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线粒体tRNA突变与高血压关系的研究进展 被引量:2

Relationshipof mitochondrial tRNA mutationwith development of hypertension:aresearchprogress
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摘要 线粒体基因突变与多种疾病的发生有关,虽然转移RNA(tRNA)基因只占整个线粒体基因组的10%,但它们却是研究线粒体基因突变与疾病发生关系的热点。既往高血压遗传学的研究主要集中在核基因方面,近年来研究发现线粒体DNA突变可能参与原发性高血压(EH)的发生与发展,且越来越多的线粒体tRNA也被报道与EH的发生和发展密切相关。本文对线粒体tRNA突变与高血压发病的关系及其机制进行了综述。 Mitochondrial DNA mutation is associated with a variety of diseases. Althoughonly constituting 10% of the entire mitochondrial genome,the transfer RNA(tRNA) geneshave become a hotspotin the study concerning the relationship of the mitochondrial gene mutation with diseases. Previous studies on the genetics of hypertension mainlyconcentrated in the nuclear genes, butrecent studies found that mitochondrial DNA mutations may be involved in the occurrence and development of essential hypertension (EH).What’s more, much evidence indicated that close association was found between mitochondrial tRNA with theEH occurrence and development.In this article, we summarized the relationship between themitochondrial tRNA mutation and pathogenesis of hypertension, andreviewed the underlyingmechanism.
出处 《中华老年多器官疾病杂志》 2015年第6期477-480,共4页 Chinese Journal of Multiple Organ Diseases in the Elderly
基金 中国博士后基金(20080431356) 国家自然科学基金项目(81170249,30700305) 北京市科技新星计划(2008A064)
关键词 线粒体 TRNA 原发性高血压 基因突变 mitochondria tRNA essential hypertension gene mutation
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参考文献24

  • 1Levinger L,M-rl M,Florentz C.Mitochondrial tRNA 3'end metabolism and human disease[J].Nucleic Acids Res,2004,32 (18):5430-5441.
  • 2Larsson NG,Clayton DA.Molecular genetic aspects ofhuman mitochondrial disorders[J].Annu Rev Genet,1995,29:151-178.
  • 3DiMauro S,Schon EA.Nuclear power and mitochondrialdisease[J].Nat Genet,1998,19(3):214-215.
  • 4Chinnery PF,Turnbull DM.Mitochondrial DNAmutations in the pathogenesis of human disease[J].MolMed Today,2000,6(11):425-432.
  • 5Maassen JA.Mitochondrial diabetes:pathophysiology,clinical presentation,and genetic analysis[J].Am J MedGenet,2002,115(1):66-70.
  • 6Yasukawa T,Hino N,Suzuki T,et al.A pathogenic pointmutation reduces stability of mitochondrial mutanttRNA(Ile)[J].Nucleic Acids Res,2000,28(19):3779-3784.
  • 7Hajjar I,Kotchen JM,Kotchen TA.Hypertension:trendsin prevalence,incidence,and control[J].Annu Rev PublicHealth,2006,27:465-490.
  • 8Fuentes RM,Notkola IL,Shemeikka S,et al.Familialaggregation of blood pressure:a population-based familystudy in eastern Finland[J].J Hum Hypertens,2000,14(7):441-445.
  • 9Yang Q,Kim SK,Sun F,et al.Maternal influence onblood pressure suggests involvement of mitochondrialDNA in the pathogenesis of hypertension:theFramingham Heart Study[J].J Hypertens,2007,25(10):2067-2073.
  • 10Wilson FH,Hariri A,Farhi A,et al.A cluster of metabolicdefects caused by mutation in a mitochondrial tRNA[J].Science,2004,306(5699):1190-1194.

二级参考文献47

  • 1Delles C. Mitochondria, maternal transmission and hypertension[J]. J Hypertens, 2007, 25(10): 2001-2003.
  • 2Yang Q, Kim SK, Sun F, et al. Maternal influence on blood pressure suggests involvement of mitochondrial DNA in the pathogenesis of hypertension: the Framingham Heart Study[J]. J Hypertens, 2007, 25(10): 2067-2073.
  • 3Dominiczak AF, Negrin DC, Clark JS, et al. Genes and hypertension: from gene mapping in experimental models to vascular gene transfer strategies[J]. Hypertension, 2000, 35 (1 Pt 2): 164-172.
  • 4Gharavi AG, Phillips RA, Finegood DT, et al. Glycogen synthase polymorphism, insulin resistance and hypertension[J]. Blood Pressure, 1996, 5(2): 86-90.
  • 5Yang W, Huang J, Ge D, et al. Lipoprotein lipase gene is in linkage with blood pressure phenotypes in Chinese pedigrees[J]. Human Genetics, 2004, 115(1): 8-12.
  • 6Motone M, Katsuya T, Ishikawa K, et al. Association between hepatocyte growth factor gene polymorphism and essential hypertension[J]. Hypertens Res, 2004, 27(4): 247- 251.
  • 7Zhao W, Wang L, Lu X, et al. A coding polymorphism of the kallikrein 1 gene is associated with essential hypertension a tagging SNP-based association study in a Chinese Han population[J]. J Hypertens, 2007, 25(9): 1821-1827.
  • 8Geller DS. A mineralocorticoid receptor mutation causing human hypertension[J]. Curr Opin Nephrol Hypertens, 2001, 10(5): 661-665.
  • 9Devereux RB, Alonso DR, Lutas EM, et al. Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings[J]. Am J Cardiol, 1986, 57(6): 450-458.
  • 10Zongbin Li, Yuqi Liu, Li Yang, et al. Maternally inherited hypertension is associated with the mitochondrial tRNA^Ile A4295G mutation in a Chinese family[J]. Biochem Biophys Res Commun, 2008, 367(4): 906-911.

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