Yamagoe S, Kohda T, Oishi M
Institute of Applied Microbiology, University of Tokyo, Japan.
Mol Cell Biol. 1991 Jul;11(7):3522-7. doi: 10.1128/mcb.11.7.3522-3527.1991.
Gene expression of human immunodeficiency virus type 1 (HIV-1) is induced not only by trans activation mediated through a gene product (tat) encoded by the virus but also by treatment of virus-carrying cells with DNA-damaging agents such as UV light. Employing an artificially constructed DNA in which the chloramphenicol acetyltransferase gene was placed under the control of the HIV-1 long terminal repeat, we analyzed the induction process in HeLa cells and found that inhibitors of poly(ADP-ribose) polymerase suppressed UV-induced HIV-1 gene expression but not tat-mediated expression. We also found that suppression occurs at the posttranscriptional level. These results indicate that HIV-1 gene expression is activated by at least two different mechanisms, one of which involves poly-ADP ribosylation. A possible new role of poly-ADP ribosylation in the regulation of specific gene expression is also discussed.
1型人类免疫缺陷病毒(HIV-1)的基因表达不仅由病毒编码的基因产物(tat)介导的反式激活所诱导,还可由用紫外线等DNA损伤剂处理携带病毒的细胞所诱导。利用人工构建的DNA,其中氯霉素乙酰转移酶基因置于HIV-1长末端重复序列的控制之下,我们分析了HeLa细胞中的诱导过程,发现聚(ADP-核糖)聚合酶抑制剂可抑制紫外线诱导的HIV-1基因表达,但不抑制tat介导的表达。我们还发现抑制发生在转录后水平。这些结果表明,HIV-1基因表达至少由两种不同机制激活,其中一种涉及多聚ADP核糖基化。还讨论了多聚ADP核糖基化在特定基因表达调控中的可能新作用。