14-16 This amino-acid sequence predicts that the protein DISC1 may act as a scaffolding protein with multiple binding motifs, facilitating formation of protein complexes. The N -terminus (aa 1-347) contains nuclear

localization signals, whereas the C-terminus (aa 348-854) appears to be important, for microtubule and centrosomal targeting,17-19 although no centrosomal localization has been detected so far for the native protein. Although the precise function of DISC1 in the brain is unknown, a number of DISC1 -interacting partners Inhibitors,research,lifescience,medical have been identified, including fasciculation and elongation protein zeta-1 (FEZ1), nuclear distribution element-like (NUDEL), and lissencephaly 1 (LIS1), which are known to play

a role in neuronal development and functioning. Altered interactions between DISC1 and its binding partners are currently being investigated in order to understand more accurately the biology of DISC1 as a schizophrenia susceptibility gene. DISC1 molecular pathway In an effort Inhibitors,research,lifescience,medical to understand the cellular function of DISC1, yeast-two hybrid studies have been used to identify molecular Inhibitors,research,lifescience,medical interactors of DISC1. It, was found that, DISC1 has numerous binding partners, including NUDEL, FEZ1, activating transcription factor (ATT’) 4/5, and microtubule-associated protein 1 A (MAPI A).15,17,18 NUDEL is a component of a pathway involved in cytoplasmic dynein movement, and is involved in neurofilament assembly, neuronal migration, and development of neurite morphology.20-25 Overexpression of truncated DISC1 protein inhibits neurite outgrowth in PCI 2 cells, suggesting that the DISC1-NUDEL

complex may be involved in neuronal outgrowth.15,25,26 The hypothetical peptide product, resulting from Inhibitors,research,lifescience,medical the Scottish translocation removes the interaction domain for NUDEL. The defective DISC1-NUDEL complex may be a cause of neabnormalities in schizophrenia.19 Recently, it has been shown that NUDEL oligopeptidase activity is under tight, Inhibitors,research,lifescience,medical regulation through binding to DISC1, since a mutation very close to the DISC1-binding site of NUDEL abolishes this activity.27 Interestingly, NUDEL cleaves a number of neuropeptides in vitro, some of which have previously been implicated in the pathophysiology of schizophrenia, including neurotensin (NT).25,29 NT receptor agonists WEEL inhibitor mw may be potential antipsychotics; thus, inhibition of NUDEL could lead to increase in local concentration of NT, which may have an antipsychotic effect.27 Altered subcellular distribution of DISC1 has been reported in patients with psychosis and alcohol/substance abuse, with increased ratios of nuclear to cytoplasmic DISC1 protein levels in patients.30 Cell culture studies in cortical neurons have found Selleckchem WP1130 evidence that DISC1 may colocalize with mitochondrial markers, and that its subcellular targeting is independent of the NUDEL-binding site.