Stable TatIII cell lines, TatIII gene products, and assay methods
Abstract
Abstract This invention describes stable tatIII cell lines. It is disclosed that by transfecting a preselected tatIII cell line with a vector containing a sufficient amount of the HTLV-III LTR responsive to tatIII gene products for trans-activation and an enhancer upstream of the tatIII responsive segment, it is possible to express high levels of the tatIII gene products. By including a preselected heterologous gene on this vector, it is also possible to express high levels of a desired gene product. A substantially pure protein comprising 86 amino acids and having an apparent molecular weight of about 14,000 dalton and exhibiting trans-activating activity is also disclosed. This protein and polypeptides having trans-activating ability, which is also disclosed, can be used to produce high levels of a desired gene product. A method of detecting the presence of HTLV-III/LAV virus in an individual is also disclosed and comprises the step of: (a) incubating whole blood or lymphocytes from the invididual to be tested with tatIII cell lines of the present invention in a culture medium; and (b) screening for cytopathic effects on the cells is also disclosed. A method of screening for a compound that inhibits trans-activation of the tatIII gene product is also disclosed and comprises the steps of: (1) transacting a tatIII cell line of the present invention with a vector containing a gene that expresses a selectable marker and whose expression is under the control of an HTLV-III LTR; (2) transfecting the same type of tatIII cell lines as in step (1) with the selectable gene chosen in step (1) but under the control of a different regulatory sequence; (3) thereafter, adding a preselected compound to each of the cell lines in increasing concentrations; and (4) measuring the expression of the selectable gene product to determine whether the compound effects the tatIII function without being toxic to the cell.
Inventors
- 👤 William A. Haseltine
- 👤 Craig A. Rosen
- 👤 Joseph G. Sodroski
- 👤 Wei C. Goh
Bibliographic Details
Claims Analysis
Total Claims: 19References Cited (Backward Citations)
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