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Transcriptional and post-transcriptional controls establish the cascade of herpes simplex virus protein synthesis.

作者信息

Weinheimer S P, McKnight S L

机构信息

Carnegie Institution of Washington, Department of Embryology, Baltimore, MD 21210.

出版信息

J Mol Biol. 1987 Jun 20;195(4):819-33. doi: 10.1016/0022-2836(87)90487-6.

DOI:10.1016/0022-2836(87)90487-6
PMID:2821283
Abstract

Gene expression by herpes simplex virus type 1 (HSV-1) results in the synthesis of three temporal classes of viral proteins. The three classes of viral proteins are expressed in a cascade manner of sequential dependency. The molecular mechanisms that account for the HSV-1 protein synthesis cascade are poorly understood. In order to provide a detailed description of the metabolic levels at which HSV-1 protein synthesis is regulated, we have measured transcription rates and mRNA accumulation levels for 11 HSV-1 genes. These measurements were made over a time-course of infection in the presence or absence of metabolic inhibitors of either viral protein synthesis or viral DNA synthesis. Our observations show that the protein synthesis cascade of HSV-1 is established as a consequence of mechanisms that regulate both the transcription and accumulation of viral messenger RNA.

摘要

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