Inoue J, Itoh M, Akizawa T, Toyoshima H, Yoshida M
Department of Viral Oncology, Cancer Institute, Tokyo, Japan.
Oncogene. 1991 Oct;6(10):1753-7.
The Rex protein of human T-cell leukemia viruses (HTLV) is a trans-acting regulator inducing the expression of gag and env mRNA containing the introns. The rex gene can also induce expression of unspliced RNA of human immunodeficiency viruses (HIV). We have analyzed the level of spliced and unspliced RNAs in nucleus and cytoplasm to understand the mechanism by which the Rex protein modulates RNA processing. With the gag gene of HTLV-1, the unspliced RNA was accumulated by Rex protein in both nucleus and cytoplasm. However, the apparent effects on nuclear unspliced RNA depended on the reporter genes: with the env gene of HTLV-1 as well as that of HIV-1, Rex did not accumulate the unspliced RNA in nucleus, but did so only in cytoplasm. These results clearly indicate that Rex protein not only activates the nuclear export of unspliced RNA, but also modulates some steps of RNA processing before the splicing, probably through stabilization of the precursor RNA.
人类T细胞白血病病毒(HTLV)的Rex蛋白是一种反式作用调节因子,可诱导含有内含子的gag和env mRNA的表达。rex基因还可诱导人类免疫缺陷病毒(HIV)未剪接RNA的表达。我们分析了细胞核和细胞质中剪接和未剪接RNA的水平,以了解Rex蛋白调节RNA加工的机制。对于HTLV-1的gag基因,未剪接的RNA在细胞核和细胞质中均被Rex蛋白积累。然而,对细胞核中未剪接RNA的明显影响取决于报告基因:对于HTLV-1的env基因以及HIV-1的env基因,Rex并未在细胞核中积累未剪接的RNA,而仅在细胞质中积累。这些结果清楚地表明,Rex蛋白不仅激活未剪接RNA的核输出,还可能通过稳定前体RNA来调节剪接前RNA加工的某些步骤。