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MOLECULAR-CLONING OF APRF, A NOVEL IFN-STIMULATED GENE FACTOR-3 P91-RELATED TRANSCRIPTION FACTOR INVOLVED IN THE GP130-MEDIATED SIGNALING PATHWAY
被引:901
作者:
AKIRA, S
NISHIO, Y
INOUE, M
WANG, XJ
WEI, S
MATSUSAKA, T
YOSHIDA, K
SUDO, T
NARUTO, M
KISHIMOTO, T
机构:
[1] TORAY INDUSTRIES LTD, BASIC RES LABS, KAMAKURA, KANAGAWA 248, JAPAN
[2] TORAY INDUSTRIES LTD, TORAY RES CTR, KAMAKURA, KANAGAWA 248, JAPAN
[3] OSAKA UNIV, SCH MED, DEPT MED 3, SUITA, OSAKA 565, JAPAN
来源:
关键词:
D O I:
10.1016/0092-8674(94)90235-6
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:
Acute-phase response factor (APRF) is a transcription factor that binds to the interleukin-6 (IL-6)-responsive elements identified in the promoters of various acute-phase protein genes. We report here the purification and cloning of APRF. APRF exhibits a 52.5% overall homology at the amino acid level with p91, a component of the interferon (IFN) stimulated gene factor 3 complexes. The cloned APRF protein is tyrosine phosphorylated and translocated into the nucleus in response to IL-6, but not in response to IFN-gamma. Tyrosine phosphorylation was also observed in response to other cytokines, such as leukemia inhibitory factor, oncostatin M, and ciliary neurotrophic factor, whose receptors share the IL-6 receptor signal transducer gp130. In contrast, we observed that p91. is not tyrosine phosphorylated in response to IL-6. These results suggest that this novel p91-related protein may play a major role in the gpl30-mediated signaling pathway and that selective activation of p91-related factors may explain the diversity of cellular responses to different cytokines.
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页码:63 / 71
页数:9
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