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N6-methyladenosine modification is not a general trait of viral RNA genomes.


ABSTRACT: Despite the nuclear localization of the m6A machinery, the genomes of multiple exclusively-cytoplasmic RNA viruses, such as chikungunya (CHIKV) and dengue (DENV), are reported to be extensively m6A-modified. However, these findings are mostly based on m6A-Seq, an antibody-dependent technique with a high rate of false positives. Here, we address the presence of m6A in CHIKV and DENV RNAs. For this, we combine m6A-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 m6A modification in CHIKV or DENV transcripts. Furthermore, depletion of key components of the host m6A machinery does not affect CHIKV or DENV infection. Moreover, CHIKV or DENV infection has no effect on the m6A machinery's localization. Our results challenge the prevailing notion that m6A modification is a general feature of cytoplasmic RNA viruses and underscore the importance of validating RNA modifications with orthogonal approaches.

SUBMITTER: Baquero-Perez B 

PROVIDER: S-EPMC10928186 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

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N<sup>6</sup>-methyladenosine modification is not a general trait of viral RNA genomes.

Baquero-Pérez Belinda B   Yonchev Ivaylo D ID   Delgado-Tejedor Anna A   Medina Rebeca R   Puig-Torrents Mireia M   Sudbery Ian I   Begik Oguzhan O   Wilson Stuart A SA   Novoa Eva Maria EM   Díez Juana J  

Nature communications 20240311 1


Despite the nuclear localization of the m<sup>6</sup>A machinery, the genomes of multiple exclusively-cytoplasmic RNA viruses, such as chikungunya (CHIKV) and dengue (DENV), are reported to be extensively m<sup>6</sup>A-modified. However, these findings are mostly based on m<sup>6</sup>A-Seq, an antibody-dependent technique with a high rate of false positives. Here, we address the presence of m<sup>6</sup>A in CHIKV and DENV RNAs. For this, we combine m<sup>6</sup>A-Seq and the antibody-independ  ...[more]

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