内含子选择性聚腺苷化位点的预测方法。

Shanxin Zhang
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引用次数: 0

摘要

mrna的选择性聚腺苷化(APA)已被证明是转录后基因调控的重要机制。内含子APA和剪接之间的相互作用可能影响mrna的同工型。在本文中,我们发现了四个普遍的基序,即AATAAA, TTTTTTTT, CCAGSCTGG和RGYRYRGTGG围绕聚腺苷化位点;在此基础上,提出了一种基于加权度字符串核的支持向量机(SVM)的人类基因组内含子APA位点识别方法。与其他APA事件相比,内含子APA位点可能为TTTTTTTT模式。所提出的算法可以正确地将89%的内含子APA位点从组成型聚腺苷化位点中分类出来。此外,内含子型APA与其他类型APA的预测准确率可达88.3%。预测结果表明,我们的计算方法在内含子APA位点的识别上是有希望的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prediction method for Intronic alternative polyadenylation sites.
Alternative Polyadenylation (APA) of mRNAs has been proven as a considerable mechanism for post-transcriptional gene regulation. The interplay between Intronic APA and splicing may affect the isoforms of mRNAs. In this paper, we have found four prevalent motifs, i.e. AATAAA, TTTTTTTT, CCAGSCTGG and RGYRYRGTGG surrounding the polyadenylation sites; then we proposed a new computational method to identify the Intronic APA sites in the human genome, which is based on a Support Vector Machine (SVM) with weighted degree string kernel. Compared with other APA events, Intronic APA sites are likely to be with TTTTTTTT pattern. The proposed algorithm can correctly classify 89% of Intronic APA sites from the constitutive polyadenylation sites. In addition, the prediction accuracy of separating the Intronic APA from other types of APA could be up to 88.3%. The prediction results indicate that our computational method is promising for the identification of Intronic APA sites.
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CiteScore
2.20
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