期刊文献+

广西巴马长寿人群对氧磷酯酶-1基因多态性分析 被引量:2

Genetic polymorphisms of PON1 in longevous people in Bama county of Guangxi province
下载PDF
导出
摘要 目的探讨PON1基因Q192R位点在广西巴马地区不同人群中的频率及PON1基因多态性与巴马地区长寿现象的相关性。方法采用TaqMan探针实时荧光PCR技术对广西巴马长寿地区123例长寿老人(年龄90岁以上,长寿组)以及巴马长寿地区138例无长寿史的健康成年人(年龄24~87岁,对照1组)、巴马非长寿地区147例无长寿史的健康成年人(年龄48~89岁,对照2组)和南丹地区144例无长寿史的健康成年人(年龄21~83岁,对照3组)的PON1基因进行基因分型。结果长寿组与各对照组比较,等位基因和基因型分布差异存在统计学意义(P<0.05)。结论该多态性位点与地域有关,与巴马长寿地区的长寿现象是否有关还需进一步验证。 Objective To investigate the correlation between Q192R single nucleotide polymorphisms(SNP) of PON1 gene and hu- man longevity in Bama county. Methods Genotyping of PON1 gene was performed by TaqMan-PCR technique for 123 longevous people (aged 90 - 110, longevity group) from Bama longevity area, 138 healthy cases without long life history from the same area (aged 24 - 87, control group 1 ), 147 healthy cases without long life history from Bama non-longevity area (aged 48 - 89 ,control group 2) and 143 healthy controls without long life history from Nandan (aged 21-83, control group 3). Results There were statistically significant change of some frequencies of alleles and genotypes between longevity group and control group 3 ( P 〈 O. 05). Conclusions These data suggest a modest as- sociation between the PON1 gene Q192R and district. It needs a further research to confirm whether there have any relationship between PON1 gene Q192R and longevity phenomenon in Bama longevity area.
出处 《中国老年学杂志》 CAS CSCD 北大核心 2012年第7期1338-1340,共3页 Chinese Journal of Gerontology
基金 国家自然科学基金资助项目(No.30560166 No.81060246) 广西科学基金资助项目(桂科自0991115桂科青0832032) 广西科学研究与技术开发项目(桂科能0815011-6-5)
关键词 长寿 对氧磷酯酶-1 等位基因 多态性 Longevity Paraoxonase-1 Allele Polymorphisms
  • 相关文献

参考文献4

二级参考文献27

共引文献27

同被引文献20

  • 1玛依拉.吾甫尔,周文郁,顾明亮,方鸣武,程祖亨,邱长春.新疆维吾尔族人自然长寿与HLADRB、ACE基因的关联分析[J].基础医学与临床,2005,25(6):492-497. 被引量:10
  • 2刘辉.长寿研究中长寿人群和对照组的确定[J].中国老年学杂志,2007,27(7):678-679. 被引量:14
  • 3Olmos Y,Sanchez-Gomez FJ,Wild B,et al. SirT1 regulation of antioxidant genes is dependent on the formation of a FoxO3a/PGC- 1 alpha complex [ J]. Antioxid Redox Signal 2013,19 : 1507-1521.
  • 4Tran H, Brunet A, Grenier JM, et al. DNA repair pathway stimulated by the forkhead transcription factor FOXO3A through the Gadd45 protein[ J]. Science, 2002,296: 530-534.
  • 5Notas G,Alexaki VI,Kampa M,et al. APRIL binding to BCMA activates a JNK2-FOXO3-GADD45 pathway and induces a GJM cell growth arrest in liver cells [J]. J Immunol,2012,189:4748- 4758.
  • 6Vrailas-Mortimer AI,del Rivero T,Mukherjee S,et al. A muscle- specific p38 MAPK/Mef2/MnSOD pathway regulates stress,motor function, and life span in Drosophila [ J ]. Dev Cell, 2011,10,21 : 783-795.
  • 7Tomoko M,Atef NH,Adrian BS,et al. GADD45 regulates GJM arrest,DNA aepair,and cell death in keratinocytes following ultraviolet exposure[ J ]. J Invest Dermatol, 2002,119 : 22-26.
  • 8Gupta SK,Gupta M,Hoffman B,et al. Hematopoietic cells from Gadd45a-deficient and Gadd45b-deficient mice exhibit impaired stress responses to acute stimulation with cytokines, myeloablation and inflammation[ J ]. Oncogene, 2006,25 : 5537-5546.
  • 9Hinault MP,Ben-Zvi A,Goloubinoff P.Chaperones and proteases:cellular fold-controlling factors of proteins in neurodegenerative diseases and aging[J].J Mol Neurosci,2006;30(3):249-65.
  • 10Lindenstrom E,Bogsen G,Nyboe J,et al.Influence of total cholesterol,high density lipoprotein cholesterol,and triglycerides on risk of cerebrovascular disease:the Copenhagen City Heart Study[J].BMJ,1994;309(6946):11-5.

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部