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脂蛋白脂肪酶内含子3C→T突变 被引量:3

A Splice Site Mutation in Intron 3 of the Lipoprotein Lipase Gene Resulting in Hypertriglyceridemia
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摘要 为筛查中国人群脂蛋白脂肪酶基因的突变情况 ,并探讨这些突变对脂蛋白代谢可能产生的影响 ,研究者利用聚合酶链反应—单链构象多态性分析技术 ,对 14 0例人群 (高甘油三酯血症组 5 1例 ,正常对照组 89例 )的脂蛋白脂肪酶基因进行了突变筛查 ,对可疑突变的扩增样品进行DNA序列测定。结果在外显子 4扩增片段 (包括内含子—外显子交界区 )有 2例可疑突变被检出 ,经测序证实均为内含子 3受位剪接位点上游 6bp的C→T转换突变杂合子。由于该突变仅见于重度高甘油三酯血症患者 ,结合国内外相关文献 ,研究者认为我国人群存在脂蛋白脂肪酶基因内含子 3受位剪接位点的C→T突变 ,该突变可能是我国人群高甘油三酯血症的遗传易患因子。 Aim To screen the lipoprotein lipase gene for mutations in Chinese population and to study the possible effects of the mutations on the lipoprotein metabolism. Methods The lipoprotein lipase gene was examined by polymerase chain reaction-single strand conformation polymorphism analysis, and the polymerase chain reaction products showing abnormal pattern on single strand conformation polymorphism were sequenced using dideoxy-mediated chain-termination method. Results Two mutations were found in 140 Chinese people and both were heterozygous C→T transitions at 6 bp upstream from acceptor splicing site of intron 3. Conclusion The mutation in intron 3 of the lipoprotein lipase gene may be the genetic risk of hyperglyceridemia in Chinese population.
出处 《中国动脉硬化杂志》 CAS CSCD 2003年第6期570-572,共3页 Chinese Journal of Arteriosclerosis
基金 天津市自然科学基金 ( 0 3 3 60 73 11)资助
关键词 脂蛋白脂肪酶 聚合酶链反应-单链构象多态性分析 高甘油三酯血症 内含子突变 Lipoprotein Lipase Hyperglyceridemia Intron Mutation Polymerase Chain Reaction Single Strand Conformation Polymorphism
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参考文献10

  • 1[1]Merkel M, Eckel RH, Goldberg IJ. Lipoprotein lipase: genetics, lipid uptake and regulation. J Lipid Res, 2002, 43 (12): 1 997-2 006
  • 2穆云翔.脂蛋白脂肪酶基因突变研究进展[J].中国动脉硬化杂志,2002,10(4):358-362. 被引量:12
  • 3刘欣,曹海燕,陈涛,钟媛,解用虹.121例新生儿载脂蛋白E基因型的分布[J].中国动脉硬化杂志,2001,9(4):337-339. 被引量:4
  • 4[4]Oka K, Tkalcevic GT, Nakano T, Tucker H, Ishimura-Oka K, Brown WV. Structure and polymorphic map of human lipoprotein lipase gene. Biochimi Biophys Acta, 1990, 1 049 (1): 21-26
  • 5[5]Ikeda Y, Takagi A, Nakata Y, Sera Y, Hyoudou S, Hamamoto K, et al. Novel compound heterozygous mutations for lipoprotein lipase deficiency: A G-to-T transversion at the first position of exon 5 causing G154V missense mutation and a 5' splice site mutation of intron 8. J Lipid Res, 2001, 42 (7): 1 072-081
  • 6[6]Ikeda Y, Takagi A, Nakata Y, Sera Y, Hyoudou S, Hamamoto K, et al. A family-based study of hyperinsulinemia and hypertriglyceridemia in heterozygous lipoprotein lipase deficiency. Clin Chim Acta, 2002, 316 (1): 179-185
  • 7[7]Holzl B, Kraft HG, Wiebusch H, Sandhofer A, Patsch J, Sandhofer F, et al. Two novel mutations in the lipoprotein lipase gene in a family with marked hypertriglyceridemia in heterozygous carriers. Potential interaction with the polymorphic marker D1S104 on chromosome 1q21-q23. J Lipid Res, 2000, 41 (5): 734-741
  • 8[8]Rodwell VW. Catabolism of the carbon skeletons of amio acids. In: Murray RK, Granner DK, Mayes PA, Rodwell VW eds. Harper's Biochemistry. 25th ed. Stamford:Appleton & Lange, 2000; 323-346
  • 9[9]Nakamura T, Suehiro T, Yasuoka N, Yamamoto M, Ito H, Yamano T, et al. A novel nonsense mutation in exon 1 and a transition in intron 3 of the lipoprotein lipase gene. J Atheroscler Thromb, 1996, 3 (1): 17-24
  • 10[10]Li J, Kobori K, Kondo A, Yonekawa O, Kanno T. The application of end user computing (EUC) for detection of lipoprotein lipase gene abnormality. Rinsho Byori, 1999, 47 (8): 737-743

二级参考文献9

共引文献14

同被引文献35

  • 1赵郁,穆云翔,杨宇虹,刘新宇,葛林,解用虹.脂蛋白脂肪酶基因突变的研究[J].天津医药,2004,32(11):657-660. 被引量:8
  • 2汪军梅,赵莉莉,孙静,刘新宇,赵郁,解用虹.血脂正常人群检出LPL内含子3C→T突变[J].天津医科大学学报,2005,11(2):159-161. 被引量:2
  • 3Merkel M,Eckel RH,Goldbrg IJ.Lipoprotein lipase:genetics,lipid uptake,and regulation.Lipid Res,2002,43 (12):1 997-006
  • 4Hata A,Robertson M,Emi M.Direct detection and automated sequencing of individual alleles after electrophoretic strand separation:identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene.Nucleic Acids Res,1990,18 (18):5 407-411
  • 5Wei Chen,Sathanur R,Srinivasan,Elkasabanu A,Ellsworth DL,Boerwinkle E.Influence of lipoprotein lipase serine447stop polymorphism on tracking of triglycerides and HDL cholesterol from childhood to adulthood and familial risk of coronary artery disease:the Bogalusa Heart Study.Atherosclerosis,2001,159:367-373
  • 6Clee SM,Loubser O,Cllins J,Kastelein JJP,Hayden MR.The LPL S447X cSNP is assosiated with decreased blood pressure and plasma triglycerides,and reduced risk of coronary artery disease.Clin Genet,2001,60:293-300
  • 7Oliavi U,Christope G,Louis P,Bergeron J,Despres J,Rao D,et al.Genetic variation at the lipoprotein lipase locus and plasma lipoprotein and insulin levels in the Quebec Family Study.Atherosclelerosis,2001,158:199-206
  • 8Kobayashi J,Nishida T,Ameis D,Stahnke G,Schotz MC,Hashimoto H,et al.A heterozygous mutation (the codon for Ser447-a stop codon) in lipoprotein lipase contributes to a defect in lipid interface recognition in a case with type I hyperlipidemia.Biochem Biophys Res Commun,1992,182 (1):70-77
  • 9Takeyoshi M,Miyashita Y,YoshiakiItoh,Satoko T,Yamamori Syunji,Watanabe H,et al.Incidence of lipoprotein lipase genotype for premature termination codon (Ser447-Ter) in Japanese and association with dyslipoproteinemia.Clinica Chimica,1998,275:205-213
  • 10Lee J,Tan CS,Chia KS,Tan CE,Chew SK,Ordovas JM,et al.The lipoprotein lipase S447X polymorphism and plasma lipids:interactions with APOE polymorphisms,smoking,and alcohol consumption.J Lipid Res,2002,45:1 132-139

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