Translational requirement for La Crosse virus S-mRNA synthesis: a possible mechanism

Author:

Bellocq C1,Kolakofsky D1

Affiliation:

1. Department of Microbiology, University of Geneva Medical School, Switzerland.

Abstract

Ongoing protein synthesis is required for La Crosse S-mRNA synthesis in vivo, and complete S-mRNA can be made in vitro only in the presence of an active rabbit reticulocyte lysate. Using in vitro systems based on the polymerase activity of purified virions, we further support the notion that it is translation of the nascent mRNA that is required for complete transcription. Since replacement of guanosine with inosine in the nascent mRNA substitutes for the translational requirement, it appears that translation is required to prevent interactions of the nascent chain from taking place, which, if not prevented, lead to premature termination. These interactions appear to be between the nascent mRNA chain and its nucleocapsid template. A model for the translational requirement for complete S-mRNA synthesis is presented.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference20 articles.

1. Early RNA synthesis in Bunyawera virus-infected cells;Abraham G.;J. Gen. Virol.,1983

2. Translational requirement of La Crosse virus S-mRNA synthesis: in vitro studies;Bellocq C.;J. Virol.,1987

3. Nonviral heterogeneous sequences are present at the 5' ends of one species of snowshoe hare bunyavirus S complementary RNA;Bishop D. H. L.;Nucleic Acids Res.,1983

4. Use of complementary DNA oligomers to probe trp leader transcript secondary structures involved in transcription pausing and termination;Fischer R.;Nucleic Acids Res.,1984

5. Gerbaud S. N. Pardigon P. Vialat and M. Bouloy. 1987. In D. Kolakofsky and B. W. J. Mahy (ed.) Biology of negative strand viruses. Elsevier Biomedical Press Amsterdam.

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