Miyazaki Y, Takamatsu T, Nosaka T, Fujita S, Hatanaka M
Institute for Virus Research, Kyoto University, Japan.
FEBS Lett. 1992 Jun 22;305(1):1-5. doi: 10.1016/0014-5793(92)80642-t.
Subcellular localization of human immunodeficiency virus type I (HIV-1) Tat and Rev was examined using a confocal laser scanning microscope (CLSM). In transfected COS-7 cells, Tat resided exclusively in the perinocleolar region, while Rev infiltrated fully into the nucleoli. The chimeric Tat in which the nucleolar targeting signal was replaced by that of Rev, which retains trans-acting activity of Tat, remained still in the perinucleolar region as wild-type Tat. Perinucleolar distribution of Tat protein suggests the existence of a novel nucleolar architecture that affects transcription.
使用共聚焦激光扫描显微镜(CLSM)检测了人类免疫缺陷病毒I型(HIV-1)反式激活因子(Tat)和调节蛋白(Rev)的亚细胞定位。在转染的COS-7细胞中,Tat仅存在于核仁周围区域,而Rev则完全渗入核仁。嵌合Tat中核仁靶向信号被Rev的信号取代,该嵌合Tat保留了Tat的反式作用活性,其仍如野生型Tat一样停留在核仁周围区域。Tat蛋白的核仁周围分布表明存在一种影响转录的新型核仁结构。