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SpliceAid 2: a database of human splicing factors expression data and RNA target motifs.

机译:SpliceAid 2:人剪接因子表达数据和RNA靶基序的数据库。

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摘要

Splicing is the most frequently altered biological process by mutations within gene regions. Information for splicing is recognized by several factors that bind pre-mRNA sequence and, through coordinated interaction, yield mature transcripts. Some in silico methods have been developed to predict if a mutation leads to aberrant splicing patterns. We previously created SpliceAid tool that is able to minimize false positive predictions because it adopts strictly experimental RNA target motifs bound by splicing proteins in humans. In order to improve prediction accuracy and better understand the splicing outcome, the tissue specificity of each splicing regulatory factor has to be taken into account. Here, we have developed SpliceAid 2 by adding the expression data related to the splicing factors extracted from the main proteomic and transcriptomic databases, true 5' and 3' splice sites, polypyrimidine tracts, and branch point sequences. The new version collects 2,220 target sites of 62 human splicing proteins and their expression data in 320 tissues per cell. SpliceAid 2 can be useful to foresee the splicing pattern alteration, to guide the identification of the molecular effect due to the mutations and to understand the tissue-specific alternative splicing. SpliceAid 2 is freely accessible at www.introni.it/spliceaid.html.
机译:剪接是通过基因区域内的突变最常改变的生物学过程。剪接信息可通过结合前mRNA序列的几种因素来识别,并通过协调相互作用产生成熟的转录本。已经开发了一些计算机方法,以预测突变是否导致异常的剪接模式。我们以前创建了SpliceAid工具,该工具能够将假阳性预测降到最低,因为它采用了严格的实验性RNA靶基序,这些基序是由人类的剪接蛋白所束缚的。为了提高预测准确性并更好地理解剪接结果,必须考虑每个剪接调节因子的组织特异性。在这里,我们通过添加与从主要的蛋白质组学和转录组学数据库,真正的5'和3'剪接位点,多嘧啶片段和分支点序列中提取的剪接因子相关的表达数据,开发了SpliceAid 2。新版本收集了62个人类剪接蛋白的2,220个靶位点,并在每个细胞的320个组织中表达了它们的表达数据。 SpliceAid 2可用于预见剪接模式的改变,指导对由于突变引起的分子效应的识别以及了解组织特异性的替代剪接。可在www.introni.it/spliceaid.html上免费访问SpliceAid 2。

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