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BAG-1的克隆与功能分析:一种具有抗细胞死亡活性的新型Bcl-2结合蛋白

Cloning and functional analysis of BAG-1: a novel Bcl-2-binding protein with anti-cell death activity.

作者信息

Takayama S, Sato T, Krajewski S, Kochel K, Irie S, Millan J A, Reed J C

机构信息

La Jolla Cancer Research Foundation, California 92037.

出版信息

Cell. 1995 Jan 27;80(2):279-84. doi: 10.1016/0092-8674(95)90410-7.

Abstract

Using a protein interaction cloning technique, we identified cDNAs that encode a novel Bcl-2-binding protein, termed BAG-1. The BAG-1 protein shares no significant homology with Bcl-2 or other Bcl-2 family proteins, which can form homo- and heterodimers. In gene transfer experiments using a human lymphoid cell line, Jurkat, coexpression of BAG-1 and Bcl-2 provided markedly increased protection from cell death induced by several stimuli, including staurosporine, anti-Fas antibody, and cytolytic T cells, relative to cells that contained gene transfer-mediated elevations in either BAG-1 or Bcl-2 protein alone. BAG-transfected 3T3 fibroblasts also exhibited prolonged cell survival in response to an apoptotic stimulus. The findings indicate that bag-1 represents a new type of anti-cell death gene and suggest that some routes of apoptosis induction previously ascribed to Bcl-2-independent pathways may instead reflect a need for the combination of Bcl-2 and BAG-1.

摘要

我们运用蛋白质相互作用克隆技术,鉴定出了编码一种新型Bcl-2结合蛋白(称为BAG-1)的cDNA。BAG-1蛋白与Bcl-2或其他能形成同二聚体和异二聚体的Bcl-2家族蛋白没有显著同源性。在使用人类淋巴细胞系Jurkat进行的基因转移实验中,与单独含有基因转移介导的BAG-1或Bcl-2蛋白升高的细胞相比,BAG-1和Bcl-2的共表达对包括星形孢菌素、抗Fas抗体和细胞毒性T细胞在内的多种刺激诱导的细胞死亡提供了显著增强的保护作用。BAG转染的3T3成纤维细胞对凋亡刺激也表现出延长的细胞存活。这些发现表明bag-1代表一种新型的抗细胞死亡基因,并提示一些先前归因于Bcl-2非依赖性途径的凋亡诱导途径可能反而反映了对Bcl-2和BAG-1组合的需求。

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