Disrupted in schizophrenia 1 interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia

被引:330
作者
Camargo, L. M.
Collura, V.
Rain, J-C
Mizuguchi, K.
Hermjakob, H.
Kerrien, S.
Bonnert, T. P.
Whiting, P. J.
Brandon, N. J.
机构
[1] Merck & Co Inc, Merck Res Labs, Boston, MA 02115 USA
[2] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[3] HYBRIGEN SA, Paris, France
[4] Univ Cambridge, Ctr Math Sci, Cambridge, England
[5] EBI Hinxton, European Bioinformat Inst, Dept Prote Serv Grp, Cambridge, England
[6] Merck Sharp & Dohme Ltd, Neurosci Res Ctr, Dept Mol & Cellular Neurosci, Harlow CM20 2QR, Essex, England
关键词
synapse; schizophrenia; neurodevelopment; dysbindin; DISC1; cognition;
D O I
10.1038/sj.mp.4001880
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
Disrupted in Schizophrenia 1 (DISC1) is a schizophrenia risk gene associated with cognitive deficits in both schizophrenics and the normal ageing population. In this study, we have generated a network of protein-protein interactions ( PPIs) around DISC1. This has been achieved by utilising iterative yeast-two hybrid (Y2H) screens, combined with detailed pathway and functional analysis. This so-called 'DISC1 interactome' contains many novel PPIs and provides a molecular framework to explore the function of DISC1. The network implicates DISC1 in processes of cytoskeletal stability and organisation, intracellular transport and cell-cycle/division. In particular, DISC1 looks to have a PPI profile consistent with that of an essential synaptic protein, which fits well with the underlying molecular pathology observed at the synaptic level and the cognitive deficits seen behaviourally in schizophrenics. Utilising a similar approach with dysbindin (DTNBP1), a second schizophrenia risk gene, we show that dysbindin and DISC1 share common PPIs suggesting they may affect common biological processes and that the function of schizophrenia risk genes may converge.
引用
收藏
页码:74 / 86
页数:13
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