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张祥云

作品数:3 被引量:4H指数:1
供职机构:聊城大学生命科学学院更多>>
发文基金:国家自然科学基金山东省自然科学基金国家重点实验室开放基金更多>>
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Cloning and Phylogenetic Analysis of Ubiquitinconjugating Enzyme Gene TaUBC4 in Different Wheat Cultivars
2014年
[Objective] This study aimed to clone ubiquitin-conjugating enzyme gene TaUBC4 from different wheat cultivars and thus analyze their phylogenetic relationship.[Method] The UBC4 coding sequences were cloned through reverse transcription PCR (RT-PCR) from 21 wheat varieties.After sequencing,the UBC4 sequence in wheat cultivar Zhongguochun (GenBank accession No:M28059) was selected as the reference gene,to analyze the mutation frequency and evolutionary distance in the CDSs and corresponding amino acid sequences of the different wheat cultivars.Moreover,the phylogenetic tree based on the amino acid sequences of these TaUBC4 genes were constructed,involving the homologous sequences of TaUBC4 in eight other monocots.[Result] TaUBC4 sequence was highly conserved because the similarity in DNA sequences of the wheat varieties was over 94%,while that in amino acid sequence was over 96%.And the amino acid sequence difference only can be seen at two sites among some varieties.Phylogenetic tree constructed revealed the evolutionary relationships among these wheat varieties.[Conclusion] This study reveals the polymorphism and evolutionary characteristics in the nucleotide and amino acid sequences in different wheat varieties,which lays foundation for investigating the evolution and biological function of TaUBC4 gene.In addition,the phylogenetic tree constructed provides theoretical references for the classification of the wheat varieties with complicated background.
袁建龙郝英存张祥云赵庆臻
关键词:WHEAT
泛素耦合酶TaUBC是小麦非生物胁迫抗性相关基因
小麦是我国重要的粮食作物,鉴定小麦非生物胁迫响应关键基因,是利用植物基因工程培育对非生物胁迫高耐受性小麦的基础,对我国农业生产具有重要意义。泛素蛋白酶体系统是调节植物生长发育及非生物胁迫应答的重要途径,泛素耦合酶是该系统...
张祥云孙雯雯陈新李鑫虹赵庆臻
关键词:小麦非生物胁迫
小麦TaUBC基因泛素结合酶活性分析被引量:4
2018年
已报道的RNA水平研究表明TaUBC可能是小麦产量相关基因,生物信息学分析显示该基因属于泛素结合酶家族.荧光定量PCR显示TaUBC在小麦根茎叶中均有表达.为了验证TaUBC蛋白是否具有泛素结合酶活性,本文利用原核系统表达野生型TaUBC及三种点突变TaUBC^(C21S)、TaUBC^(C85S)、TaUBC^(C107S)蛋白,并对这些蛋白进行体外泛素化活性分析.结果证实TaUBC是一个有活性的泛素结合酶.另外,点突变C85S使得TaUBC丧失E2活性,C21S和C107S则对活性没有影响,证明其UBC结构域中第85位Cys是结合泛素的关键作用位点.
张祥云赵思语温潇王宁郭彦赵庆臻
关键词:泛素结合酶点突变
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