Kristensen T, Prydz H
Nucleic Acids Res. 1986 Mar 25;14(6):2597-609. doi: 10.1093/nar/14.6.2597.
Restriction analysis of DNA labelled with [32P]dCTP in an in vitro replication system with isolated nuclei from early S phase cells showed preferential labelling of restriction fragments derived from mitochondrial DNA (mtDNA) by a replication machinery distinct from that responsible for bulk nuclear DNA replication. Use of restriction nucleases with one recognition site in mtDNA gave rise to 16.5 kbp long fragments corresponding to full-length linearized mtDNA, indicating the presence of intact mtDNA in the isolated cell nuclei. Incorporation of dNTPs into mtDNA was not restricted to the S phase of the cell cycle. We were unable to increase the labelling of mtDNA by the addition of purified mitochondria or mtDNA to the nuclear replication system. These and other results presented is evidenced that the presence of mtDNA in the isolated nuclei was not due to uptake during preparation, thus indicating its presence in the cell nucleus in vivo.
在一个使用来自早S期细胞的分离细胞核的体外复制系统中,对用[32P]dCTP标记的DNA进行限制性分析,结果显示,一种不同于负责大量核DNA复制的复制机制,优先标记了源自线粒体DNA(mtDNA)的限制性片段。使用在mtDNA中具有一个识别位点的限制性核酸酶,产生了对应于全长线性化mtDNA的16.5 kbp长片段,表明在分离的细胞核中存在完整的mtDNA。dNTPs掺入mtDNA并不局限于细胞周期的S期。我们无法通过向核复制系统中添加纯化的线粒体或mtDNA来增加mtDNA的标记。本文呈现的这些及其他结果证明,分离细胞核中mtDNA的存在并非由于制备过程中的摄取,因此表明其在体内细胞核中的存在。