INVOLVEMENT OF CRAF1, A RELATIVE OF TRAF, IN CD40 SIGNALING

被引:433
作者
CHENG, GH
CLEARY, AM
YE, ZS
HONG, DI
LEDERMAN, S
BALTIMORE, D
机构
[1] MIT, DEPT BIOL, CAMBRIDGE, MA 02139 USA
[2] COLUMBIA UNIV, DEPT MED, NEW YORK, NY 10032 USA
[3] ROCKEFELLER UNIV, NEW YORK, NY 10021 USA
关键词
D O I
10.1126/science.7533327
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
CD40 is a receptor on the surface of B lymphocytes, the activation of which leads to B cell survival, growth, and differentiation. A yeast two-hybrid screen identified a gene, CRAF1, encoding a protein that interacts directly with the CD40 cytoplasmic tail through a region of similarity to the tumor necrosis factor-alpha (TNF-alpha) receptor-associated factors. Overexpression of a truncated CRAF1 gene inhibited CD40-mediated up-regulation of CD23. A region of CRAF1 was similar to the TNF-alpha receptor-associated factors TRAF1 and TRAF2 and so defined a shared TRAF-C domain that was necessary and sufficient for CD40 binding and homodimerization. The CRAF1 sequence also predicted a long amphipathic helix, a pattern of five zinc fingers, and a zinc ring finger. It is likely that other members of the TNF receptor superfamily use CRAF-related proteins in their signal transduction processes.
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页码:1494 / 1498
页数:5
相关论文
共 51 条
[51]  
YELLIN MJ, 1994, J IMMUNOL, V153, P666