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高血压患者及大鼠线粒体ATPase 6基因的克隆、表达与突变研究
引用本文:周林,万大方,张国元,李宏年,张萍萍,赵新泰,顾健人,Liew C C. 高血压患者及大鼠线粒体ATPase 6基因的克隆、表达与突变研究[J]. 第三军医大学学报, 1999, 21(10): 729-733
作者姓名:周林  万大方  张国元  李宏年  张萍萍  赵新泰  顾健人  Liew C C
作者单位:1. 第三军医大学附属大坪医院野战外科研究所第四研究室,重庆,400042
2. 上海市肿瘤研究所癌基因及相关基因国家重点实验室,上海,200032
3. 第二军医大学长征医院心血管内科,上海,200003
4. (Laboratory for molecular cardiology,University of Toronto, Ontario,M5G 1L5,Canada
摘    要:目的:研究正常血压与高血压鼠以及正常血压与高血压患者的差异基因。方法:用差别杂交法(Differentialhybridization)筛选正常人心脏cDNA文库的部分克隆,得到多个在自发性高血压鼠(SHR)心肌和高血压患者外周白细胞中高表达的线粒体基因。重组质粒,PCR-SSCP和测序,进行基因突变分析。结果:SHR鼠心肌线粒体ATPase6基因构象改变,8701位碱基由G→A(G8701A),编码的第59位氨基酸密码子由丙氨酸变成苏氨酸;A8708G,编码的第61位氨基酸由组氨酸变成精氨酸。高血压病患者外周血白细胞线粒体ATPase6基因8584位碱基突变(G8584A),编码的第20位氨基酸由丙氨酸变成苏氨酸,这一变化与SHR线粒体ATPase6基因改变相一致。结论:高血压病患者外用血白细胞线粒体ATPase6基因G8584A突变很可能在高血压病心肌肥厚的发生、发展中具有意义,并可能是高血压病的特异性改变。

关 键 词:高血压  线粒体  ATPase 6基因

Cloning, expression and mutation of mitochondrial ATPase gene of hypertensive patients and rats
Zhou Lin,Wan Dafang,Zhang Guoyuan,Li Hongnian,Zhang Pingping,Zhao Xintai,Gu Jianren,Liew C C. Cloning, expression and mutation of mitochondrial ATPase gene of hypertensive patients and rats[J]. Acta Academiae Medicinae Militaris Tertiae, 1999, 21(10): 729-733
Authors:Zhou Lin  Wan Dafang  Zhang Guoyuan  Li Hongnian  Zhang Pingping  Zhao Xintai  Gu Jianren  Liew C C
Affiliation:Zhou Lin, Wan Dafang, ZhangGuoyuan, Li Hongnian, Zhang Pingping, Zhao Xintai, Gu Jianren, Liew C C (ResearchInstitute of Field Surgery, Daping Hospital, Third Military Medical University,Chongqing,400042)
Abstract:Objective: To study the different expression of mitochondrial ATPase gene in normotensive and hypertensive human beings and rats. Methods: Partial cDNA clones were screened from human heart cDNA library with differential hybridization. Several mitochondrial genes were highly expressed in the DNA of the cardiac muscle of rats with spontaneous hypertension (SHRs) and in that of peripheral blood leukocytes of patients with hypertension. PCR-SSCP and sequencing were used to study the mutation of the genes.Results: There was polymorphism of mitochondrial ATPase 6 gene in the myocardium of SHR. The base of 8701 changed from G to A (G8701A) and the coden of 59 changed from alanine to threonine and the base of 8708 from A to G and the coden of 61 frorn histidine to arginine. The mitochondrial ATPase 6 gene in the leucocytes of hepertensive patients underwent simi1ar mutations of G8584A and from alanine to threonine in coden 20. Conclusion: The n1utation of G8584A in hypertensive patients is a specific change in hypertension and ! may be responsible for the initiation and development of myocardial hypertrophy.
Keywords:hypertension  mitochondrium  ATPase 6 gene  cloning  mutation  
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