Wong T W, Clayton D A
Cell. 1985 Oct;42(3):951-8. doi: 10.1016/0092-8674(85)90291-0.
Synthesis of human light-strand mitochondrial DNA was accomplished in vitro using DNA primase, DNA polymerase, and other accessory proteins isolated from human mitochondria. Replication begins with the synthesis of primer RNA on a T-rich sequence in the origin stem-loop structure of the template DNA and absolutely requires ATP. A transition from RNA synthesis to DNA synthesis occurs near the base of the stem-loop structure and a potential recognition site for signaling that transition has been identified. The start sites of the in vitro products were mapped at the nucleotide level and were found to be in excellent agreement with those of in vivo nascent light-strand DNA. Isolated human mitochondrial enzymes recognize and utilize the bovine, but not the mouse, origin of light-strand replication.
利用从人线粒体中分离出的DNA引发酶、DNA聚合酶及其他辅助蛋白,在体外完成了人轻链线粒体DNA的合成。复制起始于模板DNA的起始茎环结构中富含T的序列上引物RNA的合成,且绝对需要ATP。从RNA合成到DNA合成的转变发生在茎环结构的基部附近,并且已鉴定出一个用于信号传导该转变的潜在识别位点。体外产物的起始位点在核苷酸水平上进行了定位,发现与体内新生轻链DNA的起始位点高度一致。分离出的人线粒体酶识别并利用牛的轻链复制起始位点,但不利用小鼠的。