Evidence for natural antisense transcript-mediated inhibition of microRNA function.docVIP

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Evidence for natural antisense transcript-mediated inhibition of microRNA function.doc

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Evidence for natural antisense transcript-mediated inhibition of microRNA function

Faghihi et al. Genome Biology 2010, 11:R56 /2010/11/5/R56 RESEARCH Open Access Evidence for natural antisense transcript-mediated Research inhibition of microRNA function Mohammad Ali Faghihi1, Ming Zhang3,4, Jia Huang5, Farzaneh Modarresi1, Marcel P Van der Brug1, Michael A Nalls6, Mark R Cookson6, Georges St-Laurent III7 and Claes Wahlestedt*1,2 Abstract Background: MicroRNAs (miRNAs) have the potential to regulate diverse sets of mRNA targets. In addition, mammalian genomes contain numerous natural antisense transcripts, most of which appear to be non-protein-coding RNAs (ncRNAs). We have recently identified and characterized a highly conserved non-coding antisense transcript for beta-secretase-1 (BACE1), a critical enzyme in Alzheimers disease pathophysiology. The BACE1-antisense transcript is markedly up-regulated in brain samples from Alzheimers disease patients and promotes the stability of the (sense) BACE1 transcript. Results: We report here that BACE1-antisense prevents miRNA-induced repression of BACE1 mRNA by masking the binding site for miR-485-5p. Indeed, miR-485-5p and BACE1-antisense compete for binding within the same region in the open reading frame of the BACE1 mRNA. We observed opposing effects of BACE1-antisense and miR-485-5p on BACE1 protein in vitro and showed that Locked Nucleic Acid-antimiR mediated knockdown of miR-485-5p as well as BACE1-antisense over-expression can prevent the miRNA-induced BACE1 suppression. We found that the expression of BACE1-antisense as well as miR-485-5p are dysregulated in RNA samples from Alzheimers disease subjects compared to control individuals. Conclusions: Our data demonstrate an interface between two distinct groups of regulatory RNAs in the computation of BACE1 gene expression. Moreover, bioinformatics analyses revealed a theoretical basis for many other potential interactions between natural antisense transcripts and miRNAs at the binding sites of the latter. Background found well cons