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茶树全基因组鉴定和 CsSnRK2 家族特征分析。

Genome-wide identification and characterization of the CsSnRK2 family in Camellia sinensis.

机构信息

College of Horticulture, Northwest A&F University, Yangling, 712100, Shaanxi, China.

College of Horticulture, Northwest A&F University, Yangling, 712100, Shaanxi, China.

出版信息

Plant Physiol Biochem. 2018 Nov;132:287-296. doi: 10.1016/j.plaphy.2018.09.021. Epub 2018 Sep 17.

DOI:10.1016/j.plaphy.2018.09.021
PMID:30245342
Abstract

The sucrose nonfermenting 1 (SNF1)-related protein kinase 2 (SnRK2) genes play central roles in plant stress signal transduction. In this study, 8 SnRK2 genes were identified from the tea plant genome database and named CsSnRK2.1-8. Phylogenetic analysis showed that the CsSnRK2 genes were classifiable into three groups, similar to those of Arabidopsis thaliana, Oryza sativa and maize. The coding sequences (CDSs) of all CsSnRK2s were separated by eight introns, and their exon-intron organizations exhibited high similarity to those of other plants. The fluorescence of GFP fused with CsSnRK2.3 was detected in only the cytoplasm, while the rest of the proteins showed GFP signal in both the nucleus and the cytoplasm. The results of the expression patterns of the CsSnRK2 genes showed that CsSnRK2s were differentially induced by salt, polyethylene glycol (PEG) and abscisic acid (ABA) stress. Interestingly, The expression of CsSnRK2.3 was inhibited by ABA, suggesting the complicated roles of CsSnRK2s in the ABA signal transduction pathway. Some CsSnRK2 gene pairs showed significant expression change correlations under stresses, indicating that CsSnRK2s might exhibit synergistic effects of signal regulation in response to various stresses. In summary, this comprehensive analysis will facilitate further studies of the SnRK2 family of Camellia sinensis and provide useful information for the functional validation of CsSnRK2s.

摘要

蔗糖非发酵 1(SNF1)相关蛋白激酶 2(SnRK2)基因在植物应激信号转导中发挥核心作用。本研究从茶树基因组数据库中鉴定出 8 个 SnRK2 基因,并将其命名为 CsSnRK2.1-8。系统进化分析表明,CsSnRK2 基因可分为三组,与拟南芥、水稻和玉米的相似。所有 CsSnRK2 的编码序列(CDS)都被 8 个内含子隔开,它们的外显子-内含子组织与其他植物非常相似。GFP 与 CsSnRK2.3 融合的荧光仅在细胞质中检测到,而其余蛋白质在核和细胞质中均显示 GFP 信号。CsSnRK2 基因表达模式的结果表明,CsSnRK2 基因对盐、聚乙二醇(PEG)和脱落酸(ABA)胁迫有不同的诱导作用。有趣的是,ABA 抑制 CsSnRK2.3 的表达,表明 CsSnRK2 在 ABA 信号转导途径中具有复杂的作用。一些 CsSnRK2 基因对在胁迫下表现出显著的表达变化相关性,表明 CsSnRK2 可能在应对各种胁迫时表现出协同的信号调控作用。综上所述,这项综合分析将有助于进一步研究茶树的 SnRK2 家族,并为 CsSnRK2 的功能验证提供有用的信息。

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