Carpenter L R, Englund P T
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Mol Cell Biol. 1995 Dec;15(12):6794-803. doi: 10.1128/MCB.15.12.6794.
Kinetoplast DNA, the mitochondrial DNA of trypanosomatids, is composed of several thousand minicircles and a few dozen maxicircles, all of which are topologically interlocked in a giant network. We have studied the replication of maxicircle DNA, using electron microscopy to analyze replication intermediates from both Crithidia fasciculata and Trypanosoma brucei. Replication intermediates were stabilized against branch migration by introducing DNA interstrand cross-links in vivo with 4,5',8-trimethylpsoralen and UV radiation. Electron microscopy of individual maxicircles resulting from a topoisomerase II decatenation of kinetoplast DNA networks revealed intact maxicircle theta structures. Analysis of maxicircle DNA linearized by restriction enzyme cleavage revealed branched replication intermediates derived from theta structures. Measurements of the linearized branched molecules in both parasites indicate that replication initiates in the variable region (a noncoding segment characterized by repetitive sequences) and proceeds unidirectionally, clockwise on the standard map.
动质体DNA是锥虫的线粒体DNA,由数千个微小环和几十条大环组成,所有这些都在一个巨大的网络中拓扑互锁。我们利用电子显微镜分析来自罗得西亚锥虫和布氏锥虫的复制中间体,研究了大环DNA的复制。通过在体内用4,5',8-三甲基补骨脂素和紫外线辐射引入DNA链间交联,使复制中间体免受分支迁移的影响。对动质体DNA网络进行拓扑异构酶II解连环作用后得到的单个大环进行电子显微镜观察,发现了完整的大环θ结构。对经限制性内切酶切割线性化的大环DNA的分析揭示了源自θ结构的分支复制中间体。对两种寄生虫中线性化分支分子的测量表明,复制起始于可变区(一个以重复序列为特征的非编码区段),并沿标准图谱顺时针单向进行。