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毛果杨中PHD指蛋白家族的全基因组鉴定、分类及表达分析

Genome-wide identification, classification and expression analysis of the PHD-finger protein family in Populus trichocarpa.

作者信息

Wu Shengnan, Wu Min, Dong Qing, Jiang Haiyang, Cai Ronghao, Xiang Yan

机构信息

Laboratory of Modern Biotechnology, School of Forestry and Landscape Architecture, Anhui Agricultural University, Hefei, China; Key Laboratory of Biomass Improvement and Conversion of Anhui Province, China.

Laboratory of Modern Biotechnology, School of Forestry and Landscape Architecture, Anhui Agricultural University, Hefei, China.

出版信息

Gene. 2016 Jan 1;575(1):75-89. doi: 10.1016/j.gene.2015.08.042. Epub 2015 Aug 24.

Abstract

The plant homeobox domain (PHD) proteins are widespread in eukaryotes, and play important roles in regulating chromatin and transcription. Comprehensive analyses of PHD-finger proteins have been performed in animals, but few plant PHD-finger proteins involved in growth and development have been characterized functionally. In this study, we conducted a genome-wide survey of PHD-finger proteins in Populus trichocarpa by describing the phylogenetic relationship, gene structure, and chromosomal location and microarray analyses of each predicted PHD-finger family member. We identified 73 PHD-finger genes (PtPHD1-73) and classified them into eleven subfamilies (A-K) by phylogenetic analysis. Seventy-two of the 73 genes were unevenly distributed on all 19 chromosomes, with seven segmental duplication events. Analysis of the Ka (non-synonymous substitution rate)/Ks (synonymous substitution rate) ratios suggested that the duplicated genes of the PHD-finger family mainly underwent purifying selection with restrictive functional divergence after the duplication events. Expression profiles analysis indicated that 67 PHD-finger genes were differentially expressed in various tissues. Quantitative real-time RT-PCR (qRT-PCR) analyses of nine selected PtPHD genes under high salinity, drought and cold stresses were also performed to explore their stress-related expression patterns. The results of this study provide a thorough overview of poplar PHD-finger proteins and will be valuable for further functional research of poplar PHD-finger genes to unravel their biological roles.

摘要

植物同源异型框结构域(PHD)蛋白广泛存在于真核生物中,在调节染色质和转录过程中发挥重要作用。在动物中已对PHD指蛋白进行了全面分析,但在植物中,很少有参与生长发育的PHD指蛋白得到功能鉴定。在本研究中,我们通过描述毛果杨中每个预测的PHD指家族成员的系统发育关系、基因结构、染色体定位和微阵列分析,对PHD指蛋白进行了全基因组调查。我们鉴定出73个PHD指基因(PtPHD1 - 73),并通过系统发育分析将它们分为11个亚家族(A - K)。73个基因中的72个不均匀地分布在所有19条染色体上,存在7个片段重复事件。对Ka(非同义替换率)/Ks(同义替换率)比值的分析表明,PHD指家族的重复基因在重复事件后主要经历了纯化选择,功能分歧受到限制。表达谱分析表明,67个PHD指基因在不同组织中差异表达。还对9个选定的PtPHD基因在高盐、干旱和寒冷胁迫下进行了定量实时RT-PCR(qRT-PCR)分析,以探索它们与胁迫相关的表达模式。本研究结果全面概述了杨树PHD指蛋白,对于进一步开展杨树PHD指基因的功能研究以揭示其生物学作用具有重要价值。

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