Burgers P M, Kornberg A, Sakakibara Y
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5391-5. doi: 10.1073/pnas.78.9.5391.
An Escherichia coli mutant, dnaN59, stops DNA synthesis promptly upon a shift to a high temperature; the wild-type dnaN gene carried in a transducing phage encodes a polypeptide of about 41,000 daltons [Sakakibara, Y. & Mizukami, T. (1980) Mol. Gen. Genet. 178, 541-553; Yuasa, S. & Sakakibara, Y. (1980) Mol. Gen. Genet. 180, 267-273]. We now find that the product of dnaN gene is the beta subunit of DNA polymerase III holoenzyme, the principal DNA synthetic multipolypeptide complex in E. coli. The conclusion is based on the following observations: (i) Extracts from dnaN59 cells were defective in phage phi X174 and G4 DNA synthesis after the mutant cells had been exposed to the increased temperature. (ii) The enzymatic defect was overcome by addition of purified beta subunit but not by other subunits of DNA polymerase III holoenzyme or by other replication proteins required for phi X174 DNA synthesis. (iii) Partially purified beta subunit from the dnaN mutant, unlike that from the wild type, was inactive in reconstituting the holoenzyme when mixed with the other purified subunits. (iv) Increased dosage of the dnaN gene provided by a plasmid carrying the gene raised cellular levels of the beta subunit 5- to 6-fold.
大肠杆菌突变体dnaN59在转移至高温后会迅速停止DNA合成;转导噬菌体携带的野生型dnaN基因编码一种约41,000道尔顿的多肽[Sakakibara, Y. & Mizukami, T. (1980) 《分子与普通遗传学》178, 541 - 553;Yuasa, S. & Sakakibara, Y. (1980) 《分子与普通遗传学》180, 267 - 273]。我们现在发现dnaN基因的产物是DNA聚合酶III全酶的β亚基,DNA聚合酶III全酶是大肠杆菌中主要的DNA合成多亚基复合体。这一结论基于以下观察结果:(i) 在突变细胞暴露于升高的温度后,来自dnaN59细胞的提取物在噬菌体φX174和G4 DNA合成方面存在缺陷。(ii) 添加纯化的β亚基可克服酶缺陷,但添加DNA聚合酶III全酶的其他亚基或φX174 DNA合成所需的其他复制蛋白则不能。(iii) 与野生型不同,来自dnaN突变体的部分纯化的β亚基在与其他纯化亚基混合时,在重组全酶方面无活性。(iv) 携带该基因的质粒提供的dnaN基因剂量增加使β亚基的细胞水平提高了5至6倍。