Quantitative Proteomic and Genetic Analyses of the Schizophrenia Susceptibility Factor Dysbindin Identify Novel Roles of the Biogenesis of Lysosome-Related Organelles Complex 1

被引:70
作者
Gokhale, Avanti
Larimore, Jennifer
Werner, Erica [2 ]
So, Lomon
Moreno-De-Luca, Andres [3 ,6 ]
Lese-Martin, Christa [3 ]
Lupashin, Vladimir V. [7 ]
Smith, Yoland [4 ,5 ]
Faundez, Victor [1 ]
机构
[1] Emory Univ, Sch Med, Dept Cell Biol, Atlanta, GA 30322 USA
[2] Emory Univ, Dept Biochem, Atlanta, GA 30322 USA
[3] Emory Univ, Dept Human Genet, Atlanta, GA 30322 USA
[4] Emory Univ, Dept Neurol, Atlanta, GA 30322 USA
[5] Emory Univ, Yerkes Natl Primate Res Ctr, Atlanta, GA 30322 USA
[6] Geisinger Hlth Syst, Genom Med Inst, Danville, PA 17822 USA
[7] Univ Arkansas Med Sci, Dept Physiol & Biophys, Little Rock, AR 72205 USA
基金
美国国家卫生研究院;
关键词
HERMANSKY-PUDIAK-SYNDROME; PROTEIN GLYCOSYLATION; MEMBRANE-PROTEINS; BIPOLAR DISORDER; PUDLAK-SYNDROME; CELL BIOLOGY; AMINO-ACIDS; COG COMPLEX; BLOC-1; TRAFFICKING;
D O I
10.1523/JNEUROSCI.5640-11.2012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Biogenesis of Lysosome-Related Organelles Complex 1 (BLOC-1) is a protein complex containing the schizophrenia susceptibility factor dysbindin, which is encoded by the gene DTNBP1. However, mechanisms engaged by dysbindin defining schizophrenia susceptibility pathways have not been quantitatively elucidated. Here, we discovered prevalent and novel cellular roles of the BLOC-1 complex in neuronal cells by performing large-scale Stable Isotopic Labeling of Cells in Culture (SILAC) quantitative proteomics combined with genetic analyses in dysbindin-null mice (Mus musculus) and the genome of schizophrenia patients. We identified 24 proteins that associate with the BLOC-1 complex, many of which were altered in content/distribution in cells or tissues deficient in BLOC-1. New findings include BLOC-1 interactions with the COG complex, a Golgi apparatus tether, and antioxidant enzymes peroxiredoxins 1-2. Importantly, loci encoding eight of the 24 proteins are affected by genomic copy number variation in schizophrenia patients. Thus, our quantitative proteomic studies expand the functional repertoire of the BLOC-1 complex and provide insight into putative molecular pathways of schizophrenia susceptibility.
引用
收藏
页码:3697 / 3711
页数:15
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