In-Silico Algorithms for the Screening of Possible microRNA Binding Sites and Their Interactions.

In-Silico Algorithms for the Screening of Possible microRNA Binding Sites and Their Interactions. Curr Genomics. 2013 Apr;14(2):127-36 Authors: Dweep H, Sticht C, Gretz N Abstract MicroRNAs (miRNAs) comprise a recently discovered class of small, non-coding RNA molecules of 21-25 nucleotides in length that regulate the gene expression by base-pairing with the transcripts of their targets i.e. protein-coding genes, leading to down-regulation or repression of the target genes. However, target gene activation has also been described. miRNAs are involved in diverse regulatory pathways, including control of developmental timing, apoptosis, cell proliferation, cell differentiation, modulation of immune response to macrophages, and organ development and are associated with many diseases, such as cancer. Computational prediction of miRNA targets is much more challenging in animals than in plants, because animal miRNAs often perform imperfect base-pairing with their target sites, unlike plant miRNAs which almost always bind their targets with near perfect complementarity. In the past years, a large number of target prediction programs and databases on experimentally validated information have been developed for animal miRNAs to fulfil the need of experimental scientists conducting miRNA research. In this review we first succinctly describe the prediction criteria (rules or principles) adapted by prediction algorithms to generate possible miRNA...
Source: Current Genomics - Category: Genetics & Stem Cells Tags: Curr Genomics Source Type: research