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Role of a transductional-transcriptional processor complex involving MyD88 and IRF-7 in Toll-like receptor signaling
被引:398
作者:
Honda, K
Yanai, H
Mizutani, T
Negishi, H
Shimada, N
Suzuki, N
Ohba, Y
Takaoka, A
Yeh, WC
Taniguchi, T
机构:
[1] Univ Tokyo, Grad Sch Med, Dept Immunol, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Fac Med, Bunkyo Ku, Tokyo 1130033, Japan
[3] Univ Toronto, Hlth Network, Adv Med Discovery Inst, Dept Med Biophys, Toronto, ON M5G 2C1, Canada
[4] RIKEN, Res Ctr Allergy & Immunol, Tsurumi Ku, Yokohama, Kanagawa 230045, Japan
[5] Japan Sci & Technol Agcy, Precursory Res Embryon Sci & Technol, Informat & Cell Funct, Kawaguchi, Saitama 3320012, Japan
来源:
关键词:
D O I:
10.1073/pnas.0406933101
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Toll-like receptor (TLR) activation is central to immunity, wherein the activation of the TLR9 subfamily members TLR9 and TLR7 results in the robust induction of type I IFNs (IFN-alpha/beta) by means of the MyD88 adaptor protein. However, it remains unknown how the TLR signal "input" can be processed through MyD88 to "output" the induction of the IFN genes. Here, we demonstrate that the transcription factor IRF-7 interacts with MyD88 to form a complex in the cytoplasm. We provide evidence that this complex also involves IRAK4 and TRAF6 and provides the foundation for the TLR9-dependent activation of the IFN genes. The complex defined in this study represents an example of how the coupling of the signaling adaptor and effector kinase molecules together with the transcription factor regulate the processing of an extracellular signal to evoke its versatile downstream transcriptional events in a cell. Thus, we propose that this molecular complex may function as a cytoplasmic transductional-transcriptional processor.
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页码:15416 / 15421
页数:6
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