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Altered proteolytic processing of the polymerase polyprotein in RNA(-) temperature sensitive mutants of murine
1Department of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL 60153.
Abstract:
We examined the synthesis and processing of the polymerase polyprotein in RNA(-) temperature sensitive mutant of murine coronavirus strain A59. These temperature sensitive mutants of MHV-A59 synthesize viral RNA at the permissive temperature (33.0 degrees C), but are unable to synthesize viral RNA at the nonpermissive temperature (39.5 degrees C). The ts mutants have been mapped to five different complementation groups in the polymerase gene. The 5'-most complementation groups, Groups A and B, map to a region encoding an autoproteinase responsible for the cleavage of p28, the amino-terminal product of the polymerase polyprotein. We screened six temperature sensitive mutants to determine if there was an alteration in the proteolytic processing of the polymerase polyprotein, particularly in the cleavage of the p28 protein. Two mutants, tsNC9 and tsLA16, had altered proteolytic products at both the permissive and nonpermissive temperatures. One Group B temperature sensitive mutant, designated tsNC11, was defective in the production of p28 protein at the nonpermissive temperature. To further localize the site of the mutation in tsNC11, RNA representing the 5'-most 5.3 kb region of the polymerase gene was transfected into tsNC11-infected cells and virus production monitored. The transfected RNA was able to complement the defect in tsNC11, resulting in viral RNA synthesis and production of viral particles at the nonpermissive temperature. These results indicate that a gene product from the 5.3 kb region of gene 1 is required for coronavirus RNA synthesis.
Insights
Murine coronavirus temperature-sensitive mutants reveal a critical gene product within the 5.3 kb region of gene 1, essential for viral RNA synthesis and replication.
Area of Science:
- Virology
- Molecular Biology
- Genetics
Background:
- Murine coronavirus (MHV-A59) temperature-sensitive (ts) mutants exhibit defects in viral RNA synthesis at non-permissive temperatures.
- These ts mutants have been mapped to five complementation groups within the polymerase gene.
Purpose of the Study:
- To investigate the synthesis and processing of the polymerase polyprotein in MHV-A59 ts mutants.
- To identify specific mutations affecting viral RNA synthesis and polymerase polyprotein processing.
Main Methods:
- Screening of six ts mutants for alterations in polymerase polyprotein processing, focusing on p28 cleavage.
- Complementation analysis by transfecting RNA from the 5'-most 5.3 kb region of the polymerase gene into ts mutant-infected cells.
Main Results:
- Two mutants (tsNC9, tsLA16) showed altered proteolytic products at both permissive and non-permissive temperatures.
- A Group B mutant (tsNC11) was defective in p28 production at the non-permissive temperature.
- Transfection of the 5.3 kb RNA region restored viral RNA synthesis and particle production in tsNC11-infected cells.
Conclusions:
- A gene product encoded within the 5.3 kb region of MHV gene 1 is essential for coronavirus RNA synthesis.
- This finding localizes a critical component for viral replication to a specific region of the polymerase gene.