茶树CsMAPKK3基因克隆及表达分析

Cloning and expression analysis of CsMAPKK3 gene in tea plant

  • 摘要: 【目的】克隆茶树CsMAPKK3基因,并进行表达分析,为探究CsMAPKK3基因的生物学功能及其抗逆分子机制提供理论支持。【方法】以铁观音为材料,采用RT-PCR克隆其CsMAPKK3基因的全长cDNA序列,对其进行生物信息学分析,并采用实时荧光定量PCR(qRT-PCR)检测其在不同组织及逆境胁迫下的表达情况。【结果】克隆获得的CsMAPKK3基因(GenBank登录号:AUD40506.1)cDNA序列全长1941 bp,包含完整开放阅读框(ORF),长度为1557 bp,编码518个氨基酸残基,蛋白相对分子量为57.52 kD,理论等电点(pI)为5.39,为无跨膜螺旋结构和信号肽的不稳定蛋白,含有多个磷酸化位点,定位于细胞质和细胞核中,属于PKc类型的MAPKK,且具有SPS1、S_TKc等催化结构域,以及D(I/L/V)K激活域和S/T-X3-5-S/T保守域,与中华猕猴桃PSS35243.1亲缘关系最近,且与拟南芥B亚家族聚为一类。CsMAPKK3基因起始密码子上游1714 bp的启动子区序列含有光响应、逆境响应、植物激素和厌氧诱导等相关的顺式作用元件。CsMAPKK3基因在根、茎、叶、花和果中均有表达,其中在茎和果的表达量较高,显著高于在花中的表达量(P<0.05),但与根和叶中的表达量均无显著差异(P>0.05)。低温胁迫抑制CsMAPKK3基因表达,而脱落酸(ABA)、高盐和干旱胁迫均能诱导CsMAPKK3基因上调表达。【结论】CsMAPKK3基因表达具有组织表达特异性,且参与茶树ABA、高盐、低温和干旱胁迫响应等逆境胁迫的分子调控。

     

    Abstract: 【Objective】The CsMAPKK3 gene of tea tree was cloned and its expression was analyzed to provide theoretical support for clarifying the biological function of tea plant CsMAPKK3 gene and revealing its role in tea plant's stress resistance.【Method】In this study, the full-length cDNA of MAPKK3 gene were cloned using RT-PCR from Tieguanyin tea plant. Then, the bioinformatics characteristics and functions of CsMAPKK3 gene were predicted, and its expression patterns in various tissues and under different stress treatments were investigated using real-time fluorescence quantitative PCR.【Result】The full-length cDNA of CsMAPKK3 was 1941 bp, with a 1557 bp open reading frame(ORF), encoding 518 amino acids, and submitted to the GenBank with accession number of AUD40506.1. The molecular weight of CsMAPKK3 protein was 57.52 kD, and the theoretical isoelectric point(pI) was 5.39. The amino acid sequence prediction showed that it was an unstable protein without transmembrane helix structure and signal peptide, and contained multiple phosphorylation sites. CsMAPKK3 protein, located in cytoplasm and nucleus, belonged to PKC type MAPKK, and had catalytic domains such as SPS1, S_TKC, D(I/L/V) K activation domain and S/T-X3-5-S/T conserved domain. It had close relationship with Chinese kiwifruit(PSS35243.1), and was clustered in a class with Arabidopsis B subfamily in phylogenetic tree. Additionally, promoter sequence analysis showed that the 1714 bp promoter region in the initiation codon upstream of CsMAPKK3 contained several cis-acting elements related to light response, stress response, plant hormones, and anaerobic induction. Real time quantitative PCR analysis showed that CsMAPKK3 was expressed in roots, stems, leaves, flowers and fruits, and the expression level was higher in stems and fruits, which was significantly higher than that in flowers(P<0.05), but had no significant difference with that in roots and leaves(P>0.05). The expression of CsMAPKK3 was down-regulated by cold stress, but up-regulated by abscisic acid(ABA), salt and drought treatments.【Conclusion】The expression of CsMAPKK3 is tissue-specific, and it is involved in the tea plant response to ABA, high salt, low temperature and drought stresses.

     

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