Interaction between STAT-3 and HNF-3 leads to the activation of liver-specific hepatitis B virus enhancer 1 function

被引:68
作者
Waris, G
Siddiqui, A
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Microbiol, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Program Mol Biol, Denver, CO 80262 USA
关键词
D O I
10.1128/JVI.76.6.2721-2729.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The signal transducer and activator of transcription 3 (STAT-3), a member of the STAT family of proteins, binds to a large number of transcriptional control elements and regulates gene expression in response to cytokines. While it binds to its cognate nucleotide sequences, it has been recently shown to directly interact with other transcriptional factors in the absence of DNA. We report here one such novel interaction between STAT-3 and hepatocyte nuclear factor 3 (HNF-3) in the absence of DNA. We have identified a STAT-3 binding site within the core domain of hepatitis B virus (HBV) enhancer 1. The HBV enhancer I DNA-STAT-3 protein interaction is shown to be stimulated by interleukin-6 (IL-6) and epidermal growth factor, which leads to an overall stimulation of HBV enhancer I function and viral gene expression. Using mobility shift assays and transient transfection schemes, we demonstrate a cooperative interaction between HNF-3 and STAT-3 in mediating the cytokine-mediated HBV enhancer function. Cytokine stimulation of HBV gene expression represents an important regulatory scheme of direct relevance to liver disease pathogenesis associated with HBV infection.
引用
收藏
页码:2721 / 2729
页数:9
相关论文
共 56 条
[31]   ASSOCIATION OF TRANSCRIPTION FACTOR APRF AND PROTEIN-KINASE JAK1 WITH THE INTERLEUKIN-6 SIGNAL TRANSDUCER GP130 [J].
LUTTICKEN, C ;
WEGENKA, UM ;
YUAN, JP ;
BUSCHMANN, J ;
SCHINDLER, C ;
ZIEMIECKI, A ;
HARPUR, AG ;
WILKS, AF ;
YASUKAWA, K ;
TAGA, T ;
KISHIMOTO, T ;
BARBIERI, G ;
PELLEGRINI, S ;
SENDTNER, M ;
HEINRICH, PC ;
HORN, F .
SCIENCE, 1994, 263 (5143) :89-92
[32]  
MIRKOVITCH J, 1992, MOL CELL BIOL, V12, P1
[33]   A central role for Stat3 in IL-6-induced regulation of growth and differentiation in M1 leukemia cells [J].
Nakajima, K ;
Yamanaka, Y ;
Nakae, K ;
Kojima, H ;
Ichiba, M ;
Kiuchi, N ;
Kitaoka, T ;
Fukada, T ;
Hibi, M ;
Hirano, T .
EMBO JOURNAL, 1996, 15 (14) :3651-3658
[34]  
Ohno H, 1997, J MED VIROL, V52, P413, DOI 10.1002/(SICI)1096-9071(199708)52:4<413::AID-JMV12>3.0.CO
[35]  
2-H
[36]   INTERACTIONS BETWEEN NUCLEAR FACTORS AND THE HEPATITIS-B VIRUS ENHANCER [J].
PATEL, NU ;
JAMEEL, S ;
ISOM, H ;
SIDDIQUI, A .
JOURNAL OF VIROLOGY, 1989, 63 (12) :5293-5301
[37]   Stat protein transactivation domains recruit p300/CBP through widely divergent sequences [J].
Paulson, M ;
Pisharody, S ;
Pan, L ;
Guadagno, S ;
Mui, AL ;
Levy, DE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (36) :25343-25349
[38]  
REINHOLD W, 1995, MOL CELL BIOL, V15, P3041
[39]   REGULATION OF C-FOS EXPRESSION IN TRANSGENIC MICE REQUIRES MULTIPLE INTERDEPENDENT TRANSCRIPTION CONTROL ELEMENTS [J].
ROBERTSON, LM ;
KERPPOLA, TK ;
VENDRELL, M ;
LUK, D ;
SMEYNE, RJ ;
BOCCHIARO, C ;
MORGAN, JI ;
CURRAN, T .
NEURON, 1995, 14 (02) :241-252
[40]   A COMMON NUCLEAR SIGNAL-TRANSDUCTION PATHWAY ACTIVATED BY GROWTH-FACTOR AND CYTOKINE RECEPTORS [J].
SADOWSKI, HB ;
SHUAI, K ;
DARNELL, JE ;
GILMAN, MZ .
SCIENCE, 1993, 261 (5129) :1739-1744