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糖尿病患者与百岁老人的线粒体细胞色素b基因单核苷酸多态性分析 被引量:1

Analysis of the mitochondrial cytochrome b genes single nucleotide polymorphisms (SNPs) in diabetics and centenarians
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摘要 目的分析2型糖尿病(DM)患者和百岁老人线粒体细胞色素b(Cyt-b)基因的单核苷酸多态性(SNPs)。方法提取96名DM患者和96名百岁老人的外周血单个核细胞中的总DNA,用PCR法扩增、荧光DNA测序,同修订版Cambridge的碱基序列比较检出SNPs。结果两组除共同发现的29处SNPs外,每人相当的SNPs持有数以及两组除共同发现的12处氨基酸置换外,每人相当的SNPs持有数差异均有统计学意义(P=0.01,P=0.02)。从标准氨基酸配列到置换后的氨基酸配列的逸脱值(Grentham值)两组相比差异也有统计学意义(P=0.03)。结论糖尿病组线粒体Cyt-b基因持有多数的SNPs是有害的,从标准氨基酸配列到置换后的氨基酸配列的逸脱值与百岁组相比也呈现高值。 Objective We analyzed SNPss and the deviation from the standard sequence in Cyt-b of mitochondrial DNA in 96 patients with type 2 diabetes and 96 centenarians. Methods Total DNA was extracted from the blood of 96 type 2 diabetes patients and 96 centenarians. Mitochondrial Cyt-b genes were amplified by use o,f oligonucleotide primers. Sequences were analyzed by direct sequencing. Mitochondrial SNPss were identified by comparison with the revised Cambridge reference sequence. Results The number of the carried SNPss with each individual in diabetes group was significantly higher than that in centenarians group when the shared common SNPss were excluded from summation (P=0.01). The number of carried SNPss of each individual in type 2 diabetes group was significantly higher than that in centenarians group when the shared common amino acid replacements were excluded from summation (P=0.02). The deviation from the standard sequence in diabetes group was significantly higher than that in centenarians group (P=0. 03). Conclusions The most mitochondrial SNPss within a species are mildly deleterious in type 2 diabetes. The deviation from the standard sequence in Cyt-b is higher in type 2 diabetes than in centenarians.
出处 《中国糖尿病杂志》 CAS CSCD 北大核心 2008年第5期257-259,共3页 Chinese Journal of Diabetes
关键词 线粒体 细胞色素B 多态性 单核苷酸 糖尿病 2型 百岁老人 Mitochondrial Cytochrome b Polymorphism, single nucleotide Diabetes, type 2Centenarians
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  • 1Tanaka M, Gong J, Zhang J, et al. Mitochondrial genotype associated with longevity and its inhibitory effect on mutagenesis. Meeh Ageing Dev,2000,116 : 65-76.
  • 2Tanaka M, Gong J, Zhang J, et al. Mitochondrial genotype associated with longevity. Lancet, 1998,351 : 185-186.
  • 3Hirose N. Correlates of nutritional status in Japanese centenarians. New York,Spring publishing company, 2000.61-76.
  • 4Tanaka M, Hayakawa M, and Ozawa T. Automated sequencing mitochondrial DNA. Mechods Enzymol, 1996,264 :407-421.
  • 5Anderson S,lankier AT, Barrell BG, et al. Sequence and organization of the human mitochondrial genome. Nature, 1981,290 : 457-465.
  • 6Andrews RM,Kubacka I, Chirmery PF, et al. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet,1999,23:147.
  • 7翁建平.线粒体基因突变糖尿病的现状及筛查与诊治的建议[J].中华医学杂志,2005,85(28):1951-1956. 被引量:45
  • 8Ehm MG, Nelson MR, Spurr NK. Guidelines for conducting and reporting whole genome/large scale association studies. Hun MolGenet, 2005,14 : 2485-2488.
  • 9Carlson CS,Ebrle MA,Kmglyak L, et al. Mappong complex disease loci in whole genome association studies. Nature, 2004,429:4462-4521.

二级参考文献39

  • 1张庆,曾瑞萍,杜传书,修玲玲,程桦.家族性糖尿病中线粒体tRNA^(Leu(UUR))基因突变的发生率及临床特点[J].中山大学学报(医学科学版),1997,17(S1):62-65. 被引量:3
  • 2张秀英,张胜兰,克丙申,姜兆顺,孙荣.线粒体tRNA^(Leu(UUR))A3243G基因突变与2型糖尿病的相关研究[J].中华医学遗传学杂志,2004,21(2):168-170. 被引量:5
  • 3项坤三,王延庆,吴松华,陆惠娟,郑泰山,孙多奇,翁青,贾伟平,沈卫平,浦鎏,何进卫.线粒体tRNA^(Leu(UUR))基因突变糖尿病──患病率估测、临床特点及基因诊断途径[J].中国糖尿病杂志,1995,3(3):129-135. 被引量:34
  • 4Ng MC,Yeung VT,Chow CC, et al. Mitochondrial DNA A3243 Gmutation in patients with early-or late-onset type 2 diabetes mellitus in Hong Kong Chinese. Clin Endocrinol. 2000, 52: 557-564.
  • 5Goto Y, Horai S. A mutation in the tRNA^Leu(UUR) gene associated with MELAS subgroup in mitochondrial encephalomyopathies.Nature, 1990, 348: 651-653.
  • 6Nakagawa Y, Ikegami H, Yamato E, et al. A new mitochondrial DNA mutation associated with non-insulin-dependent diabetes mellitus. Biochem Biophys Res Commun, 1995, 209 : 664-666.
  • 7Odawara M, Sasaki K, Yamashita K, et al. A G-to-A substitution at nucleotide position 3316 in mitochondrial DNA is associated with Japanese non-insulin-dependent diabetes mellitus. Biochem Biophys Res Commun, 1996, 227:147-151.
  • 8Nakano S, Fukuda M, Hotta F, et al. Mitochondrial DNA point mutation at nucleotide pair 3316 in a Japanese family with heterogeneous phenotypes of diabetes. Endo J, 1998, 45: 625-630.
  • 9Ji LN, Hou XM, Han XY. Prevalence and clinical chararcteristics of mitochondrial tRNA^Leu(UUR) mt3243A→G and ND1 gene mt 3316GA mutations in Chinese patients with type 2 diabetes. Nail Med J China(English) ,2001,114 : 1205-1207.
  • 10Hirai M, Suzuki S, Onoda M, et al. Mitochondrial DNA 3394 mutation in the NADH dehydro-genase subunit 1 associated with noninsulin-dependent diabetes mellitus. Biochem Biophys Res Commun,1996, 219: 951-955.

共引文献44

同被引文献28

  • 1李东,周新,李霞,张红梅.糖尿病与线粒体ND1点突变的关系[J].中国老年学杂志,2005,25(6):629-631. 被引量:6
  • 2韩琤波,李凡,毛晓韵,张淑敏,吴东瑛,辛彦.线粒体DNA转录表达与胃癌发生关系的研究[J].中国肿瘤临床,2006,33(21):1205-1209. 被引量:4
  • 3Kang S,Seo S,Hill J,et al.Changes in gene expression in latent HSV-1-infected rabbit trigeminal ganglia following epinephrine iontophoresis[J].Curr Eye Res,2003,26 (3/4):225-229.
  • 4Inoue JG,Miya M,Tsukamoto K,et al.Complete mitochondrial DNA sequence of Conger myriaster (teleostei:Anguilliformes): novel gene order for vertebrate genomes andthe phylogenetic implications for anguilliform families[J].J Mol Evol,2001,52(4): 311-320.
  • 5Zedoni M,Gellera C,Antozzi C,et al.Matemally Inherited Myopathy: association with Mutationin Mirochondrial DNA tRNA[J].Lancet, 1991,338(8760): 143-147.
  • 6Hochhauser D.Relevance of mitochondrial DNA in cancer[J]. Lancet,2000,356(7): 181-182.
  • 7Yaron Y, Orr-Ortreger A.New genetic principles[J].Clin Obstet Gynecol,2002,45(3):593-604.
  • 8Sugie K,Nishino I.Complex IV(cytochrome c oxidase)[J].Nippon Rinsho,2002,60(Suppl 4):490-49.
  • 9Pecina P, Houstkova H,Hansikova H,et al.Genetic defects of cytochrome e oxidase assembly[J].Physiol Res,2004,53(Suppl 1):S213-S223.
  • 10Watanabe Y, Shiozuka K,Ikeda T, et al.Cloning of PCPTP1-Ce encoding protein tyrosine phosphatase from the rat cerebellum and its restricted expression in Purkinje cells[J].Brain Res Mol Brain Res, 1993,58(1/2):69.

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