Arezi B, Kirk B W, Copeland W C, Kuchta R D
Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, USA.
Biochemistry. 1999 Sep 28;38(39):12899-907. doi: 10.1021/bi9908991.
Regulation of the p49-p58 primase complex during primer synthesis and the interaction of the primase subunits with DNA were examined. After primase synthesizes a primer that DNA polymerase alpha (pol alpha) can readily elongate, further primase activity is negatively regulated. This occurs within both the context of the four-subunit pol alpha-primase complex and in the p49-p58 primase complex, indicating that the newly generated primer-template species need not interact with pol alpha to regulate further primase activity. Photo-cross-linking of single-stranded DNA-primase complexes revealed that whereas the isolated p49 and p58 subunits both reacted with DNA upon photolysis, only the p58 subunit reacted with the DNA when photolysis was performed using the p49-p58 primase complex. After primer synthesis by the complex, p58 was again the only subunit that reacted with the DNA. These results suggest a model for regulation of primer synthesis in which the newly synthesized primer-template species binds to p58 and regulates further primer synthesis. Additionally, the ability of p58 to interact with primer-template species suggests that p58 mediates the transfer of primers from the primase active site to pol alpha.
研究了引物合成过程中p49 - p58引发酶复合物的调控以及引发酶亚基与DNA的相互作用。在引发酶合成出DNA聚合酶α(polα)能够轻易延伸的引物后,进一步的引发酶活性受到负调控。这在四亚基polα - 引发酶复合物以及p49 - p58引发酶复合物的背景下均会发生,表明新生成的引物 - 模板物种无需与polα相互作用即可调控进一步的引发酶活性。单链DNA - 引发酶复合物的光交联显示,虽然分离的p49和p58亚基在光解时均与DNA发生反应,但当使用p49 - p58引发酶复合物进行光解时,只有p58亚基与DNA发生反应。复合物合成引物后,p58再次成为唯一与DNA发生反应的亚基。这些结果提示了一种引物合成调控模型,即新合成的引物 - 模板物种与p58结合并调控进一步的引物合成。此外,p58与引物 - 模板物种相互作用的能力表明p58介导了引物从引发酶活性位点向polα的转移。