The goal of this Program of Excellence for Basic Research on AIDS is to understand at the molecular level the activation of Human Immunodeficiency Virus (HIV) from a state of latency to pathogenic expression. This understanding will be accomplished by an interdisciplinary approach involving studies in genetics, molecular and cell biology, biochemistry, and structural studies. The program is composed of seven individual sections: the Viral Genetics project will define the regulatory elements within the HIV promoter; the Signal Transduction project will define the signal transduction pathways in T cells responsible for HIV activation; the Cellular Transactivators project (Franza) will study the cellular transactivators involved in activation of the HIV promoter; the Viral Transactivators project will study the structure and function of the viral transactivator tat and its role in HIV activation; the Transcription project (Hernandez) will study the elements and cellular factors responsible for TAR function, which allow tat transactivation of HIV; the Transgenic Mice project will develop animal models to study the cis-acting HIV/LTR promoter elements and the effects of tat transactivation in vivo; the Structural Molecular Biology project will determine the X-ray crystallographic structures of both viral (tat) and (fos) transactivators of HIV gene expression. The structural studies form a cornerstone of this program as it is the interchange between functional studies and X-ray crystallographic studies that will guarantee the long-range success of this program and is most likely to lead to the rational design of drugs that will interfere with HIV activation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI027270-03
Application #
3091950
Study Section
Special Emphasis Panel (SRC (90))
Project Start
1988-09-01
Project End
1991-08-31
Budget Start
1990-09-01
Budget End
1991-08-31
Support Year
3
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Cold Spring Harbor Laboratory
Department
Type
DUNS #
065968786
City
Cold Spring Harbor
State
NY
Country
United States
Zip Code
11724
Skowronski, J; Parks, D; Mariani, R (1993) Altered T cell activation and development in transgenic mice expressing the HIV-1 nef gene. EMBO J 12:703-13
Laspia, M F; Wendel, P; Mathews, M B (1993) HIV-1 Tat overcomes inefficient transcriptional elongation in vitro. J Mol Biol 232:732-46
Echetebu, C O; Rice, A P (1993) Mutational analysis of the amino and carboxy termini of the HIV-2 Tat protein. J Acquir Immune Defic Syndr 6:550-7
Riabowol, K; Schiff, J; Gilman, M Z (1992) Transcription factor AP-1 activity is required for initiation of DNA synthesis and is lost during cellular aging. Proc Natl Acad Sci U S A 89:157-61
Kessler, M; Mathews, M B (1992) Premature termination and processing of human immunodeficiency virus type 1-promoted transcripts. J Virol 66:4488-96
Phares, W; Franza Jr, B R; Herr, W (1992) The kappa B enhancer motifs in human immunodeficiency virus type 1 and simian virus 40 recognize different binding activities in human Jurkat and H9 T cells: evidence for NF-kappa B-independent activation of the kappa B motif. J Virol 66:7490-8
Skowronski, J (1991) Expression of a human immunodeficiency virus type 1 long terminal repeat/simian virus 40 early region fusion gene in transgenic mice. J Virol 65:754-62
Li, Y C; Ross, J; Scheppler, J A et al. (1991) An in vitro transcription analysis of early responses of the human immunodeficiency virus type 1 long terminal repeat to different transcriptional activators. Mol Cell Biol 11:1883-93
Kessler, M; Mathews, M B (1991) Tat transactivation of the human immunodeficiency virus type 1 promoter is influenced by basal promoter activity and the simian virus 40 origin of DNA replication. Proc Natl Acad Sci U S A 88:10018-22
Graham, R; Gilman, M (1991) Distinct protein targets for signals acting at the c-fos serum response element. Science 251:189-92

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