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Updated: Feb 1, 2026

A Method for Measuring RNA N6-methyladenosine Modifications in Cells and Tissues
Published on: December 5, 2016
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.
Abstract:
N6-Methylation of adenosine (m6A) in viral RNA was first identified in Rous sarcoma virus, influenza virus, and SV40 virus several decades ago. More recently, human immunodeficiency virus-1, hepatitis C virus, and Zika virus (ZIKV) RNAs have also been reported to be modified by m6A, highlighting the significance of this posttranscriptional RNA modification. Nevertheless, the functions of m6A and their roles in the context of viral infections are not completely understood. Similarly, the mechanisms by which viral infections may alter the dynamics of the host RNA methylome have yet to be elucidated. Here, we describe an experimental protocol to obtain m6A profiles of ZIKV RNA and the host cell mRNA using methylated RNA immunoprecipitation-sequencing (MeRIP-Seq).
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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