首页|杜仲BR受体蛋白基因EuBRI1克隆及生物信息学分析

杜仲BR受体蛋白基因EuBRI1克隆及生物信息学分析

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为解析杜仲BR 相关基因功能,本研究通过前期构建的杜仲转录组数据库注释的信息,获得BRI1同源序列.设计特异性引物,以杜仲基因组DNA 及cDNA 为模板进行PCR 扩增克隆得到3 612 bp cDNA 序列,命名为EuBRI1.序列分析发现EuBRI1 是一个无内含子的完整开放阅读框,编码1 203 个氨基酸的蛋白.分析表明,EuBRI1 为稳定亲水性蛋白,相对分子质量为131.361 kD;理论等电点pI 为6.31;对其二级结构分析显示α-螺旋占31.50%,无规卷曲占55.94%,延伸链占12.55%,EuBRI1 含信号肽序列和跨膜结构以及 BRI1 家族激酶的保守结构域.进化树分析表明,EuBRI1 蛋白序列与醋栗番茄(Solanum pimpinellifolium) BRI1 进化上较接近,与橡胶树(Hevea brasiliensis) BRI1 相对等较远.研究结果为进一步阐明杜仲BR 相关基因的功能奠定基础.
Cloning and Bioinformatics Analysis of Brassinosteroid insensitive 1 Gene in Eucommia ulmoides
To analyze the function of Brassinosteroid relative genes in Eucommia ulmoides. The homologous sequence of BRI1 was found according to the annotation of Eucommia ulmoides transcriptase database constructed by our laboratory. The reference sequence of the gene was found by comparison with genome data. Specific primers were designed, and the 3 612 bp DNA sequence was obtained, which named EuBRI1. Sequence analysis revealed that EuBRI1 is a complete open reading frame without introns, encoding a protein of 1 203 amino acids. The EuBRI1 encoding protein has isoelect point (PI) of 6.31 and a calculated molecular weight about 131.361 kD, with transmembrane regions and signal peptitde has a Kinase conserved domain of BRI1 family. In the secondary structure, the percentage of alpha helix, β-extended, and random coil were 31.50%, 55.94%, 12.55%, respectively. The phylogenetic tree analysis indicates the level evelution of EuBRI1 is similarity with Solanum pimpinellifolium BRI1. We acquired valuable information which can be used to study the biological function of the EuBRI1 gene.

Eucommia ulmoidesEuBRI1Gene cloningBioinformatics analysis

刘明月、赵懿琛、赵德刚

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贵州大学农业生物工程研究院,生命科学学院,山地植物资源保护与种质创新省部共建教育部重点实验室,贵阳,550025

贵州大学茶学院,贵阳,550025

贵州省农业科学院,贵阳,550006

杜仲 EuBRI1 基因克隆 生物信息学分析

国家863计划"特色植物功能基因组学研究与应用"子项目%%

2013AA102605贵大人基合字201435号

2018

基因组学与应用生物学
广西大学

基因组学与应用生物学

CSTPCDCSCD北大核心
影响因子:1.108
ISSN:1674-568X
年,卷(期):2018.37(4)
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