Maul Robert W, Sanders Laurie H, Lim James B, Benitez Rosemary, Sutton Mark D
Department of Biochemistry, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, 3435 Main Street, Buffalo, NY 14214, USA.
J Bacteriol. 2007 Jul;189(13):4688-95. doi: 10.1128/JB.00476-07. Epub 2007 Apr 20.
The Escherichia coli dnaN159 allele encodes a mutant form of the beta-sliding clamp (beta159) that is impaired for interaction with the replicative DNA polymerase (Pol), Pol III. In addition, strains bearing the dnaN159 allele require functional Pol I for viability. We have utilized a combination of genetic and biochemical approaches to characterize the role(s) played by Pol I in the dnaN159 strain. Our findings indicate that elevated levels of Pol I partially suppress the temperature-sensitive growth phenotype of the dnaN159 strain. In addition, we demonstrate that the beta clamp stimulates the processivity of Pol I in vitro and that beta159 is impaired for this activity. The reduced ability of beta159 to stimulate Pol I in vitro correlates with our finding that single-stranded DNA (ssDNA) gap repair is impaired in the dnaN159 strain. Taken together, these results suggest that (i) the beta clamp-Pol I interaction may be important for proper Pol I function in vivo and (ii) in the absence of Pol I, ssDNA gaps may persist in the dnaN159 strain, leading to lethality of the dnaN159 DeltapolA strain.
大肠杆菌dnaN159等位基因编码β滑动夹(β159)的一种突变形式,该突变形式与复制性DNA聚合酶(Pol)Pol III的相互作用受损。此外,携带dnaN159等位基因的菌株需要功能性的Pol I才能存活。我们利用遗传学和生物化学方法相结合来表征Pol I在dnaN159菌株中所起的作用。我们的研究结果表明,Pol I水平的升高部分抑制了dnaN159菌株的温度敏感生长表型。此外,我们证明β夹在体外刺激Pol I的持续合成能力,并且β159在该活性方面受损。β159在体外刺激Pol I的能力降低与我们的发现相关,即dnaN159菌株中的单链DNA(ssDNA)缺口修复受损。综上所述,这些结果表明:(i)β夹与Pol I的相互作用对于Pol I在体内的正常功能可能很重要;(ii)在没有Pol I的情况下,dnaN159菌株中可能会持续存在ssDNA缺口,导致dnaN159 DeltapolA菌株死亡。