Albertini A M, Hofer M, Calos M P, Miller J H
Cell. 1982 Jun;29(2):319-28. doi: 10.1016/0092-8674(82)90148-9.
Using lacl-Z fusion strains of Escherichia coli we have devised systems that detect deletions of varying lengths. We examined deletions 700-1000 base pairs long, and genetically characterized over 250 spontaneous deletions. Of these, we analyzed 24 by direct DNA sequencing and 18 by inspection of restriction fragment patterns. Deletions of this size occur almost exclusively at short repeated sequences in both (recA+ and recA- strain backgrounds, but are detected 25-fold more frequently in a recA+ background. The frequency of deletion formation correlates with the extent of homology between the short repeated sequences, although other factors may be involved. The largest hotspot, which accounts for 60% of the deletions detected, involves the largest homology in the system (14 of 17 base pairs). Altering a single base pair within this homology reduces deletion incidence by an order of magnitude. We discuss possible mechanisms of deletion formation and consider its relationship to the excision of transposable elements.
利用大肠杆菌的乳糖操纵子-Z融合菌株,我们设计了能检测不同长度缺失的系统。我们研究了长度为700-1000个碱基对的缺失,并对250多个自发缺失进行了遗传学特征分析。其中,我们通过直接DNA测序分析了24个,通过检查限制性片段模式分析了18个。这种大小的缺失几乎只发生在(recA+和recA-菌株背景中的)短重复序列处,但在recA+背景中检测到的频率要高25倍。缺失形成的频率与短重复序列之间的同源程度相关,不过可能还涉及其他因素。最大的热点区域占检测到的缺失的60%,涉及系统中最大的同源性(17个碱基对中的14个)。改变该同源性内的单个碱基对会使缺失发生率降低一个数量级。我们讨论了缺失形成的可能机制,并考虑了其与转座元件切除的关系。