Abstract
Biological systems function with the aid of large number of proteins involved in complex network of chemical reactions. Interfering with the expression of proteins native or foreign leads to overall changes in the functioning of the biological systems . Manipulating the expression of proteins responsible for the manifestation of diseases has therefore been an interesting area for alternative efficient therapautic possibilities. Proteins are expressed from the correspondig genes involving the trancription and translation of messenger RNAs . Interfering with these RNA has emerged as an effective method of silencing unwanted genes. This project deals with designing effective methods for gene silencing through RNA Interference. RNA interference (RNAi) has emerged as an effective method of silencing gene expression in eukaryotic cells. This technology allows scientists to study the phenotypic effect of reducing expression levels of individual genes, and essentially negates the arduous task of producing single gene knockout or dominant negative expressing cell lines. RNAi has very quickly been utilized both in basic science and medical research. Among its many applications are the characterization and regulation of gene function, signaling pathway analysis and target validation. The potential therapeutic value of RNAi is indicated in recent studies showing that the RNAi pathway is functional in mice and is effective against a variety of infectious diseases including HIV and Hepatitis B. Since the early work describing the use of double-stranded RNA (dsRNA) for post-transcriptional gene silencing (PTGS) by Fire and Mello and the application of short interfering RNA (siRNA) to induce specific gene suppression in mammalian cells by Elbashir et al., there has been a flurry of RNAi-related developments and applications. The vast number of recent scientific journal articles, the scramble for intellectual property, and the formation of multiple biotechnology tools, kits, reagents and therapeutics companies all reflect the power and popularity of this technique. In 2002, Science voted RNAi scientific breakthrough of the year. This paper talks about a novel method of finding efficient siRNA targets on the mRNA sequences. It consists of two parts. In the first part program was written to select suitable targets based on the Elbashir's guidelines. In the second part involves prediction of secondary structure of siRNA antisense strands of the targets predicted in the first part and also the secondary structure of the mRNA sequence, and using these results to further filter the targets.