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毛果杨中DREB转录因子亚家族的基因结构、分类及表达模式

Gene structures, classification, and expression models of the DREB transcription factor subfamily in Populus trichocarpa.

作者信息

Chen Yunlin, Yang Jingli, Wang Zhanchao, Zhang Haizhen, Mao Xuliang, Li Chenghao

机构信息

State Key Laboratory of Forest Genetics and Tree Breeding, Northeast Forestry University, 26 Hexing Road, Harbin 150040, China.

出版信息

ScientificWorldJournal. 2013 Nov 13;2013:954640. doi: 10.1155/2013/954640. eCollection 2013.

Abstract

We identified 75 dehydration-responsive element-binding (DREB) protein genes in Populus trichocarpa. We analyzed gene structures, phylogenies, domain duplications, genome localizations, and expression profiles. The phylogenic construction suggests that the PtrDREB gene subfamily can be classified broadly into six subtypes (DREB A-1 to A-6) in Populus. The chromosomal localizations of the PtrDREB genes indicated 18 segmental duplication events involving 36 genes and six redundant PtrDREB genes were involved in tandem duplication events. There were fewer introns in the PtrDREB subfamily. The motif composition of PtrDREB was highly conserved in the same subtype. We investigated expression profiles of this gene subfamily from different tissues and/or developmental stages. Sixteen genes present in the digital expression analysis had high levels of transcript accumulation. The microarray results suggest that 18 genes were upregulated. We further examined the stress responsiveness of 15 genes by qRT-PCR. A digital northern analysis showed that the PtrDREB17, 18, and 32 genes were highly induced in leaves under cold stress, and the same expression trends were shown by qRT-PCR. Taken together, these observations may lay the foundation for future functional analyses to unravel the biological roles of Populus' DREB genes.

摘要

我们在毛果杨中鉴定出75个脱水响应元件结合(DREB)蛋白基因。我们分析了基因结构、系统发育、结构域重复、基因组定位和表达谱。系统发育构建表明,PtrDREB基因亚家族在杨树中可大致分为六个亚型(DREB A-1至A-6)。PtrDREB基因的染色体定位表明有18个片段重复事件涉及36个基因,并且有6个冗余的PtrDREB基因参与串联重复事件。PtrDREB亚家族中的内含子较少。PtrDREB的基序组成在同一亚型中高度保守。我们研究了该基因亚家族在不同组织和/或发育阶段的表达谱。数字表达分析中存在的16个基因具有高水平的转录本积累。微阵列结果表明有18个基因上调。我们通过qRT-PCR进一步检测了15个基因的胁迫响应性。数字Northern分析表明,PtrDREB17、18和32基因在冷胁迫下的叶片中被高度诱导,qRT-PCR也显示出相同的表达趋势。综上所述,这些观察结果可能为未来的功能分析奠定基础,以揭示杨树DREB基因的生物学作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3406/3845248/f55fa8aeb138/TSWJ2013-954640.001.jpg

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