Melendy T, Sheline C, Ray D S
Molecular Biology Institute, University of California, Los Angeles 90024.
Cell. 1988 Dec 23;55(6):1083-8. doi: 10.1016/0092-8674(88)90252-8.
A type II DNA topoisomerase (topollmt), purified to near homogeneity from the trypanosomatid C. fasciculata has been shown to be localized to the single mitochondrion of these kinetoplastid protozoa. Immunoblots show at least a 10-fold higher level of topollmt (per milligram of protein) in preparations of partially purified mitochondria as compared with those from whole cells. Analyses of type I and type II topoisomerase activities in both mitochondrial and whole cell extracts show a 4- to 5-fold higher specific activity of topollmt in mitochondrial extracts while a nuclear type I topoisomerase has a 4- to 5-fold lower specific activity in the same extract. Immunolocalizations using anti-topollmt antibodies show the enzyme to be present in close association with the mitochondrial DNA networks (kinetoplast DNA or kDNA). This association appears at two distinct locations on opposite sides of the kDNA network.
从锥虫类生物克氏锥虫中纯化至近乎同质的II型DNA拓扑异构酶(topollmt)已被证明定位于这些动质体原生动物的单个线粒体中。免疫印迹显示,与全细胞提取物相比,部分纯化的线粒体提取物中topollmt(每毫克蛋白质)的水平至少高10倍。对线粒体和全细胞提取物中I型和II型拓扑异构酶活性的分析表明,线粒体提取物中topollmt的比活性高4至5倍,而核I型拓扑异构酶在相同提取物中的比活性低4至5倍。使用抗topollmt抗体的免疫定位显示该酶与线粒体DNA网络(动质体DNA或kDNA)紧密相关。这种关联出现在kDNA网络相对两侧的两个不同位置。