Proceedings of the National Academy of Sciences · 1985 · 168 citations · 35 references
Life SciencesMolecular BiologyOncologyMolecular OncologyMolecular VirologyVirologyOncogenic VirusesViral InfectionsViral OncogenesViral OncogenesisP21 RegulationTranscriptional ActivationTranscriptional Activation DomainsViral Open Reading FramesViral Protein LocalizationViral Tumor Antigens
Human T-cell leukemia virus type I (HTLV-I) is an etiological agent of adult T-cell leukemia and has a unique sequence, pX, that contains four possible open reading frames, I-IV. p40x was previously identified as the gene product of frame IV (x-lor) and was suggested to mediate transcriptional trans-activation of the viral long terminal repeats. We have identified two pX gene products, p27x-III and p21x-III, encoded by frame III, which mostly overlapped frame IV. These proteins were detected with rabbit antiserum against the synthetic peptide predicted from the 3' end of frame III. p27x-III is phosphorylated in cultured cells, and the phosphoprotein (pp27x-III) is localized in nuclei; some pp27x-III was tightly bound to nuclear components. p27x-III was detected in a number of cell lines that express other viral antigens, including a cell line previously reported to express only p40x as a viral protein. The function(s) of p27x-III and p21x-III is not known, but the tight binding of pp27x-III to nuclear components suggests that it is associated with regulation of viral gene expression.
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