| 1 | Psychiatr. Genet. 2009 Aug 19: 165-70 |
|---|---|
| PMID | 19451863 |
| Title | No evidence for excess runs of homozygosity in bipolar disorder. |
| Abstract | Recent studies have reported large common regions of homozygosity (ROHs) that are the result of autozygosity, that is, the cooccurrence within individuals of long haplotypes that have a high frequency in the population. A recent study reports that such regions are found more commonly in individuals withschizophreniacompared with controls, and identified nine 'risk ROHs' that were individually more common in cases. Of these, four contained or neighboured genes associated withschizophrenia(NOS1AP/UHMK1, ATF2, NSF and PIK3C3). We have applied the same methodology to a UK sample of 506 cases with bipolar disorder and 510 controls. There was no overall excess of common ROHs among bipolar individuals. With one exception, the haplotypes accounting for the ROHs appeared to be distributed according to the Hardy-Weinberg equilibrium. One ROH was individually more common among cases (uncorrected P = 0.0003). This ROH spanned the chromosome 2p23.3 geneITSN2(the gene for intersectin 2 isoform 2). However, inspection of the homozygous haplotypes and haplotype-based tests for association failed to provide a clearer understanding of why this ROH was occurring more commonly. Overall, we conclude that, in contrast withschizophrenia, common ROHs are rarely associated with susceptibility to bipolar disorder. This supports the idea that predominantly different genes are increasing susceptibility toschizophreniaand bipolar affective disorders. |
| SCZ Keywords | schizophrenia |
| 2 | PLoS ONE 2012 -1 7: e36023 |
| PMID | 22558309 |
| Title | Intersectin (ITSN) family of scaffolds function as molecular hubs in protein interaction networks. |
| Abstract | 的成员intersectin (ITSN) family of scaffold proteins consist of multiple modular domains, each with distinct ligand preferences. Although ITSNs were initially implicated in the regulation of endocytosis, subsequent studies have revealed a more complex role for these scaffold proteins in regulation of additional biochemical pathways. In this study, we performed a high throughput yeast two-hybrid screen to identify additional pathways regulated by these scaffolds. Although several known ITSN binding partners were identified, we isolated more than 100 new targets for the two mammalian ITSN proteins, ITSN1 andITSN2. We present the characterization of several of these new targets which implicate ITSNs in the regulation of the Rab and Arf GTPase pathways as well as regulation of the disrupted inschizophrenia1 (DISC1) interactome. In addition, we demonstrate that ITSN proteins form homomeric and heteromeric complexes with each other revealing an added level of complexity in the function of these evolutionarily conserved scaffolds. |
| SCZ Keywords | schizophrenia |