Sell S M, Eisen C, Ang D, Zylicz M, Georgopoulos C
Department of Cellular, Viral and Molecular Biology, University of Utah Medical Center, Salt Lake City 84132.
J Bacteriol. 1990 Sep;172(9):4827-35. doi: 10.1128/jb.172.9.4827-4835.1990.
Bacteriophage lambda requires the lambda O and P proteins for its DNA replication. The rest of the replication proteins are provided by the Escherichia coli host. Some of these host proteins, such as DnaK, DnaJ, and GrpE, are heat shock proteins. Certain mutations in the dnaK, dnaJ, or grpE gene block lambda growth at all temperatures and E. coli growth above 43 degrees C. We have isolated bacterial mutants that were shown by Southern analysis to contain a defective, mini-Tn10 transposon inserted into either of two locations and in both orientations within the dnaJ gene. We have shown that these dnaJ-insertion mutants did not grow as well as the wild type at temperatures above 30 degrees C, although they blocked lambda DNA replication at all temperatures. The dnaJ-insertion mutants formed progressively smaller colonies at higher temperatures, up to 42 degrees C, and did not form colonies at 43 degrees C. The accumulation of frequent, uncharacterized suppressor mutations allowed these insertion mutants to grow better at all temperatures and to form colonies at 43 degrees C. None of these suppressor mutations restored the ability of the host to propagate phage lambda. Radioactive labeling of proteins synthesized in vivo followed by immunoprecipitation or immunoblotting with anti-DnaJ antibodies demonstrated that no DnaJ protein could be detected in these mutants. Labeling studies at different temperatures demonstrated that these dnaJ-insertion mutations resulted in altered kinetics of heat shock protein synthesis. An additional eight dnaJ mutant isolates, selected spontaneously on the basis of blocking phage lambda growth at 42 degrees C, were shown not to synthesize DnaJ protein as well. Three of these eight spontaneous mutants had gross DNA alterations in the dnaJ gene. Our data provide evidence that the DnaJ protein is not absolutely essential for E. coli growth at temperatures up to 42 degrees C under standard laboratory conditions but is essential for growth at 43 degrees C. However, the accumulation of extragenic suppressors is necessary for rapid bacterial growth at higher temperatures.
λ噬菌体的DNA复制需要λO和P蛋白。其余的复制蛋白由大肠杆菌宿主提供。其中一些宿主蛋白,如DnaK、DnaJ和GrpE,是热休克蛋白。dnaK、dnaJ或grpE基因中的某些突变会在所有温度下阻止λ噬菌体生长,并在43摄氏度以上阻止大肠杆菌生长。我们分离出了细菌突变体,通过Southern分析表明,这些突变体含有一个缺陷型的mini-Tn10转座子,该转座子插入到dnaJ基因内的两个位置之一,且方向相反。我们已经表明,这些dnaJ插入突变体在30摄氏度以上的温度下生长不如野生型,尽管它们在所有温度下都能阻止λ噬菌体DNA复制。在高达42摄氏度的较高温度下,dnaJ插入突变体形成的菌落逐渐变小,在43摄氏度时不形成菌落。频繁出现的、未鉴定的抑制突变的积累使这些插入突变体在所有温度下生长得更好,并在43摄氏度时形成菌落。这些抑制突变均未恢复宿主繁殖λ噬菌体的能力。体内合成蛋白质的放射性标记,随后用抗DnaJ抗体进行免疫沉淀或免疫印迹,结果表明在这些突变体中检测不到DnaJ蛋白。在不同温度下的标记研究表明,这些dnaJ插入突变导致热休克蛋白合成动力学发生改变。另外八个基于在42摄氏度时阻止λ噬菌体生长而自发选择的dnaJ突变体分离株,也显示不能很好地合成DnaJ蛋白。这八个自发突变体中的三个在dnaJ基因中存在明显的DNA改变。我们的数据提供了证据,表明在标准实验室条件下,DnaJ蛋白对于大肠杆菌在高达42摄氏度的温度下生长并非绝对必需,但对于在43摄氏度时生长是必需的。然而,额外基因抑制子的积累对于细菌在较高温度下的快速生长是必要的。