• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1002/ajmg.b.30785
PMID:18484086
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。

相似文献

1
PPP2R2B CAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implications.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
Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):124-9. doi: 10.1002/ajmg.b.30785.
2
Association between CAG repeat length in the PPP2R2B gene and Alzheimer disease in the Japanese population.日本人群 PPP2R2B 基因 CAG 重复长度与阿尔茨海默病的关联。
Neurosci Lett. 2011 Jan 10;487(3):354-7. doi: 10.1016/j.neulet.2010.10.055. Epub 2010 Oct 26.
3
Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12.12型脊髓小脑共济失调的神经病理学与细胞发病机制
Mov Disord. 2015 Nov;30(13):1813-1824. doi: 10.1002/mds.26348. Epub 2015 Sep 4.
4
Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12.在PPP2R2B基因中鉴定出46个CAG重复序列,可能是SCA12最短的致病等位基因。
Parkinsonism Relat Disord. 2015 Apr;21(4):398-401. doi: 10.1016/j.parkreldis.2015.01.006. Epub 2015 Jan 17.
5
Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B.12 型脊髓小脑共济失调的临床行为和 PPP2R2B 中异常的 CAG 重复长度中间型。
Brain. 2017 Jan;140(1):27-36. doi: 10.1093/brain/aww269. Epub 2016 Nov 17.
6
SCA8 repeat expansion: large CTA/CTG repeat alleles in neurological disorders and functional implications.SCA8重复序列扩增:神经疾病中的大CTA/CTG重复等位基因及其功能意义
Hum Genet. 2009 May;125(4):437-44. doi: 10.1007/s00439-009-0641-x. Epub 2009 Feb 20.
7
Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from Taiwan.台湾汉族人群中钙激活钾通道(KCNN3)基因多态性CAG重复序列与精神分裂症的遗传关联研究。
Mol Psychiatry. 1999 May;4(3):271-3. doi: 10.1038/sj.mp.4000482.
8
Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.17型脊髓小脑共济失调中TATA结合蛋白基因中44至47个CAG/CAA重复序列扩增的可能降低的外显率。
Arch Neurol. 2004 Feb;61(2):209-12. doi: 10.1001/archneur.61.2.209.
9
The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expression.SCA12 中的 CAG 重复序列作为顺式元件,上调 PPP2R2B 的表达。
Hum Genet. 2010 Aug;128(2):205-12. doi: 10.1007/s00439-010-0843-2. Epub 2010 Jun 9.
10
SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia.脊髓小脑共济失调12型:一种罕见突变导致一种罕见的脊髓小脑共济失调。
Brain Res Bull. 2001;56(3-4):397-403. doi: 10.1016/s0361-9230(01)00596-2.

引用本文的文献

1
Association between MAPK and PI3K/Akt signaling pathway-related gene polymorphisms and migraine.MAPK 和 PI3K/Akt 信号通路相关基因多态性与偏头痛的关系。
Mol Genet Genomic Med. 2024 Aug;12(8):e2503. doi: 10.1002/mgg3.2503.
2
Tremor-associated short tandem repeat intermediate and pathogenic expansions in familial essential tremor.家族性特发性震颤中与震颤相关的短串联重复序列中间和致病性扩增
Brain Commun. 2024 Jun 29;6(4):fcae217. doi: 10.1093/braincomms/fcae217. eCollection 2024.
3
Early-onset familial essential tremor is associated with nucleotide expansions of spinocerebellar ataxia in China.
早发性家族性特发性震颤与中国脊髓小脑共济失调的核苷酸扩展有关。
Mol Biol Rep. 2024 Jan 16;51(1):113. doi: 10.1007/s11033-023-09023-x.
4
Genetic Risk Factors for Essential Tremor: A Review.特发性震颤的遗传风险因素:综述。
Tremor Other Hyperkinet Mov (N Y). 2020 Jun 11;10:4. doi: 10.5334/tohm.67.
5
PPP2R2B hypermethylation causes acquired apoptosis deficiency in systemic autoimmune diseases.PPP2R2B 甲基化导致系统性自身免疫性疾病获得性细胞凋亡缺陷。
JCI Insight. 2019 Jul 23;5(16):126457. doi: 10.1172/jci.insight.126457.
6
Exploration of CAG triplet repeat in nontranslated region of SCA12 gene.SCA12基因非翻译区CAG三联体重复序列的探索
J Genet. 2016 Jun;95(2):427-32. doi: 10.1007/s12041-016-0624-3.
7
Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12.12型脊髓小脑共济失调的神经病理学与细胞发病机制
Mov Disord. 2015 Nov;30(13):1813-1824. doi: 10.1002/mds.26348. Epub 2015 Sep 4.
8
Identification and functional analysis of variant haplotypes in the 5'-flanking region of protein phosphatase 2A-Bδ gene.鉴定和功能分析蛋白磷酸酶 2A-Bδ 基因 5'侧翼区变异单倍型。
PLoS One. 2012;7(4):e35524. doi: 10.1371/journal.pone.0035524. Epub 2012 Apr 23.
9
Role of the CCAAT-binding protein NFY in SCA17 pathogenesis.CCAAT 结合蛋白 NFY 在 SCA17 发病机制中的作用。
PLoS One. 2012;7(4):e35302. doi: 10.1371/journal.pone.0035302. Epub 2012 Apr 17.
10
Protein phosphatases and Alzheimer's disease.蛋白质磷酸酶与阿尔茨海默病。
Prog Mol Biol Transl Sci. 2012;106:343-79. doi: 10.1016/B978-0-12-396456-4.00012-2.