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Genome-wide characterization of the abscisic acid-, stress- and ripening-induced (ASR) gene family in wheat (Triticum aestivum L.)

文献类型： 外文期刊

作者： Li, Huawei 1 ; Guan, Haiying 2 ; Zhuo, Qicui 1 ; Wang, Zongshuai 1 ; Li, Shengdong 1 ; Si, Jisheng 1 ; Zhang, Bin 1 ; Fen 1 ;

作者机构： 1.Shandong Acad Agr Sci, Crop Res Inst, 202 Gongyebei Rd, Jinan 250100, Peoples R China

2.Shandong Acad Agr Sci, Key Lab Biol & Genet Improvement Maize Northern Y, Natl Engn Lab Wheat & Maize, Maize Res Inst,Minist Agr, Jinan 250100, Shandong, Peoples R China

3.Jinan Yongfeng Seed Ind Co Ltd, 3620 Pingannan Rd, Jinan 250100, Peoples R China

关键词： Abscisic acid-; stress-; and ripening-induced (ASR); Genome-wide; Tandem and segmental duplication; Phylogenetic analyses; Gene structure; Salt

期刊名称：BIOLOGICAL RESEARCH （ 影响因子：5.612； 五年影响因子：4.781 ）

ISSN： 0716-9760

年卷期： 2020 年 53 卷 1 期

页码：

收录情况： SCI

摘要： Background Abscisic acid-, stress-, and ripening-induced (ASR) genes are a class of plant specific transcription factors (TFs), which play important roles in plant development, growth and abiotic stress responses. The wheat ASRs have not been described in genome-wide yet. Methods We predicted the transmembrane regions and subcellular localization using the TMHMM server, and Plant-mPLoc server and CELLO v2.5, respectively. Then the phylogeny tree was built by MEGA7. The exon-intron structures, conserved motifs and TFs binding sites were analyzed by GSDS, MEME program and PlantRegMap, respectively. Results In wheat, 33ASR genes were identified through a genome-wide survey and classified into six groups. Phylogenetic analyses revealed that the TaASR proteins in the same group tightly clustered together, compared with those from other species. Duplication analysis indicated that the TaASR gene family has expanded mainly through tandem and segmental duplication events. Similar gene structures and conserved protein motifs of TaASRs in wheat were identified in the same groups. ASR genes contained various TF binding cites associated with the stress responses in the promoter region. Gene expression was generally associated with the expected group-specific expression pattern in five tissues, including grain, leaf, root, spike and stem, indicating the broad conservation of ASR genes function during wheat evolution. The qRT-PCR analysis revealed that several ASRs were up-regulated in response to NaCl and PEG stress. Conclusion We identified ASR genes in wheat and found that gene duplication events are the main driving force for ASR gene evolution in wheat. The expression of wheat ASR genes was modulated in responses to multiple abiotic stresses, including drought/osmotic and salt stress. The results provided important information for further identifications of the functions of wheat ASR genes and candidate genes for high abiotic stress tolerant wheat breeding.

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