Fridell R A, Fischer U, Lührmann R, Meyer B E, Meinkoth J L, Malim M H, Cullen B R
Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710, USA.
Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):2936-40. doi: 10.1073/pnas.93.7.2936.
The human immunodeficiency virus type 1 (HIV-1) Rev protein is required for nuclear export of late HIV-1 mRNAs. This function is dependent on the mutationally defined Rev activation domain, which also forms a potent nuclear export signal. Transcription factor IIIA (TFIIIA) binds to 5S rRNA transcripts and this interaction has been proposed to play a role in the efficient nuclear export of 5S rRNA in amphibian oocytes. Here it is reported that amphibian TFIIIA proteins contain a sequence element with homology to the Rev activation domain that effectively substitutes for this domain in inducing the nuclear export of late HIV-1 mRNAs. It is further demonstrated that this TFIIIA sequence element functions as a protein nuclear export signal in both human cells and frog oocytes. Thus, this shared protein motif may play an analogous role in mediating the nuclear export of both late HIV-1 RNAs and 5S rRNA transcripts.
1型人类免疫缺陷病毒(HIV-1)的Rev蛋白是HIV-1晚期mRNA核输出所必需的。该功能依赖于经突变定义的Rev激活结构域,该结构域同时也构成一个有效的核输出信号。转录因子IIIA(TFIIIA)与5S rRNA转录本结合,有人提出这种相互作用在两栖类卵母细胞中5S rRNA的有效核输出中发挥作用。本文报道,两栖类TFIIIA蛋白含有一个与Rev激活结构域具有同源性的序列元件,该元件在诱导HIV-1晚期mRNA核输出方面可有效替代该结构域。进一步证明,该TFIIIA序列元件在人类细胞和蛙卵母细胞中均作为一种蛋白质核输出信号发挥作用。因此,这种共享的蛋白质基序可能在介导HIV-1晚期RNA和5S rRNA转录本的核输出中发挥类似作用。