Malim M H, Tiley L S, McCarn D F, Rusche J R, Hauber J, Cullen B R
Howard Hughes Medical Institute, Department of Microbiology and Immunology, Duke University Medical Center, Durham, North Carolina 27710.
Cell. 1990 Feb 23;60(4):675-83. doi: 10.1016/0092-8674(90)90670-a.
Expression of human immunodeficiency virus type 1 structural proteins requires both the viral Rev trans-activator and its cis-acting RNA target sequence, the Rev response element (RRE). The RRE has been mapped to a conserved region of the HIV-1 env gene and is predicted to form a complex, highly stable RNA stem-loop structure. Site-directed mutagenesis was used to define a small subdomain of the RRE, termed stem-loop II, that is essential for biological activity. Gel retardation assays demonstrated that the Rev trans-activator is a sequence-specific RNA binding protein. The RRE stem-loop II subdomain was found to be both necessary and sufficient for the binding of Rev by the RRE. We propose that the HIV-1 Rev trans-activator belongs to a new class of sequence-specific RNA binding proteins characterized by the presence of an arginine-rich binding motif.
1型人类免疫缺陷病毒结构蛋白的表达既需要病毒Rev反式激活因子,也需要其顺式作用RNA靶序列,即Rev反应元件(RRE)。RRE已被定位到HIV-1 env基因的一个保守区域,并预计形成一个复杂、高度稳定的RNA茎环结构。采用定点诱变来确定RRE的一个小亚结构域,称为茎环II,它对生物活性至关重要。凝胶阻滞试验表明,Rev反式激活因子是一种序列特异性RNA结合蛋白。发现RRE茎环II亚结构域对于RRE与Rev的结合既是必要的也是充分的。我们提出,HIV-1 Rev反式激活因子属于一类新的序列特异性RNA结合蛋白,其特征是存在富含精氨酸的结合基序。