Hauber J, Malim M H, Cullen B R
Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710.
J Virol. 1989 Mar;63(3):1181-7. doi: 10.1128/JVI.63.3.1181-1187.1989.
The tat trans-activators encoded by the known strains of primate immunodeficiency virus share a conserved, highly basic protein domain. Mutagenesis of this sequence in the tat gene of human immunodeficiency virus type 1 is shown here to reduce, but not eliminate, the trans-activation of human immunodeficiency virus type 1-specific gene expression. The degree of inhibition is shown to vary in a dose-dependent manner and is most marked at low levels of tat expression. Multiple mutations of the basic domain of tat were found to impair both the in vivo stability and the nuclear localization of the tat protein. It is proposed that this protein domain serves to efficiently target the tat gene product to its appropriate site or substrate within the nucleus of expressing cells.
灵长类免疫缺陷病毒已知毒株编码的反式激活因子tat共享一个保守的、高度碱性的蛋白质结构域。本文显示,对人类免疫缺陷病毒1型tat基因中的该序列进行诱变可降低但不能消除人类免疫缺陷病毒1型特异性基因表达的反式激活作用。抑制程度呈剂量依赖性变化,在低水平tat表达时最为明显。发现tat碱性结构域的多个突变会损害tat蛋白的体内稳定性和核定位。有人提出,该蛋白质结构域有助于将tat基因产物有效地靶向到表达细胞细胞核内的适当位点或底物上。