Glasunov A, Frankenberg-Schwager M, Frankenberg D
Institute for Genetics of Industrial Microorganisms, Moscow, Russia.
Mol Gen Genet. 1995 Apr 10;247(1):55-60. doi: 10.1007/BF00425821.
In this paper we study the influence of non-homology between plasmid and chromosomal DNA on the efficiency of recombinational repair of plasmid double-strand breaks and gaps in yeast. For this purpose we used different combinations of plasmids and yeast strains carrying various deletions within the yeast LYS2 gene. A 400 bp deletion in plasmid DNA had no effect on recombinational plasmid repair. However, a 400 bp deletion in chromosomal DNA dramatically reduced the efficiency of this repair mechanism, but recombinational repair of plasmids linearized by a double-strand break with cohesive ends still remained the dominant repair process. We have also studied the competition between recombination and ligation in the repair of linearized plasmids. Our experimental evidence suggests that recombinational repair is attempted but aborted if only one recombinogenic end with homology to chromosomal DNA is present in plasmid DNA. This situation results in a decreased probability of non-recombinational (i.e. ligation) repair of linearized plasmid DNA.
在本文中,我们研究了质粒与染色体DNA之间的非同源性对酵母中质粒双链断裂和缺口的重组修复效率的影响。为此,我们使用了携带酵母LYS2基因内各种缺失的质粒和酵母菌株的不同组合。质粒DNA中的400 bp缺失对质粒的重组修复没有影响。然而,染色体DNA中的400 bp缺失显著降低了这种修复机制的效率,但具有粘性末端的双链断裂线性化质粒的重组修复仍然是主要的修复过程。我们还研究了线性化质粒修复过程中重组与连接之间的竞争。我们的实验证据表明,如果质粒DNA中仅存在一个与染色体DNA具有同源性的重组末端,则会尝试进行重组修复但会中止。这种情况导致线性化质粒DNA非重组(即连接)修复的概率降低。