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台湾汉族人群中PPP2R2B基因CAG重复序列长度:神经和精神疾病的关联分析及潜在功能意义

PPP2R2B CAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implications.

作者信息

Chen Chiung-Mei, Hou Yi-Ting, Liu Ju-Yun, Wu Yih-Ru, Lin Chih-Hsin, Fung Hon-Chung, Hsu Wen-Chuin, Hsu Yuying, Lee Shen-Hung, Hsieh-Li Hsiu-Mei, Su Ming-Tsan, Chen Shui-Tein, Lane Hsien-Yuan, Lee-Chen Guey-Jen

机构信息

Department of Neurology, Chang Gung Memorial Hospital, Chang-Gung University College of Medicine, Taipei, Taiwan.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):124-9. doi: 10.1002/ajmg.b.30785.

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 of PPP2R2B CAG repeat polymorphism with Taiwanese AD, essential tremor (ET), Parkinson's disease (PD), and schizophrenia and 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%]). The PPP2R2B transcriptional 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 the PPP2R2B gene CAG repeat polymorphism may be functional and may, in part, play a role in conferring susceptibility to AD and ET in Taiwan.

摘要

PPP2R2B是一种在全脑神经元中广泛表达的蛋白质,可调节与微管相关蛋白tau及其他底物的蛋白磷酸酶2A(PP2A)活性。PP2A活性改变与脊髓小脑共济失调12型、阿尔茨海默病(AD)及其他tau蛋白病有关。通过病例对照研究和报告基因检测,我们调查了PPP2R2B CAG重复多态性与台湾地区AD、特发性震颤(ET)、帕金森病(PD)和精神分裂症的关联,并阐明了这种多态性的功能意义。患者和对照之间等位基因的分布无显著差异,10、13和16个三联体长度的等位基因占68.6 - 76.1%。两组均未检测到扩增的等位基因。然而,携带短的5、6和7个三联体等位基因的个体在AD患者(5/180 [2.8%],Fisher精确检验,P = 0.003;包括2例纯合子)和ET患者(4/132 [3.0%],Fisher精确检验,P < 0.001)中的频率显著高于对照组(1/625 [0.2%])。在神经母细胞瘤和胚胎肾细胞中,含有(CAG)(5 - 7)等位基因的荧光素酶报告基因构建体中的PPP2R2B转录活性显著低于含有常见的10、13和16个三联体等位基因的构建体。因此,我们的初步结果表明,PPP2R2B基因CAG重复多态性可能具有功能,且可能在一定程度上在台湾地区AD和ET易感性中发挥作用。

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