Abstract

BackgroundGRAS proteins belong to a plant transcription factor family that is involved with multifarious roles in plants. Although previous studies of this protein family have been reported for Arabidopsis, rice, Chinese cabbage and other species, investigation of expansion patterns and evolutionary rate on the basis of comparative genomics in different species remains inadequate.ResultsA total of 289 GRAS genes were identified in Arabidopsis, B. distachyon, rice, soybean, S. moellendorffii, and P. patens and were grouped into seven subfamilies, supported by the similarity of their exon–intron patterns and structural motifs. All of tandem duplicated genes were found in group II except one cluster of rice, indicating that tandem duplication greatly promoted the expansion of group II. Furthermore, segment duplications were mainly found in the soybean genome, whereas no single expansion pattern dominated in other plant species indicating that GRAS genes from these five species might be subject to a more complex evolutionary mechanism. Interestingly, branch-site model analyses of positive selection showed that a number of sites were positively selected under foreground branches I and V. These results strongly indicated that these groups were experiencing higher positive selection pressure. Meanwhile, the site-specific model revealed that the GRAS genes were under strong positive selection in P. patens. DIVERGE v2.0 was used to detect critical amino acid sites, and the results showed that the shifted evolutionary rate was mainly attributed to the functional divergence between the GRAS genes in the two groups. In addition, the results also demonstrated the expression divergence of the GRAS duplicated genes in the evolution. In short, the results above provide a solid foundation for further functional dissection of the GRAS gene superfamily.ConclusionsIn this work, differential expression, evolutionary rate, and expansion patterns of the GRAS gene family in the six species were predicted. Especially, tandem duplication events played an important role in expansion of group II. Together, these results contribute to further functional analysis and the molecular evolution of the GRAS gene superfamily.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-014-0373-5) contains supplementary material, which is available to authorized users.

Highlights

  • GRAS proteins belong to a plant transcription factor family that is involved with multifarious roles in plants

  • Genome-wide identification of GRAS gene family In silico analyses have predicted that 33, 44, 47, 106, 21, and 38 GRAS genes exist in Arabidopsis, B. distachyon, rice, soybean, S. moellendorffii, and P. patens, respectively (Additional files 1 and 2)

  • The present study showed that most identified segmentally duplicated genes in six species were retained by wholegenome duplication (WGD), which supported the results of Edger et al On the other hand, in terms of groups, group II (67 genes, 23.2%) was the largest clade within the total group of GRAS genes, and most of the deduced tandemly duplicated genes were found in that group

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Summary

Introduction

GRAS proteins belong to a plant transcription factor family that is involved with multifarious roles in plants. Transcriptional regulation of gene expression is the one of the most important regulatory mechanisms in plants. Transcription factors can be grouped into specific families on the basis of their shared structural characteristics. GRAS proteins belong to a plant family of transcription factors and are. ? 2014 Wu et al.; licensee BioMed Central. 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

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