Journal of Capital Medical University ›› 2011, Vol. 32 ›› Issue (6): 767-770.doi: 10.3969/j.issn.1006-7795.2011.06.012

• 帕金森病的发病机制研究 • Previous Articles     Next Articles

Promoter methylation analysis of seven clock genes in Parkinson's disease

LIN Qing-ling, CAI Yan-ning, DING Hui, GU Zhu-qin, MA Jing-hong, CHEN Biao   

  1. Department of Neurobiology, Xuanwu Hospital, Capital Medical University;Key Laboratory for Neurodegenerative Diseases, Ministry of Education;Beijing Geriatric Medical Research Center, Beijing 100053, China
  • Received:2011-10-16 Revised:1900-01-01 Online:2011-12-21 Published:2011-12-21

Abstract: Objective To investigate the relationship between polymorphism in the pitx3 gene and hereditary susceptibility of late-onset sporadic Parkinson's disease(PD). Methods Three pitx3 single nucleotide polymorphisms(SNPs), including rs2281983, rs4919621 and rs3758549 were examined in 509 late-onset sporadic PD patients and 494 healthy controls. Genotyping was carried out in all subjects using a ligase detection reaction(LDR). Additionally, about 10% of the samples were randomly selected, and retested by direct DNA sequencing. Results Allele and genotype frequencies did not differ between the patients and controls for all three SNPs(rs2281983, rs4919621 and rs3758549). Conclusion Three pitx3 SNPs do not contribute to the risk of developing PD in late-onset sporadic PD in this Chinese population.

Key words: Parkinson's disease, promoter methylation, clock genes

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