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一种新发现的线粒体DNA大片段缺失与衰老的关系初探 被引量:3

Preliminary study of a new deletion of mitochondria DNA fragment in human peripheral blood cells and its relation to the aging
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摘要 目的 在人外周血细胞中筛选新的线粒体DNA(mtDNA)大片段缺失突变 ,探讨mtDNA大片段缺失突变与衰老的关系。 方法 以人外周血细胞DNA为模板 ,进行聚合酶链反应 (PCR)扩增 ,产物克隆、测序。用PCR半定量方法测定 <6 0岁组和≥ 6 0岁组中突变型与野生型的比例。 结果 在人外周血细胞中发现 1条长达 13 1kb的mtDNA缺失突变 ,<6 0岁组和≥ 6 0岁组突变型与野生型的比例 ,差异有显著性。 结论 该突变以前未见报道 ,可能是一种与衰老有关的缺失突变。 Objective To screen a new deletion in mitochondria(mtDNA) fragment in human peripheral blood cells, and study the relationship between the mtDNA deletion and the aging. Methods DNA extracted from human peripheral blood cells was used as PCR templates. The PCR products were cloned and sequenced. Semi quantitative PCR was also used in detecting the ratio of deleted mtDNA to wild type mtDNA. Results There was a 13 1 kb mtDNA deleted in human peripheral blood cells, and the deletion ratio between <60 age group and ≥60 age group was significantly different. Conclusions To our knowledge,this deletion has not been reported before and was the longest deleted fragment in human mitochondrial genome and it might be an aging related deletion mutation.
出处 《中华老年医学杂志》 CAS CSCD 北大核心 2001年第2期120-123,共4页 Chinese Journal of Geriatrics
关键词 线粒体DNA 基因缺失 衰老 疾病 基因突变 DNA Mitochondrial Gene deletion Aging
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  • 1徐叔云,药理实验方法学(第2版),1991年,948页
  • 2毛泽斌,北京医科大学学报,1997年,29卷,27页
  • 3童坦君,医学老年学.衰老与长寿,1995年,142页
  • 4王文,动物学报,1993年,14卷,197页

共引文献14

同被引文献40

  • 1周彤,金锡鹏.职业与衰老[J].中华劳动卫生职业病杂志,1996,14(3):170-172. 被引量:14
  • 2[1]Vaziri H,Benchimol S.Reconsititution of telomerase activity in nomal human cells leads to elongation of telomeres and extended replicative life span[J].Curr Biol,1998,8 (5):279-282.
  • 3[2]Yang L,Suwa T,Wright WE,et al.Telomere shortening and decline in replicative potential as a fuction of donor age in human adrenocortical cells[J].Mech Ageing Dev,2001,122(15):1685-1694.
  • 4[3]Tsuji A,Ishiko A,Takasaki T,et al.Estimating age of humans based on telomere shortening[J].Forensic Sci Int,2002,126(3):197-199.
  • 5[4]Kammori M,Nakamura K,Kawahara M,et al.Telomere shortening with aging in human thyroid and parathyroid tissue[J].Exp Gerontol,2002,37(4):513-521.
  • 6[5]Wilson VL,Smith RA,Ma S,et al.Genomic 5-methyldeoxycytidine decreases with age[J].J Biol Chem,1987,262(21):9948-9951.
  • 7[6]Tra J,Kondo T,Lu Q,et al.Infrequent occurrence of age-dependent changes in CpG island methylation as detected by restriction landmark genome scanning[J].Mech Ageing Dev,2002,123(11):1487-1503.
  • 8[7]Harman,D.The biologic clock:the mitochondria?[J].J Am Geriatr Soc,1972,20(4):145-147.
  • 9[8]Hayakawa M,Hattori K,Sugiyama S,et al.Age-associated oxygen damage and mutations in mitochondrial DNA in human hearts[J].Biochem Biophys Res Commun,1992,189(2):979-985.
  • 10[9]Lai LP,Tsai CC,Su MJ,et al.Atrial fibrillation is associated with accumulation of aging-related common type mitochondrial DNA deletion mutation in human atrial tissue[J].Chest,2003,123(2):539-544.

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