刚毛柽柳ThGAI 基因克隆及表达分析
Gene Cloning and Expression Analysis of ThGAI from Tamarix hispida
通过对刚毛柽柳转录组分析,克隆获得了一条柽柳DELLA家族蛋白基因,命名为ThGAI。序列分析结果表明:ThGAI基因全长cDNA为2901bp,包括1980bp的开放阅读框(ORF),推测ThGAI基因编码659个氨基酸,编码蛋白相对分子质量为71.99kDa,等电点为5.58。通过生物信息学分析发现ThGAI基因编码蛋白具有DELLA蛋白特有的结构域;氨基酸多序列比对和系统进化树分析,ThGAI基因编码氨基酸序列与其他已知植物DELLA蛋白有较高的同源性,属于DELLA亚家族成员,并具有VHYNP结构域、POLY(S/T)结构域、核定位NLS、VHVID结构域、亮氨酸结构域以及GRAS结构域,并且与玉米ZmGAI亲缘性最近。实时荧光定量RT-PCR分析表明,ThGAI表达受NaCl和PEG诱导,暗示赤霉素(GA)可能参与了刚毛柽柳的非生物胁迫响应过程。
he ThGAI gene was successfully cloned from the transcrip cDNA library of Tamarix hispida . Sequence analysis indicated that is 2901bp in length, containing an open reading frame of 1980bp, encoding 659 amino acids. The estimated molecular weight and isoelectric point of the putative protein were 71.99 kDa and 5.58, respectively. Bioinformatics analysis indicated that the typical domains of DELLA protein were found in the protein encoded by ThGAI gene. Amino acid sequence alignment with other species and phylogenetic analysis indicates that the deduced amino acid sequence of ThGAI gene was highly homologous with those of DELLA protein from other plants,was the number of DELLA .They had the DELLA protein typical domains such as TVHYNP, POLY(S/T),NLS,VHIID and the conserved GRAS domain. They had the highest homology of with ZmGAI from Zea mays Linn. Quantitative real-time PCR assay revealed that the mRNA levels of ThGAI was significantly up-regulated under NaCl and PEG treatments, suggesting that GA may be involved in abiotic stress response of Tamarix hispida.
王超、张春蕊、张玉、张悦
分子生物学植物学
刚毛柽柳hGAI基因ELLA蛋白表达分析
amarix hispidahGAI geneELLA proteinexpression analysis
王超,张春蕊,张玉,张悦.刚毛柽柳ThGAI 基因克隆及表达分析[EB/OL].(2017-04-26)[2025-08-10].http://www.paper.edu.cn/releasepaper/content/201704-611.点此复制
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