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Updated: Oct 4, 2026

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus
Published on: July 27, 2021
Cooperation of an RNA packaging signal and a viral envelope protein in coronavirus RNA packaging
1Department of Microbiology and Immunology, The University of Texas Medical Branch at Galveston, Galveston, Texas 77555-1019, USA.
Abstract:
Murine coronavirus mouse hepatitis virus (MHV) produces a genome-length mRNA, mRNA 1, and six or seven species of subgenomic mRNAs in infected cells. Among these mRNAs, only mRNA 1 is efficiently packaged into MHV particles. MHV N protein binds to all MHV mRNAs, whereas envelope M protein interacts only with mRNA 1. This M protein-mRNA 1 interaction most probably determines the selective packaging of mRNA 1 into MHV particles. A short cis-acting MHV RNA packaging signal is necessary and sufficient for packaging RNA into MHV particles. The present study tested the possibility that the selective M protein-mRNA 1 interaction is due to the packaging signal in mRNA 1. Regardless of the presence or absence of the packaging signal, N protein bound to MHV defective interfering RNAs and intracellularly expressed non-MHV RNA transcripts to form ribonucleoprotein complexes; M protein, however, interacted selectively with RNAs containing the packaging signal. Moreover, only the RNA that interacted selectively with M protein was efficiently packaged into MHV particles. Thus, it was the packaging signal that mediated the selective interaction between M protein and viral RNA to drive the specific packaging of RNA into virus particles. This is the first example for any RNA virus in which a viral envelope protein and a known viral RNA packaging signal have been shown to determine the specificity and selectivity of RNA packaging into virions.
Insights
Mouse hepatitis virus (MHV) selectively packages mRNA 1 using its M protein and a specific RNA packaging signal. This signal mediates M protein interaction, ensuring efficient viral RNA packaging into new virions.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- Murine coronavirus (MHV) produces multiple mRNAs, but only mRNA 1 is packaged into virions.
- MHV N protein binds all viral mRNAs, while M protein selectively binds mRNA 1.
- A cis-acting RNA packaging signal is crucial for MHV RNA packaging.
Purpose of the Study:
- To investigate if the packaging signal in mRNA 1 mediates the selective interaction with M protein.
- To determine the role of the packaging signal in specific RNA packaging into MHV particles.
Main Methods:
- Testing M protein interaction with RNAs containing or lacking the packaging signal.
- Analyzing the packaging efficiency of RNAs that interact with M protein.
- Utilizing MHV defective interfering RNAs and non-MHV RNA transcripts.
Main Results:
- M protein selectively interacted with RNAs possessing the MHV packaging signal, irrespective of N protein binding.
- Only RNAs that selectively interacted with M protein were efficiently packaged into MHV particles.
- The packaging signal was identified as the mediator of selective M protein-RNA interaction.
Conclusions:
- The MHV packaging signal dictates the selective M protein-RNA interaction, driving specific RNA packaging.
- This study provides the first evidence for an RNA virus where an envelope protein and packaging signal jointly ensure selective RNA packaging into virions.
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