Kuchta Robert D, Stengel Gudrun
Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309, USA.
Biochim Biophys Acta. 2010 May;1804(5):1180-9. doi: 10.1016/j.bbapap.2009.06.011. Epub 2009 Jun 21.
DNA primase synthesizes short RNA primers that replicative polymerases further elongate in order to initiate the synthesis of all new DNA strands. Thus, primase owes its existence to the inability of DNA polymerases to initiate DNA synthesis starting with 2 dNTPs. Here, we discuss the evolutionary relationships between the different families of primases (viral, eubacterial, archael, and eukaryotic) and the catalytic mechanisms of these enzymes. This includes how they choose an initiation site, elongate the growing primer, and then only synthesize primers of defined length via an inherent ability to count. Finally, the low fidelity of primases along with the development of primase inhibitors is described.
DNA引发酶合成短的RNA引物,复制性聚合酶会进一步延长这些引物,以起始所有新DNA链的合成。因此,引发酶的存在归因于DNA聚合酶无法以两个脱氧核苷酸三磷酸(dNTP)起始DNA合成。在此,我们讨论不同家族引发酶(病毒、真细菌、古细菌和真核生物)之间的进化关系以及这些酶的催化机制。这包括它们如何选择起始位点、延长正在生长的引物,然后通过固有的计数能力仅合成特定长度的引物。最后,描述了引发酶的低保真性以及引发酶抑制剂的发展情况。