Genome-Wide Identification and Characterization of WRKY Transcription Factors in Betula platyphylla Suk. and Their Responses to Abiotic Stresses

被引:4
|
作者
Yu, Jiajie [1 ]
Zhang, Xiang [1 ]
Cao, Jiayu [1 ]
Bai, Heming [1 ]
Wang, Ruiqi [1 ]
Wang, Chao [1 ]
Xu, Zhiru [1 ,2 ]
Li, Chunming [1 ]
Liu, Guanjun [1 ]
机构
[1] Northeast Forestry Univ, State Key Lab Tree Genet & Breeding, Harbin 150040, Peoples R China
[2] Northeast Forestry Univ, Coll Life Sci, Harbin 150040, Peoples R China
关键词
Betula platyphylla; WRKY transcription factor; bioinformatics analysis; expression pattern; ABA treatment; salt treatment; cold treatment; protein interaction; subcellular localization; GENE-EXPRESSION DATA; PLANT-RESPONSES; FAMILY; RESISTANCE; SALT; TOLERANCE; PATHOGEN; DEFENSE; BASAL; RICE;
D O I
10.3390/ijms241915000
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The WRKY transcription factor (TF) family is one the largest plant-specific transcription factor families. It has been proven to play significant roles in multiple plant biological processes, especially stress response. Although many WRKY TFs have been identified in various plant species, WRKYs in white birch (Betula platyphylla Suk.) remain to be studied. Here, we identified a total of 68 BpWRKYs, which could be classified into four main groups. The basic physiochemical properties of these TFs were analyzed using bioinformatics tools, including molecular weight, isoelectric point, chromosome location, and predicted subcellular localization. Most BpWRKYs were predicted to be located in the nucleus. Synteny analysis found 17 syntenic gene pairs among BpWRKYs and 52 syntenic gene pairs between BpWRKYs and AtWRKYs. The cis-acting elements in the promoters of BpWRKYs could be enriched in multiple plant biological processes, including stress response, hormone response, growth and development, and binding sites. Tissue-specific expression analysis using qRT-PCR showed that most BpWRKYs exhibited highest expression levels in the root. After ABA, salt (NaCl), or cold treatment, different BpWRKYs showed different expression patterns at different treatment times. Furthermore, the results of the Y2H assay proved the interaction between BpWRKY17 and a cold-responsive TF, BpCBF7. By transient expression assay, BpWRKY17 and BpWRKY67 were localized in the nucleus, consistent with the previous prediction. Our study hopes to shed light for research on WRKY TFs and plant stress response.
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页数:18
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