Michienzi A, Cagnon L, Bahner I, Rossi J J
Department of Molecular Biology, Beckman Research Institute of the City of Hope, and Graduate School of Biological Sciences, City of Hope, Duarte, CA 91010-3011, USA.
Proc Natl Acad Sci U S A. 2000 Aug 1;97(16):8955-60. doi: 10.1073/pnas.97.16.8955.
The HIV regulatory proteins Tat and Rev have a nucleolar localization property in human cells. However, no functional role has been attributed to this localization. Recently it has been demonstrated that expression of Rev induces nucleolar relocalization of some protein factors involved in Rev export. Because the function of Rev is to bind HIV RNA and facilitate transport of singly spliced and unspliced RNA to the cytoplasm, it is likely that the nucleolus plays a critical role in HIV-1 RNA export. As a test for trafficking of HIV-1 RNAs into the nucleolus, a hammerhead ribozyme that specifically cleaves HIV-1 RNA was inserted into the body of the U16 small nucleolar RNA, resulting in accumulation of the ribozyme within the nucleoli of human cells. HeLa CD4(+) and T cells expressing this nucleolar localized ribozyme exhibit dramatically suppressed HIV-1 replication. The results presented here suggest a trafficking of HIV-1 RNA through the nucleoli of human cells, thus posing a different paradigm for lentiviral RNA processing.
HIV调节蛋白Tat和Rev在人类细胞中具有核仁定位特性。然而,这种定位尚未被赋予任何功能作用。最近有研究表明,Rev的表达会诱导一些参与Rev输出的蛋白质因子重新定位于核仁。由于Rev的功能是结合HIV RNA并促进单剪接和未剪接RNA向细胞质的转运,因此核仁很可能在HIV-1 RNA输出中起关键作用。作为对HIV-1 RNA进入核仁运输的一种检测,一种特异性切割HIV-1 RNA的锤头状核酶被插入到U16小核仁RNA体内,导致核酶在人类细胞核仁中积累。表达这种核仁定位核酶的HeLa CD4(+)细胞和T细胞表现出HIV-1复制的显著抑制。此处呈现的结果表明HIV-1 RNA通过人类细胞核仁进行运输,从而为慢病毒RNA加工提出了一种不同的模式。