Dataset Information


Hepatitis C virus functionally sequesters miR-122 [HCV vs Mock CLIP]

ABSTRACT: Hepatitis C virus uniquely requires the liver specific microRNA-122 for replication, yet global effects on endogenous miRNA targets during infection are unexplored. Here, high-throughput sequencing and crosslinking immunoprecipitation (HITS-CLIP) experiments of human Argonaute (Ago) during HCV infection showed robust Ago binding on the HCV 5’UTR, at known and predicted miR-122 sites. On the human transcriptome, we observed reduced Ago binding and functional mRNA de-repression of miR-122 targets during virus infection. This miR-122 “sponge” effect could be relieved and redirected to miR-15 targets by swapping the miRNA tropism of the virus. Single-cell expression data from reporters containing miR-122 sites showed significant de-repression during HCV infection depending on expression level and number of sites. We describe a quantitative mathematical model of HCV induced miR-122 sequestration and propose that such miR-122 inhibition by HCV RNA may result in global de-repression of host miR-122 targets, providing an environment fertile for the long-term oncogenic potential of HCV. AGO HITS-CLIP libraries were generated from mock or J6/JFH1 Clone2 infected Huh7.5 cells. Cells were infected at an MOI of 1-2 and harvested 72hours post-infection for CLIP. Libraries were generated with a 4nt index read, a common priming sequence, followed by a 5nt degenerate barcode terminiating in a G. Files have been demultiplexed such that the 5nt degenerate barcode has been appended as the first 5 nucleotides of the read.

ORGANISM(S): Homo sapiens  

SUBMITTER: Ira M Jacobson   Robert B Darnell  Aldo Mele  Eiko Nishiuchi  John J Fak  Charles M Rice  Maria T Catanese  Constantin N Takacs  Katharina S Shaw  Joseph M Luna  Troels K Scheel  Tal Danino  Ype P de Jong 

PROVIDER: E-GEOD-64675 | ArrayExpress | 2015-01-06



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