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Fas(Apo-1/CD95)与泛素化途径相关蛋白的相互作用。

Interaction of Fas(Apo-1/CD95) with proteins implicated in the ubiquitination pathway.

作者信息

Becker K, Schneider P, Hofmann K, Mattmann C, Tschopp J

机构信息

Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland.

出版信息

FEBS Lett. 1997 Jul 21;412(1):102-6. doi: 10.1016/s0014-5793(97)00758-8.

Abstract

Fas(Apo-1/CD95), a receptor belonging to the tumor necrosis factor receptor family, induces apoptosis when triggered by Fas ligand. Upon its activation, the cytoplasmic domain of Fas binds several proteins which transmit the death signal. We used the yeast two-hybrid screen to isolate Fas-associated proteins. Here we report that the ubiquitin-conjugating enzyme UBC9 binds to Fas at the interface between the death domain and the membrane-proximal region of Fas. This interaction is also seen in vivo. UBC9 transiently expressed in HeLa cells bound to the co-expressed cytoplasmic segment of Fas. FAF1, a Fas-associated protein that potentiates apoptosis (Chu et al. (1996) Proc. Natl. Acad. Sci. USA 92, 11894-11898), was found to contain sequences similar to ubiquitin. These results suggest that proteins related to the ubiquitination pathway may modulate the Fas signaling pathway.

摘要

Fas(Apo-1/CD95)是一种属于肿瘤坏死因子受体家族的受体,当被Fas配体触发时可诱导细胞凋亡。激活后,Fas的胞质结构域会结合几种传递死亡信号的蛋白质。我们利用酵母双杂交筛选来分离Fas相关蛋白。在此我们报告泛素结合酶UBC9在Fas的死亡结构域与膜近端区域之间的界面处与Fas结合。这种相互作用在体内也能观察到。在HeLa细胞中瞬时表达的UBC9与共表达的Fas胞质片段结合。FAF1是一种增强细胞凋亡的Fas相关蛋白(Chu等人,(1996年)《美国国家科学院院刊》92,11894 - 11898),被发现含有与泛素相似的序列。这些结果表明,与泛素化途径相关的蛋白质可能会调节Fas信号通路。

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