Subcellular localization of human immunodeficiency virus type 1 RNAs, Rev, and the splicing factor SC-35

被引:18
作者
Boe, SO [1 ]
Bjorndal, B [1 ]
Rosok, B [1 ]
Szilvay, AM [1 ]
Kalland, KH [1 ]
机构
[1] Univ Bergen, Bergen High Technol Ctr, Gade Inst, Dept Microbiol & Immunol,Ctr Res Virol, N-5020 Bergen, Norway
关键词
D O I
10.1006/viro.1998.9110
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The HIV-I protein Rev regulates the cytoplasmic levels of incompletely spliced HIV-1 mRNAs. The plasmid pSVc21, which contains a HIV-1 provirus, was introduced into COS cells by transient transfection. Simultaneous detection of HIV-1 RNAs and Rev proteins produced in transfected cells was then performed in order to determine the relative distribution of these two components. HIV-1 RNAs and the Rev protein localized to the same areas of the nucleoplasm, implying that these locations represent sites where Rev interacts with its target RNAs. Using a monoclonal antibody targeted to the splicing factor SC-35 it was demonstrated that the sites where HIV-1 mRNAs and Rev were detected often contained weak anti-SC-35 staining, whereas little RNA and Rev were found in strongly labeled SC-35-containing speckles. The same distribution of HIV-1 RNAs relative to SC-35 was also seen in transfected HeLa cells and in primary human lymphocytes infected with HIV-1 primary isolates. In addition, transiently expressed intron-containing beta-globin RMAs were shown to distribute to weak anti-SC-35 staining in a manner similar to that of HIV-1 RNAs. The findings suggest that Rev and HIV-1 RNAs interact at putative sites of mRNA transcription and splicing. (C) 1998 Academic Press.
引用
收藏
页码:473 / 482
页数:10
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