Hixson J E, Wong T W, Clayton D A
J Biol Chem. 1986 Feb 15;261(5):2384-90.
Mammalian mitochondrial DNAs contain a conserved origin of light-strand replication that supports accurate initiation of DNA synthesis in vitro. This provides an opportunity to examine the sequence requirements for initiation through in vitro analysis of a series of deleted and mutagenized DNA templates. These assays use enzymes isolated from human mitochondria and single-stranded DNA templates containing deletions or substitutions in the known origin region. The data indicate that accurate and efficient light-strand replication in vitro requires the previously identified stem-loop structure located within a tRNA cluster. In addition, the template sequence 3'-GGCCG-5', located immediately adjacent to the stem, is necessary for efficient replication. This sequence, the complement of which encodes the 3' end of tRNACys, may be the site of transition from RNA primer synthesis to DNA synthesis. Surprisingly, substitutions within a region located in the loop of this origin do not reduce levels of replication.
哺乳动物线粒体DNA含有一个保守的轻链复制起点,该起点支持体外DNA合成的精确起始。这提供了一个机会,通过对一系列缺失和诱变的DNA模板进行体外分析,来研究起始的序列要求。这些实验使用从人线粒体中分离的酶和在已知起点区域含有缺失或取代的单链DNA模板。数据表明,体外精确且高效的轻链复制需要位于tRNA簇内的先前鉴定的茎环结构。此外,紧邻茎的模板序列3'-GGCCG-5'对于高效复制是必需的。该序列的互补序列编码tRNACys的3'末端,可能是从RNA引物合成过渡到DNA合成的位点。令人惊讶的是,该起点环内区域的取代并不会降低复制水平。