Serine- and Arginine-rich Proteins 55 and 75 (SRp55 and SRp75) Induce Production of HIV-1 vpr mRNA by Inhibiting the 5′-Splice Site of Exon 3

被引:21
|
作者
Tranell, Anna [1 ]
Fenyo, Eva Maria [2 ]
Schwartz, Stefan [1 ,3 ]
机构
[1] Uppsala Univ, Dept Med Biochem & Microbiol, Biomed Ctr, BMC, S-75123 Uppsala, Sweden
[2] Lund Univ, Dept Lab Med, S-22362 Lund, Sweden
[3] Dublin Inst Technol, Dublin 8, Ireland
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; HUMAN-PAPILLOMAVIRUS TYPE-16; SPLICING FACTOR SF2/ASF; GENE-EXPRESSION; TAT EXON-2; HNRNP A1; UNTRANSLATED REGION; FUNCTIONAL-ANALYSIS; SILENCER ELEMENT/; EPITHELIAL-CELLS;
D O I
10.1074/jbc.M109.077453
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
HIV-1 non-coding exon 3 can either be spliced to exons 4, 4a, 4b, 4c, and 5 to generate tat, rev, and nef mRNAs or remain unspliced to produce the 13a7 vpr mRNA. Here we show that serine-and arginine-rich proteins 55 and 75 (SRp55 and SRp75) inhibit splicing from the 5'-splice site of exon 3 thereby causing an accumulation of the partially unspliced 13a7 vpr mRNA. In contrast, serine- and arginine-rich protein 40 (SRp40) induces splicing from exon 3 to exon 4, thereby promoting the production of the 1347 tat mRNA. We demonstrate that SRp55 stimulates vpr mRNA production by interacting with the previously identified HIV-1 splicing enhancer named GAR and inhibiting its function. This inhibition requires both serine arginine-rich and RNA-binding domains of SRp55, indicating that production of HIV-1 vpr mRNA depends on the interaction of SRp55 with an unknown factor.
引用
收藏
页码:31537 / 31547
页数:11
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