Literature DB >> 18484086

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

Chiung-Mei Chen1, Yi-Ting Hou, Ju-Yun Liu, Yih-Ru Wu, Chih-Hsin Lin, Hon-Chung Fung, Wen-Chuin Hsu, Yuying Hsu, Shen-Hung Lee, Hsiu-Mei Hsieh-Li, Ming-Tsan Su, Shui-Tein Chen, Hsien-Yuan Lane, Guey-Jen Lee-Chen.   

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. 2008 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 18484086     DOI: 10.1002/ajmg.b.30785

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  9 in total

1.  The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expression.

Authors:  Chih-Hsin Lin; Chiung-Mei Chen; Yi-Ting Hou; Yih-Ru Wu; Hsiu-Mei Hsieh-Li; Ming-Tsan Su; Guey-Jen Lee-Chen
Journal:  Hum Genet       Date:  2010-06-09       Impact factor: 4.132

2.  Exploration of CAG triplet repeat in nontranslated region of SCA12 gene.

Authors:  Waseem Gul Lone; Imran Ali Khan; Subhadra Poornima; Noor Ahmad Shaik; Angmuthu Kanikannan Meena; Kaipa Prabhakar Rao; Qurratulain Hasan
Journal:  J Genet       Date:  2016-06       Impact factor: 1.166

Review 3.  Protein phosphatases and Alzheimer's disease.

Authors:  Steven P Braithwaite; Jeffry B Stock; Paul J Lombroso; Angus C Nairn
Journal:  Prog Mol Biol Transl Sci       Date:  2012       Impact factor: 3.622

4.  PPP2R2B hypermethylation causes acquired apoptosis deficiency in systemic autoimmune diseases.

Authors:  Iris K Madera-Salcedo; Beatriz E Sánchez-Hernández; Yevgeniya Svyryd; Marcela Esquivel-Velázquez; Noé Rodríguez-Rodríguez; María Isabel Trejo-Zambrano; H Benjamín García-González; Gabriela Hernández-Molina; Osvaldo M Mutchinick; Jorge Alcocer-Varela; Florencia Rosetti; José C Crispín
Journal:  JCI Insight       Date:  2019-07-23

5.  Mitochondrial dysfunction and oxidative stress contribute to the pathogenesis of spinocerebellar ataxia type 12 (SCA12).

Authors:  Yu-Chun Wang; Chi-Mei Lee; Li-Ching Lee; Li-Chu Tung; Hsiu-Mei Hsieh-Li; Guey-Jen Lee-Chen; Ming-Tsan Su
Journal:  J Biol Chem       Date:  2011-04-06       Impact factor: 5.157

6.  Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12.

Authors:  Elizabeth E O'Hearn; Hyon S Hwang; Susan E Holmes; Dobrila D Rudnicki; Daniel W Chung; Ana I Seixas; Rachael L Cohen; Christopher A Ross; John Q Trojanowski; Olga Pletnikova; Juan C Troncoso; Russell L Margolis
Journal:  Mov Disord       Date:  2015-09-04       Impact factor: 10.338

7.  Role of the CCAAT-binding protein NFY in SCA17 pathogenesis.

Authors:  Li-Ching Lee; Chiung-Mei Chen; Hao-Chun Wang; Hsiao-Han Hsieh; I-Sheng Chiu; Ming-Tsan Su; Hsiu-Mei Hsieh-Li; Chung-Hsin Wu; Guan-Chiun Lee; Guey-Jen Lee-Chen; Jung-Yaw Lin
Journal:  PLoS One       Date:  2012-04-17       Impact factor: 3.240

8.  Identification and functional analysis of variant haplotypes in the 5'-flanking region of protein phosphatase 2A-Bδ gene.

Authors:  Hui-Feng Chen; Li-Na Lin; Yu-Xi Chen; Jian-Xin Wan; Jie Luo; Chen-Zi Zhang; Xiao-Jie Li; Yao-Ming Hu; Jian-Rong Mai; Wen Chen; Zhong-Ning Lin; Yu-Chun Lin
Journal:  PLoS One       Date:  2012-04-23       Impact factor: 3.240

Review 9.  Genetic Risk Factors for Essential Tremor: A Review.

Authors:  Vasileios Siokas; Athina-Maria Aloizou; Zisis Tsouris; Ioannis Liampas; Paraskevi Aslanidou; Metaxia Dastamani; Alexandros G Brotis; Dimitrios P Bogdanos; Georgios M Hadjigeorgiou; Efthimios Dardiotis
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2020-06-11
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.