Proteins interacting with Caenorhabditis elegans Gα subunits

被引:30
作者
Cuppen, E
van der Linden, AM
Jansen, G
Plasterk, RHA
机构
[1] Hubrecht Lab, NL-3584 CT Utrecht, Netherlands
[2] Erasmus Univ, Ctr Med, MGC, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
[3] Erasmus Univ, Ctr Med, Ctr Biomed Genet, NL-3000 DR Rotterdam, Netherlands
来源
COMPARATIVE AND FUNCTIONAL GENOMICS | 2003年 / 4卷 / 05期
关键词
heterotrimeric G-protein; signal transduction; protein interaction; nuclear receptor; FUNCTIONAL GENOMIC ANALYSIS; GENE; NEMATODE; INTERFERENCE; MUTATIONS; G(O)ALPHA; G(Q)ALPHA; PROTEOME; FAMILY; YEAST;
D O I
10.1002/cfg.318
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To identify novel components in heterotrimeric G-protein signalling, we performed an extensive screen for proteins interacting with Caenorhabditis elegans Galpha subunits. The genome of C. elegans contains homologues of each of the four mammalian classes of Galpha subunits (Gs, Gi/o, Gq and G12), and 17 other Galpha subunits. We tested 19 of the Galpha subunits and four constitutively activated Galpha subunits in a large-scale yeast two-hybrid experiment. This resulted in the identification of 24 clones, representing 11 different proteins that interact with four different Galpha subunits. This set includes C. elegans orthologues of known interactors of Galpha subunits, such as AGS3 (LGN/PINS), CalNuc and Rap1Gap, but also novel proteins, including two members of the nuclear receptor super family and a homologue of human haspin (germ cell-specific kinase). All interactions were found to be unique for a specific Galpha subunit but variable for the activation status of the Galpha subunit. We used expression pattern and RNA interference analysis of the G-protein interactors in an attempt to substantiate the biological relevance of the observed interactions. Furthermore, by means of a membrane recruitment assay, we found evidence that GPA-7 and the nuclear receptor NHR-22 can interact in the animal. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:479 / 491
页数:13
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