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      Functional Evolution in the Plant SQUAMOSA-PROMOTER BINDING PROTEIN-LIKE ( SPL) Gene Family

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          Abstract

          The SQUAMOSA-PROMOTER BINDING PROTEIN-LIKE ( SPL) family of transcription factors is functionally diverse, controlling a number of fundamental aspects of plant growth and development, including vegetative phase change, flowering time, branching, and leaf initiation rate. In natural plant populations, variation in flowering time and shoot architecture have major consequences for fitness. Likewise, in crop species, variation in branching and developmental rate impact biomass and yield. Thus, studies aimed at dissecting how the various functions are partitioned among different SPL genes in diverse plant lineages are key to providing insight into the genetic basis of local adaptation and have already garnered attention by crop breeders. Here we use phylogenetic reconstruction to reveal nine major SPL gene lineages, each of which is described in terms of function and diversification. To assess evidence for ancestral and derived functions within each SPL gene lineage, we use ancestral character state reconstructions. Our analyses suggest an emerging pattern of sub-functionalization, neo-functionalization, and possible convergent evolution following both ancient and recent gene duplication. Based on these analyses we suggest future avenues of research that may prove fruitful for elucidating the importance of SPL gene evolution in plant growth and development.

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          Most cited references76

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          Evolution by gene duplication: an update

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            Specific effects of microRNAs on the plant transcriptome.

            Most plant microRNAs (miRNAs) have perfect or near-perfect complementarity with their targets. This is consistent with their primary mode of action being cleavage of target mRNAs, similar to that induced by perfectly complementary small interfering RNAs (siRNAs). However, there are natural targets with up to five mismatches. Furthermore, artificial siRNAs can have substantial effects on so-called off-targets, to which they have only limited complementarity. By analyzing the transcriptome of plants overexpressing different miRNAs, we have deduced a set of empirical parameters for target recognition. Compared to artificial siRNAs, authentic plant miRNAs appear to have much higher specificity, which may reflect their coevolution with the remainder of the transcriptome. We also demonstrate that miR172, previously thought to act primarily by translational repression, can efficiently guide mRNA cleavage, although the effects on steady-state levels of target transcripts are obscured by strong feedback regulation. This finding unifies the view of plant miRNA action.
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              A naturally occurring epigenetic mutation in a gene encoding an SBP-box transcription factor inhibits tomato fruit ripening.

              A major component in the regulatory network controlling fruit ripening is likely to be the gene at the tomato Colorless non-ripening (Cnr) locus. The Cnr mutation results in colorless fruits with a substantial loss of cell-to-cell adhesion. The nature of the mutation and the identity of the Cnr gene were previously unknown. Using positional cloning and virus-induced gene silencing, here we demonstrate that an SBP-box (SQUAMOSA promoter binding protein-like) gene resides at the Cnr locus. Furthermore, the Cnr phenotype results from a spontaneous epigenetic change in the SBP-box promoter. The discovery that Cnr is an epimutation was unexpected, as very few spontaneous epimutations have been described in plants. This study demonstrates that an SBP-box gene is critical for normal ripening and highlights the likely importance of epialleles in plant development and the generation of natural variation.
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                Author and article information

                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                25 February 2013
                05 April 2013
                2013
                : 4
                : 80
                Affiliations
                [1] 1Plant Biology, The University of Vermont Burlington, VT, USA
                [2] 2Ecology and Evolutionary Biology, The University of Kansas Lawrence, KS, USA
                Author notes

                Edited by: Elena M. Kramer, Harvard University, USA

                Reviewed by: Elena M. Kramer, Harvard University, USA; Pablo D. Jenik, Franklin & Marshall College, USA

                *Correspondence: Jill C. Preston, Department of Plant Biology, The University of Vermont, 111 Jeffords Hall, 63 Carrigan Drive, Burlington, VT 05405, USA. e-mail: jill.preston@ 123456uvm.edu

                This article was submitted to Frontiers in Plant Evolution and Development, a specialty of Frontiers in Plant Science.

                Article
                10.3389/fpls.2013.00080
                3617394
                23577017
                e18d590e-6646-444b-83d5-754ed84f92bb
                Copyright © 2013 Preston and Hileman.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 12 February 2013
                : 19 March 2013
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 103, Pages: 13, Words: 10480
                Categories
                Plant Science
                Review Article

                Plant science & Botany
                spl genes,gene duplication,phase change,flowering time,branching architecture,developmental transitions

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