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N 6 -methyladenosine modification is not a general trait of viral RNA genomes.

Belinda Baquero-PerezIvaylo D YonchevAnna Delgado-TejedorRebeca MedinaMireia Puig-TorrentsIan M SudberyOguzhan BegikStuart A WilsonEva Maria NovoaJuana Díez
Published in: Nature communications (2024)
Despite the nuclear localization of the m 6 A machinery, the genomes of multiple exclusively-cytoplasmic RNA viruses, such as chikungunya (CHIKV) and dengue (DENV), are reported to be extensively m 6 A-modified. However, these findings are mostly based on m 6 A-Seq, an antibody-dependent technique with a high rate of false positives. Here, we address the presence of m 6 A in CHIKV and DENV RNAs. For this, we combine m 6 A-Seq and the antibody-independent SELECT and nanopore direct RNA sequencing techniques with functional, molecular, and mutagenesis studies. Following this comprehensive analysis, we find no evidence of m 6 A modification in CHIKV or DENV transcripts. Furthermore, depletion of key components of the host m 6 A machinery does not affect CHIKV or DENV infection. Moreover, CHIKV or DENV infection has no effect on the m 6 A machinery's localization. Our results challenge the prevailing notion that m 6 A modification is a general feature of cytoplasmic RNA viruses and underscore the importance of validating RNA modifications with orthogonal approaches.
Keyphrases
  • dengue virus
  • zika virus
  • aedes aegypti
  • single cell
  • genome wide
  • rna seq
  • nucleic acid
  • sars cov
  • multidrug resistant
  • deep learning
  • genome wide association