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      Genome-Wide Study of YABBY Genes in Upland Cotton and Their Expression Patterns under Different Stresses

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          Abstract

          Members of the YABBY gene family, a small plant-specific family of genes, have been proposed to function in specifying abaxial cell fate. Although to date little has been learned about cotton YABBY genes, completion of the cotton genome enables a comprehensive genome-wide analysis of YABBY genes in cotton. Here, a total of 12, 12, and 23 YABBY genes were identified in Gossypium arboreum (2n = 26, A 2), G. raimondii (2n = 26, D 5), and G. hirsutum (2n = 4x = 52, [AD] t), respectively. Sequence analysis showed that the N-terminal zinc-finger and C-terminal YABBY domains in YABBY proteins are highly conserved among cotton, Arabidopsis, and rice. Eighty-five genes from eight sequenced species naturally clustered into five groups, and the YAB2-like group could be divided into three sub-groups, indicating that YABBYs are highly conserved among the examined species. Orthologs from the At and Dt sub-genomes (where “t” indicates tetraploid) showed good collinearity, indicating that YABBY loci are highly conserved between these two sub-genomes. Whole-genome duplication was the primary cause of upland cotton YABBY gene expansion, segmental duplication played important roles in YABBY gene expansion within the At and Dt sub-genomes, and the YAB5-like group was mainly generated by segmental duplication. The long-terminal repeat retroelements Copia and Gypsy were identified as major transposable elements accompanying the appearance of duplicated YABBY genes, suggesting that transposable element expansion might be involved in gene duplication. Selection pressure analyses using PAML revealed that relaxed purifying selection might be the main impetus during evolution of YABBY genes in the examined species. Furthermore, exon/intron pattern and motif analyses indicated that genes within the same group were significantly conserved between Arabidopsis and cotton. In addition, the expression patterns in different tissues suggest that YABBY proteins may play roles in ovule development because YABBYs are highly expressed in ovules. The expression pattern of YABBY genes showed that approximately half of the YABBYs were down-regulated under different stress treatments. Collectively, our results represent a comprehensive genome-wide study of the YABBY gene family, which should be helpful in further detailed studies on the gene function and evolution of YABBY genes in cotton.

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            Ancient polyploidization predating divergence of the cereals, and its consequences for comparative genomics.

            Integration of structural genomic data from a largely assembled rice genome sequence, with phylogenetic analysis of sequence samples for many other taxa, suggests that a polyploidization event occurred approximately 70 million years ago, before the divergence of the major cereals from one another but after the divergence of the Poales from the Liliales and Zingiberales. Ancient polyploidization and subsequent "diploidization" (loss) of many duplicated gene copies has thus shaped the genomes of all Poaceae cereal, forage, and biomass crops. The Poaceae appear to have evolved as separate lineages for approximately 50 million years, or two-thirds of the time since the duplication event. Chromosomes that are predicted to be homoeologs resulting from this ancient duplication event account for a disproportionate share of incongruent loci found by comparison of the rice sequence to a detailed sorghum sequence-tagged site-based genetic map. Differential gene loss during diploidization may have contributed many of these incongruities. Such predicted homoeologs also account for a disproportionate share of duplicated sorghum loci, further supporting the hypothesis that the polyploidization event was common to sorghum and rice. Comparative gene orders along paleo-homoeologous chromosomal segments provide a means to make phylogenetic inferences about chromosome structural rearrangements that differentiate among the grasses. Superimposition of the timing of major duplication events on taxonomic relationships leads to improved understanding of comparative gene orders, enhancing the value of data from botanical models for crop improvement and for further exploration of genomic biodiversity. Additional ancient duplication events probably remain to be discovered in other angiosperm lineages.
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              Gene duplication and evolutionary novelty in plants.

              Duplication is a prominent feature of plant genomic architecture. This has led many researchers to speculate that gene duplication may have played an important role in the evolution of phenotypic novelty within plants. Until recently, however, it was difficult to make this connection. We are now beginning to understand how duplication has contributed to adaptive evolution in plants. In this review we introduce the sources of gene duplication and predictions of the various fates of duplicates. We also highlight several recent and pertinent examples from the literature. These examples demonstrate the importance of the functional characteristics of genes and the source of duplication in influencing evolutionary outcome.
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                Author and article information

                Contributors
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                07 February 2018
                2018
                : 9
                : 33
                Affiliations
                [1] 1Xinjiang Research Base, State Key Laboratory of Cotton Biology, Xinjiang Agricultural University , Urumqi, China
                [2] 2Institute of Cotton Research, Chinese Academy of Agricultural Sciences , Anyang, China
                Author notes

                Edited by: Edward Hollox, University of Leicester, United Kingdom

                Reviewed by: Dieter Hackenberg, University of Leicester, United Kingdom; Luciana Werneck Zuccherato, Universidade Federal de Minas Gerais, Brazil

                *Correspondence: Fuguang Li aylifug@ 123456163.com

                This article was submitted to Evolutionary and Population Genetics, a section of the journal Frontiers in Genetics

                †These authors have contributed equally to this work.

                Article
                10.3389/fgene.2018.00033
                5808293
                29467795
                6e392517-2f27-4be3-bb9f-01c3ad2d9f22
                Copyright © 2018 Yang, Gong, Wang, Jin, Xi, Li, Qin, Yang, Lu, Chen and Li.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 26 August 2017
                : 25 January 2018
                Page count
                Figures: 7, Tables: 2, Equations: 0, References: 84, Pages: 17, Words: 11275
                Funding
                Funded by: National Key R&D Program of China
                Award ID: 2016YFD0100500
                Categories
                Genetics
                Original Research

                Genetics
                polarity,gossypium hirsutum,abiotic stress,ovule,transcription factor,segmental duplication
                Genetics
                polarity, gossypium hirsutum, abiotic stress, ovule, transcription factor, segmental duplication

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