Harris R S, Ross K J, Rosenberg S M
Department of Biological Sciences, University of Alberta, Edmonton, Canada.
Genetics. 1996 Mar;142(3):681-91. doi: 10.1093/genetics/142.3.681.
Aspects of the molecular mechanism of "adaptive" mutation are emerging from one experimental system: reversion of an Escherichia coli lac frameshift mutation carried on a conjugative plasmid. Homologous recombination is required and the mutations resemble polymerase errors. Reports implicating a role for conjugal transfer proteins suggested that the mutation mechanism is ordinary replication error occurring during transfer synthesis, followed by conjugation-like recombination, to capture the replicated fragment into an intact replicon. Whereas conjugational recombination uses either of two systems of Holliday junction resolution, we find that the adaptive lac reversions are inhibited by one resolution system and promoted by the other. Moreover, temporary absence of both resolution systems promotes mutation. These results imply that recombination intermediates themselves promote the mutations.
“适应性”突变的分子机制的一些方面正从一个实验系统中显现出来:携带在接合质粒上的大肠杆菌乳糖移码突变的回复。同源重组是必需的,并且这些突变类似于聚合酶错误。涉及接合转移蛋白作用的报告表明,突变机制是在转移合成过程中发生的普通复制错误,随后是类似接合的重组,以将复制片段捕获到完整的复制子中。虽然接合重组使用两种Holliday连接点解析系统中的任何一种,但我们发现适应性乳糖回复被一种解析系统抑制而被另一种促进。此外,两种解析系统的暂时缺失会促进突变。这些结果表明重组中间体本身促进了突变。