Epitranscriptomic cytidine methylation of the hepatitis B viral RNA is essential for viral reverse transcription and particle production
Pei-Yi Su, C Y Chang, Shin-Chwen Bruce Yen, Hsiu-Yi Wu, Wan-Ju Tung, Yu-Pei Hu, Yen-Yu Ian Chen, Miao‐Hsia Lin, Chiaho Shih, Pei‐Jer Chen, Kevin Tsai
Abstract
Epitranscriptomic RNA modifications have emerged as important regulators of the fate and function of viral RNAs. One prominent modification, the cytidine methylation 5-methylcytidine (m 5 C), is found on the RNA of HIV-1, where m 5 C enhances the translation of HIV-1 RNA. However, whether m 5 C functionally enhances the RNA of other pathogenic viruses remains elusive. Here, we surveyed a panel of commonly found RNA modifications on the RNA of hepatitis B virus (HBV) and found that HBV RNA is enriched with m 5 C as well as ten other modifications, at stoichiometries much higher than host messenger RNA (mRNA). Intriguingly, m 5 C is mostly found on the epsilon hairpin, an RNA element required for viral RNA encapsidation and reverse transcription, with these m 5 C mainly deposited by the cellular methyltransferase NSUN2. Loss of m 5 C from HBV RNA due to NSUN2 depletion resulted in a partial decrease in viral core protein (HBc) production, accompanied by a near-complete loss of the reverse transcribed viral DNA. Similarly, mutations introduced to remove the methylated cytidines resulted in a loss of HBc production and reverse transcription. Furthermore, pharmacological disruption of m 5 C deposition led to a significant decrease in HBV replication. Thus, our data indicate m 5 C methylations as a critical mediator of the epsilon elements’ function in HBV virion production and reverse transcription, suggesting the therapeutic potential of targeting the m 5 C methyltransfer process on HBV epsilon as an antiviral strategy.