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线粒体肌病中线粒体DNA缺失的组织分布与传播

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.

作者信息

Zeviani M, Gellera C, Pannacci M, Uziel G, Prelle A, Servidei S, DiDonato S

机构信息

Department of Biochemistry and Genetics, Istituto Nazionale Neurologico, Carlo Besta, Milan, Italy.

出版信息

Ann Neurol. 1990 Jul;28(1):94-7. doi: 10.1002/ana.410280118.

Abstract

By using a combination of Southern blot hybridization analysis, polymerase-chain reaction amplification, and direct nucleotide sequencing, we studied deletions of mitochondrial DNA (mtDNA) in several nonfamilial patients with progressive external ophthalmoplegia and Kearns-Sayre syndrome, and in some of their direct relatives. Results suggest that the heteroplasmic mtDNA populations are already present at a very early stage of development, and that there is no direct transmission of mtDNA heteroplasmy by maternal inheritance.

摘要

通过结合Southern印迹杂交分析、聚合酶链反应扩增和直接核苷酸测序,我们研究了几名患有进行性眼外肌麻痹和卡恩斯-塞尔综合征的非家族性患者及其一些直系亲属中线粒体DNA(mtDNA)的缺失情况。结果表明,异质性mtDNA群体在发育的非常早期阶段就已存在,并且mtDNA异质性不会通过母系遗传直接传递。

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