Kaguni L S, Clayton D A
Proc Natl Acad Sci U S A. 1982 Feb;79(4):983-7. doi: 10.1073/pnas.79.4.983.
The activity of Drosophila melanogaster DNA polymerase alpha on DNA-primed single-stranded DNA templates has been examined. The DNA templates contain a 1471-nucleotide sequence from the heavy-strand origin region of mouse mtDNA inserted into the single-stranded bacteriophage vector M13Gori1. Preferred sites for pausing of in vitro DNA synthesis have been mapped within the cloned mtDNA insert and in the G4 cDNA strand origin which is contained within the vector DNA. Analysis of nascent DNA strands from replicative intermediates has revealed that pause sites are discrete and lie both at the positions of predicted stable dyads and in regions lacking the potential for formation of such structures. The patterns of kinetic pause sites observed for Escherichia coli DNA polymerase III holoenzyme is qualitatively similar to that found for DNA polymerase alpha. A subset of the observed kinetic pause signals are recognized by E. coli DNA polymerase I under similar conditions.
已对果蝇DNA聚合酶α在以DNA为引物的单链DNA模板上的活性进行了检测。DNA模板包含一段来自小鼠线粒体DNA重链起始区域的1471个核苷酸序列,该序列插入到单链噬菌体载体M13Gori1中。体外DNA合成暂停的优选位点已在克隆的线粒体DNA插入片段内以及载体DNA中所含的G4 cDNA链起始部位进行了定位。对复制中间体新生DNA链的分析表明,暂停位点是离散的,既位于预测的稳定二分体位置,也位于缺乏形成此类结构潜力的区域。观察到的大肠杆菌DNA聚合酶III全酶的动力学暂停位点模式与DNA聚合酶α的模式在质量上相似。在类似条件下,大肠杆菌DNA聚合酶I可识别一部分观察到的动力学暂停信号。