Stupina Vera A, Wang James C
Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
J Biol Chem. 2005 Jan 7;280(1):355-60. doi: 10.1074/jbc.M411924200. Epub 2004 Nov 1.
The viability of the topA mutants lacking DNA topoisomerase I was thought to depend on the presence of compensatory mutations in Escherichia coli but not Salmonella typhimurium or Shigella flexneri. This apparent discrepancy in topA requirements in different bacteria prompted us to reexamine the topA requirements in E. coli. We find that E. coli strains bearing topA mutations, introduced into the strains by DNA-mediated gene replacement, are viable at 37 or 42 degrees C without any compensatory mutations. These topA(-) cells exhibit cold sensitivity in their growth, however, and this cold sensitivity phenotype appears to be caused by excessive negative supercoiling of intracellular DNA. In agreement with previous results (Zhu, Q., Pongpech, P., and DiGate, R. J. (2001) Proc. Natl. Acad. Sci. U. S. A. 98, 9766-9771), E. coli cells lacking both type IA DNA topoisomerases I and III are found to be nonviable, indicating that the two type IA enzymes share a critical cellular function.
缺乏DNA拓扑异构酶I的topA突变体的生存能力被认为取决于大肠杆菌中补偿性突变的存在,而鼠伤寒沙门氏菌或福氏志贺氏菌中则不存在这种情况。不同细菌对topA需求的这种明显差异促使我们重新审视大肠杆菌中对topA的需求。我们发现,通过DNA介导的基因置换引入菌株的携带topA突变的大肠杆菌菌株,在37或42摄氏度下无需任何补偿性突变即可存活。然而,这些topA(-)细胞在生长过程中表现出冷敏感性,这种冷敏感性表型似乎是由细胞内DNA过度负超螺旋引起的。与先前的结果一致(朱,Q.,蓬佩奇,P.,和迪盖特,R.J.(2001年)美国国家科学院院刊98,9766 - 9771),发现同时缺乏IA型DNA拓扑异构酶I和III的大肠杆菌细胞无法存活,这表明这两种IA型酶共享关键的细胞功能。