Profiling of N6-Methyladenosine in Zika Virus RNA and Host Cellular mRNA

Gianluigi Lichinchi1, Tariq M Rana2

  • 1Department of Pediatrics and Institute for Genomic Medicine, University of California San Diego, La Jolla, CA, USA.

Insights

This study introduces a method to map N6-Methylation of adenosine (m6A) in Zika virus RNA and host cell mRNA. Understanding m6A in viral infections is crucial but remains incomplete.

Area of Science:

  • Virology
  • Molecular Biology
  • Epigenetics

Background:

  • N6-Methylation of adenosine (m6A) is a significant posttranscriptional RNA modification found in various viruses, including Zika virus (ZIKV).
  • The precise functions of m6A in viral infections and its impact on the host cell's RNA methylome are not fully understood.
  • Previous studies identified m6A in viruses like Rous sarcoma virus, influenza virus, SV40, HIV-1, and HCV.

Purpose of the Study:

  • To describe an experimental protocol for profiling m6A modifications in ZIKV RNA.
  • To profile m6A modifications in host cell mRNA during ZIKV infection.
  • To advance the understanding of m6A's role in viral RNA and host-virus interactions.

Main Methods:

  • Methylated RNA immunoprecipitation-sequencing (MeRIP-Seq) was employed.
  • The protocol allows for the analysis of m6A "epitranscriptome" in both viral and host RNAs.
  • This technique provides high-resolution mapping of m6A sites.

Main Results:

  • The study presents a detailed protocol for MeRIP-Seq applied to ZIKV RNA and host mRNA.
  • This method enables the generation of m6A profiles for ZIKV RNA.
  • The protocol facilitates the investigation of host cell mRNA methylation changes during viral infection.

Conclusions:

  • The described MeRIP-Seq protocol is a valuable tool for studying m6A modifications in ZIKV RNA.
  • This methodology can elucidate the functional roles of m6A in the context of ZIKV infection.
  • Further research using this protocol can uncover how viral infections alter host RNA methylation dynamics.

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