Park Young-Kyu, Park Seong-Min, Choi Young-Chul, Lee Doheon, Won Misun, Kim Young Joo
Medical Genomics Research Center, KRIBB, Daejeon 305-806, Korea.
Nucleic Acids Res. 2008 Jul 1;36(Web Server issue):W97-103. doi: 10.1093/nar/gkn280. Epub 2008 May 14.
RNA interference (RNAi) with small interfering RNA (siRNA) has become a powerful tool in functional and medical genomic research through directed post-transcriptional gene silencing. In order to apply RNAi technique for eukaryotic organisms, where frequent alternative splicing results in diversification of mRNAs and finally of proteins, we need spliced mRNA isoform silencing to study the function of individual proteins. AsiDesigner is a web-based siRNA design software system, which provides siRNA design capability to account for alternative splicing for mRNA level gene silencing. It provides numerous novel functions including the designing of common siRNAs for the silencing of more than two mRNAs simultaneously, a scoring scheme to evaluate the performance of designed siRNAs by adopting currently known key design factors, a stepwise off-target searching with BLAST and FASTA algorithms and checking the folding secondary structure energy of siRNAs. To do this, we developed a novel algorithm to evaluate the common target region, where siRNAs can be designed to knockdown a specific mRNA isoform or more than two mRNA isoforms from a target gene simultaneously. The developed algorithm and the AsiDesigner were tested and validated as very effective throughout widely performed gene silencing experiments. It is expected that AsiDesigner will play an important role in functional genomics, drug discovery and other molecular biological research. AsiDesigner is freely accessible at http://sysbio.kribb.re.kr/AsiDesigner/.
通过小干扰RNA(siRNA)进行的RNA干扰(RNAi),已成为功能基因组学和医学基因组学研究中一种强大的工具,它可实现定向的转录后基因沉默。为了将RNAi技术应用于真核生物,由于真核生物中频繁的可变剪接会导致mRNA以及最终蛋白质的多样化,因此我们需要实现剪接的mRNA异构体沉默,以便研究单个蛋白质的功能。AsiDesigner是一个基于网络的siRNA设计软件系统,它提供了考虑可变剪接的siRNA设计功能,可在mRNA水平上实现基因沉默。它具有许多新颖的功能,包括设计可同时沉默两个以上mRNA的通用siRNA、通过采用当前已知的关键设计因素来评估设计的siRNA性能的评分方案、使用BLAST和FASTA算法进行逐步脱靶搜索以及检查siRNA的折叠二级结构能量。为此,我们开发了一种新颖的算法来评估共同靶区域,在该区域可以设计siRNA以同时敲低特定的mRNA异构体或来自靶基因的两个以上mRNA异构体。在广泛进行的基因沉默实验中,所开发的算法和AsiDesigner经过测试和验证,被证明非常有效。预计AsiDesigner将在功能基因组学、药物发现和其他分子生物学研究中发挥重要作用。可通过http://sysbio.kribb.re.kr/AsiDesigner/免费访问AsiDesigner。