共 2 条
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
相关论文