Identification and characterization of Gemin7, a novel component of the survival of motor neuron complex

被引:89
作者
Baccon, J
Pellizzoni, L
Rappsilber, J
Mann, M
Dreyfuss, G [1 ]
机构
[1] Univ Penn, Howard Hughes Med Inst, Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Biochem & Biophys, Sch Med, Philadelphia, PA 19104 USA
[3] Univ So Denmark, Prot Interact Lab, Ctr Expt Bioinformat, DK-5230 Odense, Denmark
[4] Univ So Denmark, Dept Biochem & Mol Biol, DK-5230 Odense M, Denmark
关键词
D O I
10.1074/jbc.M203478200
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
The survival of motor neurons (SMN) protein is the product of the gene mutated or deleted in the neurodegenerative disease, spinal muscular atrophy. SMN is part of a large macromolecular complex that also contains Gemin2, Gemin3, Gemin4, Gemin5, and Gemin6. The SMN complex functions in the assembly of spliceosomal small nuclear ribonucleoproteins and probably other ribonucleoprotein particles. We have identified a novel protein component of the SMN complex termed Gemin7 using native purified SMN complexes and peptide sequencing by mass spectrometry. Coimmunoprecipitation and immunolocalization experiments demonstrate that Gemin7 is a component of the SMN complex and colocalizes with SMN in the cytoplasm and in gems. Binding experiments show that Gemin7 interacts directly with SMN and Gemin6 and mediates the association of Gemin6 with the SMN complex. The amino acid sequence of Gemin7 does not contain any recognizable motifs with the exception of several arginine and glycine repeats that are necessary for its interaction with SMN. Moreover, Gemin7 interacts with several Sm proteins of spliceosomal small nuclear ribonucleoproteins, in particular, with SmE. With the identification of Gemin7, the inventory of the core components of the SMN complex appears essentially complete.
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页码:31957 / 31962
页数:6
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