Differential activation of the influenza virus polymerase via template RNA binding
- PMID: 7769657
- PMCID: PMC189131
- DOI: 10.1128/JVI.69.7.3995-3999.1995
Differential activation of the influenza virus polymerase via template RNA binding
Abstract
Primary transcripts synthesized by the influenza virus polymerase contain the capped 5' ends of eukaryotic mRNAs. These sequences are derived from host mRNA and scavenged by the viral polymerase as a prerequisite to transcription. The first step in this reaction is the specific binding of the viral polymerase to the cap structure of the host RNA. The role that template RNA plays in this RNA binding reaction was examined in quantitative capped mRNA binding and endonuclease assays. Capped RNA binding was shown to be a template-dependent property of the influenza virus polymerase. Addition of only the 5' end of viral RNA stimulates capped mRNA binding by the viral polymerase, but endonuclease activity requires the addition of the 3' end. The addition of template RNA corresponding to the positive-sense complementary RNA replicative intermediate was also able to stimulate capped mRNA binding but was not able to efficiently activate the viral endonuclease. Thus, regulation of endonuclease activity by the influenza virus polymerase can be dependent on template RNA binding.
Similar articles
-
Bunyaviridae RNA polymerases (L-protein) have an N-terminal, influenza-like endonuclease domain, essential for viral cap-dependent transcription.PLoS Pathog. 2010 Sep 16;6(9):e1001101. doi: 10.1371/journal.ppat.1001101. PLoS Pathog. 2010. PMID: 20862319 Free PMC article.
-
RNA-dependent activation of primer RNA production by influenza virus polymerase: different regions of the same protein subunit constitute the two required RNA-binding sites.EMBO J. 1998 Oct 1;17(19):5844-52. doi: 10.1093/emboj/17.19.5844. EMBO J. 1998. PMID: 9755184 Free PMC article.
-
Surprising function of the three influenza viral polymerase proteins: selective protection of viral mRNAs against the cap-snatching reaction catalyzed by the same polymerase proteins.Virology. 1996 Dec 15;226(2):430-5. doi: 10.1006/viro.1996.0673. Virology. 1996. PMID: 8955065
-
A multi-functional enzyme with RNA polymerase and RNase activities: molecular anatomy of influenza virus RNA polymerase.Biochimie. 1996;78(11-12):1097-102. doi: 10.1016/s0300-9084(97)86735-1. Biochimie. 1996. PMID: 9150890 Review.
-
Interplay between Influenza Virus and the Host RNA Polymerase II Transcriptional Machinery.Trends Microbiol. 2019 May;27(5):398-407. doi: 10.1016/j.tim.2018.12.013. Epub 2019 Jan 11. Trends Microbiol. 2019. PMID: 30642766 Free PMC article. Review.
Cited by
-
Temperature-sensitive lesions in two influenza A viruses defective for replicative transcription disrupt RNA binding by the nucleoprotein.J Virol. 1999 Sep;73(9):7349-56. doi: 10.1128/JVI.73.9.7349-7356.1999. J Virol. 1999. PMID: 10438824 Free PMC article.
-
The active sites of the influenza cap-dependent endonuclease are on different polymerase subunits.EMBO J. 2001 Apr 17;20(8):2078-86. doi: 10.1093/emboj/20.8.2078. EMBO J. 2001. PMID: 11296240 Free PMC article.
-
Attenuation of influenza A virus mRNA levels by promoter mutations.J Virol. 1998 Aug;72(8):6283-90. doi: 10.1128/JVI.72.8.6283-6290.1998. J Virol. 1998. PMID: 9658066 Free PMC article.
-
The active form of the influenza cap-snatching endonuclease inhibitor baloxavir marboxil is a tight binding inhibitor.J Biol Chem. 2021 Jan-Jun;296:100486. doi: 10.1016/j.jbc.2021.100486. Epub 2021 Feb 27. J Biol Chem. 2021. PMID: 33647314 Free PMC article.
-
The RNA polymerase of influenza a virus is stabilized by interaction with its viral RNA promoter.J Virol. 2002 Jul;76(14):7103-13. doi: 10.1128/jvi.76.14.7103-7113.2002. J Virol. 2002. PMID: 12072510 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous