Single-molecule epitranscriptomic analysis of full-length HIV-1 RNAs reveals functional roles of site-specific m6As

Abstract

Although the significance of chemical modifications on RNA is acknowledged, the evolutionary benefits and specific roles in human immunodeficiency virus (HIV-1) replication remain elusive. Most studies have provided only population-averaged values of modifications for fragmented RNAs at low resolution and have relied on indirect analyses of phenotypic effects by perturbing host effectors. Here we analysed chemical modifications on HIV-1 RNAs at the full-length, single RNA level and nucleotide resolution using direct RNA sequencing methods. Our data reveal an unexpectedly simple HIV-1 modification landscape, highlighting three predominant N6-methyladenosine (m6A) modifications near the 3′ end. More densely installed in spliced viral messenger RNAs than in genomic RNAs, these m6As play a crucial role in maintaining normal levels of HIV-1 RNA splicing and translation. HIV-1 generates diverse RNA subspecies with distinct m6A ensembles, and maintaining multiple of these m6As on its RNAs provides additional stability and resilience to HIV-1 replication, suggesting an unexplored viral RNA-level evolutionary strategy.

HIV-1 Infection Reduces NAD Capping of Host Cell snRNA and snoRNA

“…In conclusion, we hypothesize that NAD-capped sRNAs inhibit HIV-1 replication and that part of the virus’s strategy to overcome this inhibition is to reduce the pool of NAD-capped RNA. RNA modifications such as 6-methyladenosine 43 and 2′-O-methylation 44 of the HIV-1 genomic RNA were found to play an important role in HIV-1 infection. Therefore, the NAD cap might be another crucial RNA modification.…”