Hepatitis C virus NS5A protein modulates transcription through a novel cellular transcription factor SRCAP

被引:72
作者
Ghosh, AK
Majumder, M
Steele, R
Yaciuk, P
Chrivia, J
Ray, R
Ray, RB
机构
[1] St Louis Univ, Dept Pathol, St Louis, MO 63104 USA
[2] St Louis Univ, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
[3] St Louis Univ, Dept Pharmacol & Physiol Sci, St Louis, MO 63104 USA
[4] St Louis Univ, Div Infect Dis & Immunol, St Louis, MO 63104 USA
关键词
D O I
10.1074/jbc.275.10.7184
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
Hepatitis C virus NS5A protein transcriptionally modulates cellular genes and promotes cell growth. NS5A is likely to exert its activity in concert with cellular factor(s), Using a yeast two-hybrid screen, we have demonstrated that NS5A interacts with the C-terminal end of a newly identified cellular transcription factor, SRCAP, The authenticity of this interaction was verified by a mammalian two-hybrid assay, in vitro pull-down experiment, and an in vivo coimmunoprecipitation assay in human hepatoma (HepG2) cells. An in vitro transient transfection assay demonstrated that SRCAP can efficiently activate transcription when recruited by the Gal4 DNA-binding domain to the promoter. However, down-regulation of p21 promoter activity by NS5A was enhanced following ectopic expression of SRCAP, Together these results suggest that the interaction of NS5A and SRCAP may be one of the mechanisms by which NS5A exerts its effect on cell growth regulation contributing to hepatitis C virus-mediated pathogenesis.
引用
收藏
页码:7184 / 7188
页数:5
相关论文
共 29 条
  • [1] Hepatitis C and hepatocellular carcinoma
    DiBisceglie, AM
    [J]. HEPATOLOGY, 1997, 26 (03) : S34 - S38
  • [2] WAF1, A POTENTIAL MEDIATOR OF P53 TUMOR SUPPRESSION
    ELDEIRY, WS
    TOKINO, T
    VELCULESCU, VE
    LEVY, DB
    PARSONS, R
    TRENT, JM
    LIN, D
    MERCER, WE
    KINZLER, KW
    VOGELSTEIN, B
    [J]. CELL, 1993, 75 (04) : 817 - 825
  • [3] Antiapoptotic and oncogenic potentials of hepatitis C virus are linked to interferon resistance by viral repression of the PKR protein kinase
    Gale, M
    Kwieciszewski, B
    Dossett, M
    Nakao, H
    Katze, MG
    [J]. JOURNAL OF VIROLOGY, 1999, 73 (08) : 6506 - 6516
  • [4] Hepatitis C virus NS5A protein modulates cell cycle regulatory genes and promotes cell growth
    Ghosh, AK
    Steele, R
    Meyer, K
    Ray, R
    Ray, RB
    [J]. JOURNAL OF GENERAL VIROLOGY, 1999, 80 : 1179 - 1183
  • [5] PTEN transcriptionally modulates c-myc gene expression in human breast carcinoma cells and is involved in cell growth regulation
    Ghosh, AK
    Grigorieva, I
    Steele, R
    Hoover, RG
    Ray, RB
    [J]. GENE, 1999, 235 (1-2) : 85 - 91
  • [6] MBP-1 physically associates with histone deacetylase for transcriptional repression
    Ghosh, AK
    Steele, R
    Ray, RB
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 260 (02) : 405 - 409
  • [7] EXPRESSION AND IDENTIFICATION OF HEPATITIS C VIRUS POLYPROTEIN CLEAVAGE PRODUCTS
    GRAKOUI, A
    WYCHOWSKI, C
    LIN, C
    FEINSTONE, SM
    RICE, CM
    [J]. JOURNAL OF VIROLOGY, 1993, 67 (03) : 1385 - 1395
  • [8] HARPER JW, 1993, CELL, V75, P805
  • [9] Phosphorylation of nonstructural 5A protein of hepatitis C virus: HCV group-specific hyperphosphorylation
    Hirota, M
    Satoh, S
    Asabe, S
    Kohara, M
    Tsukiyama-Kohara, K
    Kato, N
    Hijikata, M
    Shimotohno, K
    [J]. VIROLOGY, 1999, 257 (01) : 130 - 137
  • [10] Hepatitis C virus NS5A protein is phosphorylated in vitro by a stably bound protein kinase from HeLa cells and by cAMP-dependent protein kinase A-α catalytic subunit
    Ide, Y
    Tanimoto, A
    Sasaguri, Y
    Padmanabhan, R
    [J]. GENE, 1997, 201 (1-2) : 151 - 158