Thaler D S, Stahl M M, Stahl F W
Genetics. 1987 Aug;116(4):501-11. doi: 10.1093/genetics/116.4.501.
The double-strand-break repair (DSBR) model was formulated to account for various aspects of yeast mitotic and meiotic recombination. In this study three features of the DSBR model are tested for Red-mediated recombination between phage lambda and lambda dv, a plasmid that is perfectly homologous to about 10% of lambda. The results support the applicability of the DSBR model to lambda's Red system: (1) Creating a double-strand-break (DSB) within the region of homology shared by phage and plasmid increases their genetic interaction by about 20-fold. A DSB outside the region of shared homology has no such effect. (2) Both patches, i.e., simple marker rescue, and splices, i.e., co-integration of the phage and plasmid, are stimulated by a DSB in the region of shared homology. (3) Co-integrants harbor a duplication of the region of shared homology. Among co-integrants that were formed by the creation of a DSB, there is a preferential loss of whichever allele was in cis to a utilized cut site. The DSBR model as originally formulated involves the isomerization and cleavage of Holliday junctions to resolve the canonical intermediate. We propose as an alternative mechanism that a topoisomerase can resolve the canonical DSBR intermediate.
双链断裂修复(DSBR)模型的提出是为了解释酵母有丝分裂和减数分裂重组的各个方面。在本研究中,针对噬菌体λ与λdv(一种与λ约10%完全同源的质粒)之间的Red介导重组,对DSBR模型的三个特征进行了测试。结果支持DSBR模型适用于λ的Red系统:(1)在噬菌体和质粒共享的同源区域内产生双链断裂(DSB)可使它们的遗传相互作用增加约20倍。共享同源区域外的DSB则没有这种效果。(2)共享同源区域内的DSB会刺激斑块(即简单标记拯救)和拼接(即噬菌体和质粒的共整合)。(3)共整合体含有共享同源区域的重复序列。在通过产生DSB形成的共整合体中,与所用切割位点顺式排列的任何等位基因都有优先丢失的情况。最初提出的DSBR模型涉及霍利迪连接体的异构化和切割以解析标准中间体。我们提出一种替代机制,即拓扑异构酶可以解析标准的DSBR中间体。