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利用统计和聚类技术选择有效小干扰RNA序列的方法。

Methods for selecting effective siRNA sequences by using statistical and clustering techniques.

作者信息

Takasaki Shigeru

机构信息

RIKEN Genomic Sciences Center, Yokohama, Kanagawa, Japan.

出版信息

Methods Mol Biol. 2009;487:1-39. doi: 10.1007/978-1-60327-547-7_1.

DOI:10.1007/978-1-60327-547-7_1
PMID:19301640
Abstract

Short interfering RNAs (siRNAs) have been widely used for studying gene functions in mammalian cells but vary markedly in their gene-silencing efficacy. Although many design rules/guidelines for effective siRNAs based on various criteria have been reported recently, there are only a few consistencies among them. This makes it difficult to select effective siRNA sequences targeting mammalian genes. This chapter first reviews the reported siRNA design guidelines and clarifies the problems concerning the current guidelines. It then describes the recently reported new scoring methods for selecting effective siRNA sequences by using statistics and clustering techniques such as the self-organizing map (SOM) and the radial basis function (RBF) network. In the proposed three methods, individual scores are defined as a gene degradation measure based on position-specific statistical significances. The effectiveness of the methods was confirmed by evaluating effective and ineffective siRNAs for recently reported genes and comparison with other reported scoring methods. The sizes (values) of these scores are closely correlated with the degree of gene degradation, and the scores can easily be used for selecting high-potential siRNA candidates. The evaluation results indicate that the proposed new methods are useful for selecting siRNA sequences targeting mammalian mRNA sequences.

摘要

短干扰RNA(siRNA)已被广泛用于研究哺乳动物细胞中的基因功能,但其基因沉默效率差异显著。尽管最近有许多基于各种标准的有效siRNA设计规则/指南被报道,但它们之间只有少数一致性。这使得选择靶向哺乳动物基因的有效siRNA序列变得困难。本章首先回顾已报道的siRNA设计指南,并阐明当前指南存在的问题。然后描述最近报道的通过使用自组织映射(SOM)和径向基函数(RBF)网络等统计和聚类技术来选择有效siRNA序列的新评分方法。在所提出的三种方法中,个体评分被定义为基于位置特异性统计显著性的基因降解度量。通过评估最近报道基因的有效和无效siRNA并与其他报道的评分方法进行比较,证实了这些方法的有效性。这些评分的值与基因降解程度密切相关,并且这些评分可轻松用于选择高潜力的siRNA候选物。评估结果表明,所提出的新方法对于选择靶向哺乳动物mRNA序列的siRNA序列很有用。

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引用本文的文献

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Preclinical and clinical development of siRNA-based therapeutics.基于小干扰RNA的治疗药物的临床前和临床开发。
Adv Drug Deliv Rev. 2015 Jun 29;87:108-19. doi: 10.1016/j.addr.2015.01.007. Epub 2015 Feb 7.