Cited by 698

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

Takayama, Shinichi, Sato, Takaaki, Krajewski, Stanislaw, Kochel, Kristine, Irie, Shinji, Milian, Juan A, Reed, John C·1995·Cell

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.

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Crossref · 10.1016/0092-8674(95)90410-7

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  • BAG-1 interacts with Hsp70 family of molecular chaperones, displaying cytoprotective activities and effects on signal transduction and transcription, suggesting a function in overcoming cellular stress and inflammation.

    “BAG-1 is known to interact with heat shock protein 70 (Hsp70) family of molecular chaperones, displaying a variety of cytoprotective activities and effects on signal transduction and transcription, suggesting a function in overcoming cellular stress and inflammation38,39.”

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Authors
Takayama, S., Sato, T., Krajewski, S., Kochel, K., Irie, S., Milian, J. A., & Reed, J. C.
Venue
Cell
Publisher
Elsevier BV
Published
1995-01
Volume
80
Issue
2
Pages
279-284
ISSN
0092-8674
Cited by
698
References
0
Language
en

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