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首页> 外文期刊>Biological & pharmaceutical bulletin >Transcriptional Activation of Putative Calmodulin Genes Am-cam-1 and Am-cam-2 from Aquilaria microcarpa, in Response to External Stimuli
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Transcriptional Activation of Putative Calmodulin Genes Am-cam-1 and Am-cam-2 from Aquilaria microcarpa, in Response to External Stimuli

机译:小果沉香的假定钙调蛋白基因Am-cam-1和Am-cam-2的转录激活响应外部刺激。

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摘要

A homology-based cloning strategy yielded two cDNA clones designated Am-cam-1 and Am-cam-2, presumably encoding calmodulin protein from a callus culture derived from the leaf tissues of Aquilaria microcarpa. An appreciable increase in the transcriptional activity of Am-cam-1 was reproducibly observed by exposure of the cell culture to methyl jasmonate, as analyzed by a reverse-transcription polymerase chain reaction. The expression level of the gene also increased when the cells were treated with yeast extract. The transcription of Am-cam-2 was similarly stimulated by the treatment with methyl jasmonate and yeast extract, however, the intensities of the enhanced expression appeared to be lower as compared with that of Am-cam-1. In contrast, Ca2+-ionophore A23187 did not show inducing activity for the expression of these two calmodulin genes. These results suggest that Am-cam-1 and Am-cam-2 and their products play important roles in signal transduction processes in methyl jasmonate- and yeast extract-treated cells of A. microcarpa, accompanying the change in the transcriptional activities.
机译:基于同源性的克隆策略产生了两个名为Am-cam-1和Am-cam-2的cDNA克隆,大概是编码来自小木沉香叶组织的愈伤组织培养物中的钙调蛋白。如通过逆转录聚合酶链反应所分析的,通过将细胞培养物暴露于茉莉酸甲酯,可再现地观察到Am-cam-1的转录活性明显增加。当用酵母提取物处理细胞时,基因的表达水平也增加。茉莉酸甲酯和酵母提取物处理类似地刺激了Am-cam-2的转录,但是,与Am-cam-1相比,增强表达的强度似乎更低。相反,Ca 2+-离子载体A23187没有显示出对这两个钙调蛋白基因表达的诱导活性。这些结果表明,Am-cam-1和Am-cam-2及其产品在茉莉酸甲酯和酵母提取物处理过的小果曲霉细胞中的信号转导过程中起着重要作用,伴随着转录活性的变化。

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