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Adenosine deaminase is a specific partner for the Grb2 isoform Grb3-3.

Authors :
Ramos-Morales F
Domínguez A
Rios RM
Barroso SI
Infante C
Schweighoffer F
Tocqué B
Pintor-Toro JA
Tortolero M
Source :
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 1997 Aug 28; Vol. 237 (3), pp. 735-40.
Publication Year :
1997

Abstract

Grb3-3 is an isoform of Grb2, thought to arise by alternative splicing, that lacks a functional SH2 domain but retains functional SH3 domains, which allow interaction with other proteins through binding to prolinerich sequences. Several evidences suggest that besides common partners for Grb2 and Grb3-3, specific targets could exist. In order to find specific partners for Grb3-3, we have screened a human cDNA library by the yeast two-hybrid system with Grb3-3 as a bait. We have identified adenosine deaminase, an enzyme involved in purine metabolism whose deficiency is associated with severe combined immunodeficiency, as a Grb3-3 binding protein that is not able to bind to Grb2. This interaction has been confirmed in vitro with GST fusion proteins and in vivo by coimmunoprecipitation experiments in NIH3T3 cells stably transfected with Grb3-3. The functional significance of this finding is discussed.

Details

Language :
English
ISSN :
0006-291X
Volume :
237
Issue :
3
Database :
MEDLINE
Journal :
Biochemical and biophysical research communications
Publication Type :
Academic Journal
Accession number :
9299436
Full Text :
https://doi.org/10.1006/bbrc.1997.7221