Modulation of Hepatitis C Virus RNA Abundance by a Liver-Specific MicroRNA

Catherine L. Jopling(The University of Texas Medical Branch at Galveston), MinKyung Yi(The University of Texas Medical Branch at Galveston), Alissa M. Lancaster(The University of Texas Medical Branch at Galveston), Stanley M. Lemon(The University of Texas Medical Branch at Galveston), Peter Sarnow(The University of Texas Medical Branch at Galveston)
Science
September 1, 2005
Cited by 2,495

Abstract

MicroRNAs are small RNA molecules that regulate messenger RNA (mRNA) expression. MicroRNA 122 (miR-122) is specifically expressed and highly abundant in the human liver. We show that the sequestration of miR-122 in liver cells results in marked loss of autonomously replicating hepatitis C viral RNAs. A genetic interaction between miR-122 and the 5' noncoding region of the viral genome was revealed by mutational analyses of the predicted microRNA binding site and ectopic expression of miR-122 molecules containing compensatory mutations. Studies with replication-defective RNAs suggested that miR-122 did not detectably affect mRNA translation or RNA stability. Therefore, miR-122 is likely to facilitate replication of the viral RNA, suggesting that miR-122 may present a target for antiviral intervention.


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