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线粒体DNA拷贝数极低的人类细胞突变体(ρ°细胞)

Human cell mutants with very low mitochondrial DNA copy number (rho d).

作者信息

Vaillant F, Nagley P

机构信息

Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australia.

出版信息

Hum Mol Genet. 1995 May;4(5):903-14. doi: 10.1093/hmg/4.5.903.

Abstract

Mutants of human Namalwa cells are described, denoted rho d (mtDNA-depleted), which contain a very low mtDNA copy number. Three isolates, denoted FV02, FV03 and FV05, each selected on the basis of their pyruvate-dependent phenotype, were shown to have severely reduced mitochondrial respiratory functions consistent with results of histochemical and cytochrome analysis. Analyses of mtDNA by the polymerase chain reaction (PCR) and Southern blotting indicated that FV02, FV03 and FV05 each contained a full complement of mtDNA sequences, 16.6 kb in length, in circular form but at a greatly reduced level compared with that of parent rho + cells. Quantitative PCR tests showed first, that the parent Namalwa rho + cells contain about 1800 molecules of mtDNA and second, that cells of each of FV02, FV03 and FV05 contain between 100- and 1000-fold less mtDNA than rho + cells. Subclones of each of FV02, FV03 and FV05 all contained detectable mtDNA, thus eliminating the possibility that these isolates are mixtures of rho o (devoid of mtDNA) and rho + cells. Each of the rho d cell lines FV02, FV03 and FV05 had a more rapid growth rate than the corresponding rho o cells but less than that of the parent Namalwa rho + cells. The experimentally induced rho d cells described here may represent a useful model for human diseases in which severe depletion of cellular mtDNA levels in tissues is encountered.

摘要

本文描述了人Namalwa细胞的突变体,命名为rho d(线粒体DNA缺失型),其线粒体DNA拷贝数极低。基于丙酮酸依赖表型筛选出的三个分离株,分别命名为FV02、FV03和FV05,经检测发现它们的线粒体呼吸功能严重受损,这与组织化学和细胞色素分析结果一致。通过聚合酶链反应(PCR)和Southern印迹法对线粒体DNA进行分析,结果表明FV02、FV03和FV05均含有完整的线粒体DNA序列,呈环状,长度为16.6 kb,但与亲本rho +细胞相比,其含量大幅降低。定量PCR检测结果显示,首先,亲本Namalwa rho +细胞含有约1800个线粒体DNA分子;其次,FV02、FVOS和FV05的细胞线粒体DNA含量比rho +细胞少100至1000倍。FV02、FV03和FV05的每个亚克隆均含有可检测到的线粒体DNA,因此排除了这些分离株是rho o(不含线粒体DNA)和rho +细胞混合物的可能性。rho d细胞系FV02、FV03和FV05的生长速度均比相应的rho o细胞快,但比亲本Namalwa rho +细胞慢。本文所描述的实验诱导产生的rho d细胞可能是一种有用的模型,可用于研究那些在组织中细胞线粒体DNA水平严重降低的人类疾病。

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