in roses should benefit the development of new germplasm for woody crops and shed light on the molecular genetic bases for the production and maintenance of plant biodiversity.

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          FLOWERING LOCUS C encodes a novel MADS domain protein that acts as a repressor of flowering.

          Winter-annual ecotypes of Arabidopsis are relatively late flowering, unless the flowering of these ecotypes is promoted by exposure to cold (vernalization). This vernalization-suppressible, late-flowering phenotype results from the presence of dominant, late-flowering alleles at two loci, FRIGIDA (FRI) and FLOWERING LOCUS C (FLC). In this study, we report that flc null mutations result in early flowering, demonstrating that the role of active FLC alleles is to repress flowering. FLC was isolated by positional cloning and found to encode a novel MADS domain protein. The levels of FLC mRNA are regulated positively by FRI and negatively by LUMINIDEPENDENS. FLC is also negatively regulated by vernalization. Overexpression of FLC from a heterologous promoter is sufficient to delay flowering in the absence of an active FRI allele. We propose that the level of FLC activity acts through a rheostat-like mechanism to control flowering time in Arabidopsis and that modulation of FLC expression is a component of the vernalization response.
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            Molecular analysis of FRIGIDA, a major determinant of natural variation in Arabidopsis flowering time.

            Vernalization, the acceleration of flowering by a long period of cold temperature, ensures that many plants overwinter vegetatively and flower in spring. In Arabidopsis, allelic variation at the FRIGIDA (FRI) locus is a major determinant of natural variation in flowering time. Dominant alleles of FRI confer late flowering, which is reversed to earliness by vernalization. We cloned FRI and analyzed the molecular basis of the allelic variation. Most of the early-flowering ecotypes analyzed carry FRI alleles containing one of two different deletions that disrupt the open reading frame. Loss-of-function mutations at FRI have thus provided the basis for the evolution of many early-flowering ecotypes.
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              SHOREmap: simultaneous mapping and mutation identification by deep sequencing.

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                Author and article information

                Contributors
                Journal
                Plant Divers
                Plant Divers
                Plant Diversity
                KeAi Publishing
                2096-2703
                2468-2659
                03 February 2017
                April 2017
                03 February 2017
                : 39
                : 2
                : 104-110
                Affiliations
                [a ]Group of Plant Molecular Genetics and Adaptation, Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences. Lanhei Road 132, Heilongtan, Kunming 650201, Yunnan Province, PR China
                [b ]Second High School, Rongcheng 264309, Shandong Province, PR China
                Author notes
                []Corresponding author. hujinyong@ 123456mail.kib.ac.cn
                Article
                S2468-2659(16)30076-2
                10.1016/j.pld.2017.01.004
                6112279
                8bcdbb1e-bad5-4677-8c54-aae80b3a2157
                © 2017 Kunming Institute of Botany, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 4 August 2016
                : 25 January 2017
                : 25 January 2017
                Categories
                Article

                rose,continuous flowering,model woody plant,genetics,bulk-segregation analysis,genome-wide prediction

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