Herpes simplex virus gene expression is coordinately regulated and temporally controlled. The biosynthesis of early gene transcripts, eg the mRNA for thymidine kinase, is only catalyzed by host RNA polymerase after synthesis of functional immediate early gene products. When cloned immediate early gene are introduced into Hela cells along with a cloned tk gene, tk mRNA is faithfully transcribed. In the absence of immediate early gene sequences we detect little tk specific RNA. The experiments described in this grant application propose to use transient expression assays to define the immediate early genes that act in trans to activate transcription of tk gene. In other studies the sequences that code for the immediate early gene products will be modified in vitro and the effects of these mutations will be studied in a transient expression assay system.
Our aim i s to identify regulatory proteins, their functional domains and to determine if they interact with specific sequences in the virus chromosome.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA017477-15
Application #
3164718
Study Section
Virology Study Section (VR)
Project Start
1985-05-01
Project End
1990-04-30
Budget Start
1989-05-01
Budget End
1990-04-30
Support Year
15
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
Schools of Medicine
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10027
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