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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.
Tranell, Anna; Fenyö, Eva Maria; Schwartz, Stefan.
Afiliação
  • Tranell A; Department of Medical Biochemistry & Microbiology Biomedical Center, BMC, Uppsala University, 75123 Uppsala, Sweden.
J Biol Chem ; 285(41): 31537-47, 2010 Oct 08.
Article em En | MEDLINE | ID: mdl-20685659
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfoproteínas / RNA Mensageiro / RNA Viral / Proteínas Nucleares / Éxons / HIV-1 / Proteínas de Ligação a RNA / Processamento Alternativo / Sítios de Splice de RNA / Produtos do Gene vpr do Vírus da Imunodeficiência Humana Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Biol Chem Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Suécia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfoproteínas / RNA Mensageiro / RNA Viral / Proteínas Nucleares / Éxons / HIV-1 / Proteínas de Ligação a RNA / Processamento Alternativo / Sítios de Splice de RNA / Produtos do Gene vpr do Vírus da Imunodeficiência Humana Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Biol Chem Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Suécia