<i>N6</i> -methyladenosine modification of hepatitis B virus RNA differentially regulates the viral life cycle

Hasan Imam(University of California San Diego), Mohsin Khan(University of California San Diego), Nandan S. Gokhale(Duke Medical Center), Alexa B. R. McIntyre(Cornell University), Geon‐Woo Kim(Yonsei University), Jae Young Jang(Soonchunhyang University), Seong‐Jun Kim(Korea Research Institute of Chemical Technology), Christopher E. Mason(Cornell University), Stacy M. Horner(Duke Medical Center), Aleem Siddiqui(University of California San Diego)
Proceedings of the National Academy of Sciences
August 13, 2018
Cited by 234Open Access
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Abstract

Significance N6 -methyladenosine (m 6 A) has recently been found to regulate numerous aspects of RNA biology. Similar to methylation of cytosine residues in DNA, eukaryotic RNA is modified by enzymatic addition of methyl groups at adenosines. m 6 A modification of RNA affects a wide variety of RNA functions, including mRNA stability, translation, and in the case of viruses, viral replication and production. Our investigation revealed that the adenosine residues present in the known m 6 A consensus motif within the 5′ epsilon stem loop of pregenomic RNA and the 3′ ends of all the hepatitis B virus (HBV) transcripts are m 6 A modified. We demonstrate here that m 6 A modification differentially modulates HBV RNA stability and reverse transcription, thereby playing two distinct regulatory roles in the HBV life cycle.


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