| 1 | Am. J. Med. Genet. B Neuropsychiatr. Genet. 2003 Jan 116B: 45-50 |
|---|---|
| PMID | 12497613 |
| Title | CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia. |
| Abstract | The purpose of this study was to determine whether genetic linkage or association could be observed betweenschizophrenia(SZ) and the CAG repeat polymorphisms within the genes KCNN3 (known previously as hSKCa3) andPPP2R2B(linked to Spino-Cerebellar Atrophy 12) in the Xhosa population in South Africa. Neither locus has been studied previously in African populations. The polymorphisms were genotyped in 589 individuals to form samples for Transmission Disequilibrium Test (TDT) analysis (176 unrelated probands, 145 with both parents and 30 with one parent genotyped), linkage analysis (49 families with 54 independent affected sib pairs [ASPs]), and case-control analyses (67 familial cases with a first-degree SZ relative, 101 sporadic cases with no affected first- or second-degree relative, and 90 control cases). No significant differences were found among familial cases, sporadic cases and controls in allele sizes (Kruskal-Wallis tests) or the numbers of alleles with sizes above and below the mean size for each polymorphism. Allele size was not correlated with age of onset (Spearman correlation). No significant evidence for association was observed using TDT analyses for all triads and separately for the familial triads. No significant evidence for linkage was observed for either locus with affected sib pair analysis using the possible triangle method or with Non-Parametric Linkage (NPL) analysis of the multiplex families. In conclusion, no significant evidence for linkage or association with SZ was observed for either polymorphism in this population. |
| SCZ Keywords | schizophrenia, schizophrenic |
| 2 | Schizophr. Res. 2005 Oct 78: 131-6 |
| PMID | 16054804 |
| Title | Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophrenia. |
| Abstract | schizophreniahas a complex and non-Mendelian mode of inheritance. Recently, trinucleotide repeat (TNR)-containing genes have been considered as the candidate genes predisposing toschizophrenia. The purpose of this study was to determine whether a genetic association could be observed betweenschizophreniaand the TNR polymorphisms within the KLHL1AS/SCA8,PPP2R2B/SCA12, and TBP/SCA17 genes. We studied 100 unrelatedschizophreniapatients and 124 controls without evident neurodegenerative or psychiatric disorders. The overall allele frequency distributions of the KLHL1AS/SCA8 andPPP2R2B/SCA12 genes were not significantly different between theschizophrenicpatients and the control subjects (P>0.05). The allele frequency distribution in theschizophrenicpatients was significantly different from that in the controls at the TBP/SCA17 gene (P=0.0149), with an increased frequency of 36 repeats in the patients and two patients carrying 45 TNR expansions were identified. TBP/SCA17 is the TATA box binding protein gene mapped to chromosome 6q27. The study suggests that TNR expansions of the TBP/SCA17 gene may contribute to the genetic risk ofschizophreniain rare cases. |
| SCZ Keywords | schizophrenia, schizophrenic |
| 3 | Schizophr. Res. 2005 Oct 78: 131-6 |
| PMID | 16054804 |
| Title | Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophrenia. |
| Abstract | schizophreniahas a complex and non-Mendelian mode of inheritance. Recently, trinucleotide repeat (TNR)-containing genes have been considered as the candidate genes predisposing toschizophrenia. The purpose of this study was to determine whether a genetic association could be observed betweenschizophreniaand the TNR polymorphisms within the KLHL1AS/SCA8,PPP2R2B/SCA12, and TBP/SCA17 genes. We studied 100 unrelatedschizophreniapatients and 124 controls without evident neurodegenerative or psychiatric disorders. The overall allele frequency distributions of the KLHL1AS/SCA8 andPPP2R2B/SCA12 genes were not significantly different between theschizophrenicpatients and the control subjects (P>0.05). The allele frequency distribution in theschizophrenicpatients was significantly different from that in the controls at the TBP/SCA17 gene (P=0.0149), with an increased frequency of 36 repeats in the patients and two patients carrying 45 TNR expansions were identified. TBP/SCA17 is the TATA box binding protein gene mapped to chromosome 6q27. The study suggests that TNR expansions of the TBP/SCA17 gene may contribute to the genetic risk ofschizophreniain rare cases. |
| SCZ Keywords | schizophrenia, schizophrenic |
| 4 | Am. J. Med. Genet. B Neuropsychiatr. Genet. 2009 Jan 150B: 124-9 |
| PMID | 18484086 |
| Title | PPP2R2B CAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implications. |
| Abstract | PPP2R2B, a protein widely expressed in neurons throughout the brain, regulates the protein phosphatase 2A (PP2A) activity for the microtubule-associated protein tau and other substrates. Altered PP2A activity has been implicated in spinocerebellar ataxia 12, Alzheimer's disease (AD), and other tauopathies. Through a case-control study and a reporter assay, we investigated the association ofPPP2R2BCAG repeat polymorphism with Taiwanese AD, essential tremor (ET), Parkinson's disease (PD), andschizophreniaand clarified the functional implication of this polymorphism. The distribution of the alleles was not significantly different between patients and controls, with 68.6-76.1% alleles at lengths of 10, 13, and 16 triplets. No expanded alleles were detected in either group. However, the frequency of the individuals carrying the short 5-, 6-, and 7-triplet alleles was notably higher in patients with AD (5/180 [2.8%], Fisher's exact test, P = 0.003; including 2 homozygotes) and ET (4/132 [3.0%], Fisher's exact test, P < 0.001) than in the controls (1/625 [0.2%]). ThePPP2R2Btranscriptional activity was significantly lower in the luciferase reporter constructs containing the (CAG)(5-7) allele than in those containing the common 10-, 13-, and 16-triplet alleles in both neuroblastoma and embryonic kidney cells. Therefore, our preliminary results suggest that thePPP2R2B基因CAG重复多态性可能是有趣的ctional and may, in part, play a role in conferring susceptibility to AD and ET in Taiwan. |
| SCZ Keywords | schizophrenia, schizophrenic |