冠心病患者线粒体细胞色素C氧化酶亚基Ⅱ基因片段的重排
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The Rearrangement in Mitochondrial Cytochrome C Oxidase Subunit Ⅱ Gene and Coronary Heart Disease
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    摘要:

    采用玻璃粉微量吸附法获取DNA直接作为PCR反应的模板,利用巢式PCR技术,检测冠心病患者血细胞内编码细胞色素C氧化酶亚基Ⅱ的线粒体DNA扩增片段多态性,探讨线粒体DNA的片段缺失与动脉粥样硬化发生发展的关系。研究发现在全部冠心病患者编码细胞色素C氧化酶亚基Ⅱ的基因中出现了大约10 0bp的缺失片段,其中1例冠心病患者中还出现了大约45 0bp核基因组和6 0 0bp的线粒体DNA扩增片段,而在正常对照老人中没有出现片段的重排现象。表明冠心病患者中存在该基因片段的缺失和模板量减少的现象,该基因可能参与了冠状动脉粥样硬化的形成与发展,编码呼吸链复合物一些亚基线粒体DNA片段的重排可能是动脉粥样硬化进行性发展的恶化因素。

    Abstract:

    Aim To explore the relationship between the pathogenesis of coronary heart disease and the rearrangement in the mitochondrial DNA(mtDNA). Methods and Results Traced mtDNA was adsorbed by glass milk method and was taken as the templet DNA of PCR directly. The nest PCR was used to test 100 bp corresponding to deleted mitochondrial DNA and was detected in five patients with coronary heart disease. A short fragment of approximately 600 bp correspondeding inserted mitochondrial DNA was detected in one patient with coronary heart disease. These didn't appear in the normals. Another short fragment of approximately 450 bp corresponded to human nucleic genome. Conclusion The mitochondrial CO2 gene may be linked to the pathogenesis of coronary heart disease. The length mutations of the mtDNA that encodes several subunits of the respiratory chain complexes contribute to the depravation of some forms of atherosclerosis.

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邱小忠,陈瑗,周玫.冠心病患者线粒体细胞色素C氧化酶亚基Ⅱ基因片段的重排[J].中国动脉硬化杂志,2001,9(2):131~133.

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  • 收稿日期:2000-10-08
  • 最后修改日期:2001-04-16
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