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首页> 外文期刊>Electronic Journal of Biotechnology >Analysis of gene expression in Kalanchoe daigremontiana leaves during plantlet formation under drought stress
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Analysis of gene expression in Kalanchoe daigremontiana leaves during plantlet formation under drought stress

机译:干旱胁迫下Kalanchoe daigremontiana叶片幼苗形成过程中的基因表达分析

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Background: Kalanchoe daigremontiana is an attractive model system for the study of the molecular mechanisms of somatic embryogenesis and organogenesis competence due to its formation of plantlets with adventitious roots on the leaf margins that are derived from somatic embryos. The suppression subtractive hybridization technique was used to investigate gene expression during asexual reproduction. Leaves from plants subjected to drought stress provided the source of ‘Tester’ DNA, and leaves from plants grown under normal conditions provided the ‘Driver’ DNA for subtractive hybridization.Results: A total of 481 high quality ESTs were generated, which clustered into 390 unigenes. Of these unigenes, 132 grouped into 12 functional categories, suggesting that asexual reproduction is a complicated process involving a large number of genes. The expression characteristics of selected genes from the SSH library were determined by real-time PCR and were classified into five groups, suggesting that gene expression patterns during asexual reproduction are complex. Up-regulation of S-adenosylhomocysteine hydrolase suggested that a decrease in cytokinin levels promotes the initiation of plantlet formation. Many other genes, such as inorganic pyrophosphatase and glutamate decarboxylase, play important roles in gene regulation during asexual reproduction.Conclusion: Our results provide a framework and unified platform on which future research on asexual reproduction in K. daigremontiana can be based. This represents the first genome-wide study of asexual reproduction in K. daigremontiana.
机译:背景:Kalanchoe daigremontiana是一个吸引人的模型系统,用于研究体细胞胚发生和器官发生能力的分子机制,这是由于其形成的小植株具有不定根,其起源于体细胞胚。抑制消减杂交技术用于研究无性繁殖过程中的基因表达。遭受干旱胁迫的植物叶片提供了'Tester'DNA的来源,而在正常条件下生长的植物叶片则提供了'Driver'DNA进行减性杂交。结果:总共产生了481个高质量的EST,聚集成了390个单基因。在这些单基因中,有132个分为12个功能类别,这表明无性繁殖是一个涉及大量基因的复杂过程。通过实时PCR确定了来自SSH文库的选定基因的表达特征,并将其分为五个组,这表明无性繁殖过程中的基因表达模式是复杂的。 S-腺苷同型半胱氨酸水解酶的上调表明细胞分裂素水平的降低促进了幼苗形成的开始。其他许多基因,例如无机焦磷酸酶和谷氨酸脱羧酶,在无性繁殖过程中也起着重要的基因调控作用。结论:我们的结果提供了一个框架和统一的平台,可以作为今后对无花果无性繁殖的研究的基础。这代表了对K. daigremontiana中无性繁殖的第一个全基因组研究。

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