Henson J M, Chu H, Irwin C A, Walker J R
Genetics. 1979 Aug;92(4):1041-59. doi: 10.1093/genetics/92.4.1041.
Escherichia coli mutants with temperature-sensitive (ts) mutations in dnaX and dnaY genes have been isolated. Based on transduction by phage P1, dnaX and Y have been mapped at minutes 10.4--10.5 and 12.1, respectively, in the sequence dnaX purE dnaY. Both dna Xts36 and Yts10 are recessive to wild-type alleles present on episomes. F13 carries both dnaX+ and Y+; the shorter F210 carries dnaY+, but not X+. Lambda tranducing phages that carry dnaX+ or Y+ have been isolated, and hybrid plasmids of Col E1 and E. coli DNA from the Clarke and Carbon (1976) collection also carry portions of the dnaX purE dnaY region. Results obtained with the lambda transducing phages and the hybrid plasmids suggest that dnaX is a different gene from the previously characterized dnaZ gene, which is also near minute 10.5--The dnaXts36 mutant, after a shift to 42 degrees, stopped DNA synthesis gradually, and the total amount of DNA increased two-fold. When this mutant was shifted to 44 degrees, the rate of DNA synthesis dropped immediately and the final increment of DNA was only 10% of the initial amount. Replicative DNA synthesis in toluene-treated cells was completely inhibited at 42 degrees and was partially inhibited even at 30 degrees.--When the dnaYts10 mutant was shifted to 42 degrees, DNA synthesis gradually stopped, and the amount of DNA increased 3.6-fold. At 44 degrees, residual DNA synthesis amounted to a two-fold increase. Replicative DNA synthesis in vitro in toluene-treated cells was inactivated after 20 minutes at 42 degrees or by "preincubation" of cells at 42 degrees before toluene treatment.--The dnaX and dnaY products probably function in polymerization of DNA, although participation also in initiation cannot be excluded.
已分离出在dnaX和dnaY基因中存在温度敏感(ts)突变的大肠杆菌突变体。基于噬菌体P1的转导,dnaX和Y分别定位在序列dnaX purE dnaY中10.4 - 10.5分钟和12.1分钟处。dnaXts36和Yts10对附加体上存在的野生型等位基因均为隐性。F13同时携带dnaX +和Y +;较短的F210携带dnaY +,但不携带X +。已分离出携带dnaX +或Y +的λ转导噬菌体,并且来自克拉克和卡尔文(1976年)文库的Col E1和大肠杆菌DNA的杂交质粒也携带dnaX purE dnaY区域的部分片段。用λ转导噬菌体和杂交质粒获得的结果表明,dnaX是一个与先前鉴定的dnaZ基因不同的基因,dnaZ基因也在10.5分钟附近。dnaXts36突变体在转移到42℃后,DNA合成逐渐停止,DNA总量增加了两倍。当该突变体转移到44℃时,DNA合成速率立即下降,DNA的最终增量仅为初始量的10%。经甲苯处理的细胞中的复制性DNA合成在42℃时完全被抑制,甚至在30℃时也被部分抑制。当dnaYts10突变体转移到42℃时,DNA合成逐渐停止,DNA量增加了3.6倍。在44℃时,残余的DNA合成增加了两倍。经甲苯处理的细胞在42℃下20分钟后或在甲苯处理前在42℃下“预孵育”后,体外复制性DNA合成失活。dnaX和dnaY产物可能在DNA聚合中起作用,尽管也不能排除参与起始过程。