水稻(籼稻和粳稻)核小RNA基因全基因组计算分析

M. Shashikanth, A. Snethalatharani, S. Mubarak, K. Ulaganathan
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摘要

对小核RNA (snRNA)基因进行全基因组计算分析,分别从籼稻和粳稻基因组中鉴定出76个和73个推测的snRNA基因。我们使用了与植物snRNA基因至少70%序列一致性的基本标准,用于基因组搜索,存在保守启动子元件:TATA box, USE motif和单子叶启动子特异性元件(MSPs),以及与水稻/植物表达序列标签广泛的序列比对,以表示预测序列为snRNA基因。与其他生物的snRNA基因和预测的二级结构的序列比较分析表明,snRNA序列和结构总体上具有植物特异性特征(在聚合酶II和聚合酶III转录的基因中都存在TATA box,在聚合酶II和聚合酶III转录的snRNA基因中,USE基序在TATA box上游的位置固定但距离不同),并且在USE基序上游存在多个单株特异性MSPs。详细的分析结果包括所有多个序列比对,序列标识,二级结构,序列等可在http://kulab.org上获得
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Genome Wide Computational Analysis of Small Nuclear RNA Genes for Oryza Sativa (Indica and Japonica)
Genome-wide computational analysis for small nuclear RNA (snRNA) genes resulted in identification of 76 and 73 putative snRNA genes from indica and japonica rice genomes, respectively. We used the basic criteria of a minimum of 70 % sequence identity to the plant snRNA gene used for genome search, presence of conserved promoter elements: TATA box, USE motif and monocot promoter specific elements (MSPs) and extensive sequence alignment to rice / plant expressed sequence tags to denote predicted sequence as snRNA genes. Comparative sequence analysis with snRNA genes from other organisms and predicted secondary structures showed that there is overall conservation of snRNA sequence and structure with plant specific features (presence of TATA box in both polymerase II and III transcribed genes, location of USE motif upstream to the TATA box at fixed but different distance in polymerase II and polymerase III transcribed snRNA genes) and the presence of multiple monocot specific MSPs upstream to the USE motif. Detailed analysis results including all multiple sequence alignments, sequence logos, secondary structures, sequences etc are available at http://kulab.org
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