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Cloning and Identification of Differentially Expressed Genes Associated with Smut in Sugarcane

机译:甘蔗中黑穗病相关差异表达基因的克隆与鉴定

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The aim of this experiment was to evaluate the molecular mechanism of sugarcane response to the smut pathogen at the beginning of the pathogen infection of sugarcane seedlings, to explore related genes, and to provide useful information for developing rational strategies to control smut at early stages of disease development. A suppression subtractive hybridization library was constructed using cDNA synthesized from RNA extracted from normal stalks as driver and inoculated stalks as tester. The positive clones of the libraries were sequenced randomly, analyzed by BLAST, and classified by GO. A total of 248 positive clones were selected for sequencing, and a total of 224 EST sequences were obtained. In total, 188 ESTs were found to share a considerable homology with known genes, while the remaining 36 ESTs had no homology with known genes. In the Gene Ontology database, the unigenes were assigned functional descriptions; 152, 129, and 139 ESTs were, respectively, involved in cell component, molecular function, and biological process. Some genes related to a smut pathogen infection were obtained, while the SSH library was constructed. These genes reflected the regulation of sugarcane to smut pathogen and can be used as candidate genes.
机译:本实验的目的是评估在甘蔗幼苗病原体感染开始时甘蔗对黑曲病病原菌反应的分子机制,探索相关基因,并为制​​定合理的策略控制甘蔗早期的黑曲病提供有用的信息。疾病发展。利用从正常茎提取的RNA中合成的cDNA作为驱动因子,并以接种后的茎作为测试者,构建了抑制消减杂交文库。对文库的阳性克隆进行随机测序,BLAST分析和GO分类。总共选择了248个阳性克隆进行测序,并获得了224个EST序列。总共发现188个EST与已知基因具有相当的同源性,而其余36个EST与已知基因没有同源性。在基因本体数据库中,为单基因分配了功能描述;分别有152、129和139个EST与细胞成分,分子功能和生物学过程有关。获得了一些与黑穗病菌感染有关的基因,同时构建了SSH文库。这些基因反映了甘蔗对致病菌的调节,可以用作候选基因。

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