首页> 外文期刊>Australian Journal of Crop Science >Cloning and identification of a differentially expressed RING E3 ubiquitin-protein ligase gene responding to Jasmonic acid signaling pathway in rubber tree (Hevea brasiliensis)
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Cloning and identification of a differentially expressed RING E3 ubiquitin-protein ligase gene responding to Jasmonic acid signaling pathway in rubber tree (Hevea brasiliensis)

机译:橡胶树茉莉酸信号通路的差异表达RING E3泛素蛋白连接酶基因的克隆与鉴定

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In order to understand the key metabolic pathways and key genes involved in the latex biosynthesis process in rubber tree, we studied the differential gene expression between latex and leaves of rubber tree by cDNA microarray. The significant analysis of microarray (SAM) method was used, and genes that were differentially expressed in the latex and leaves of rubber tree were selected and subjected to various analyses of KEGG metabolic pathway, clustering, and gene ontology based biological pathways. The results indicated that many differentially expression genes mainly distribute in transcription factor activity, zinc ion binding, transferase activity, ubiquitin-protein ligase activity. One of the zinc finger protein encoded genes, named HbRBX1, which involves in transcription factor activity, zinc ion binding, ubiquitin-protein ligase activity, was cloned and further confirmed the expression patterns in rubber tree latex and rubber tree leaves by Semi-quantitative RT PCR. In order to understand whether the HbRBX1 involve in latex biosynthesis or not, the HbRBX1 expression patterns were also analyzed in response to exogenous jasmonic acid and ethylene, the two types of phytohormone have been proved to involve in latex biosynthesis in rubber tree, the results showed that HbRBX1 can respond to exogenous jasmonic acid while cannot respond to exogenous ethylene, suggested that HbRBX1 maybe participate in the latex biosynthesis through the jasmonic acid pathway.
机译:为了了解橡胶树胶乳生物合成过程中的关键代谢途径和关键基因,我们通过cDNA微阵列技术研究了橡胶树胶乳与叶片之间的差异基因表达。使用显着分析微阵列(SAM)方法,并选择在橡胶树的乳胶和叶子中差异表达的基因,并对KEGG代谢途径,聚类和基于基因本体的生物途径进行各种分析。结果表明,许多差异表达基因主要分布在转录因子活性,锌离子结合,转移酶活性,泛素蛋白连接酶活性上。克隆了一种锌指蛋白编码基因HbRBX1,其涉及转录因子活性,锌离子结合,泛素蛋白连接酶活性,并通过半定量RT进一步证实了在橡胶树胶乳和橡胶树中的表达模式。 PCR。为了了解HbRBX1是否参与了乳胶的生物合成,还针对外源茉莉酸和乙烯对HbRBX1的表达模式进行了分析,证明了两种植物激素均参与了橡胶树的乳胶生物合成,结果表明HbRBX1可以响应外源茉莉酸而不能响应外源乙烯,提示HbRBX1可能通过茉莉酸途径参与了乳胶的生物合成。

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