Schumacher S, Fuchs R P, Bichara M
Cancérogénèse et Mutagénèse Moléculaire et Structurale, UPR 9003, CNRS, Strasbourg-Illkirch, France.
J Bacteriol. 1997 Oct;179(20):6512-7. doi: 10.1128/jb.179.20.6512-6517.1997.
In Escherichia coli, (GpC)n sequences cloned into plasmid DNA molecules are deletion-prone with the occurrence of both short (<2 bp) and long (>2 bp) deletion events. These repetitive tracts can be stabilized by interrupting the strict monotony of the repetition with a variant dinucleotide sequence. The stabilization of short deletion events that is mediated by the variant sequence is completely lost in E. coli mismatch repair-deficient strains. In contrast, this repair pathway has no influence on the frequency of occurrence of long deletion events, even in sequences containing the variant repeat. These results lead us to propose two distinct models to account for short and long deletions within repetitive sequences in E. coli. Furthermore, this study reveals that the deletions occur preferentially at the end of the repeat sequence that is distal with respect to the origin of replication.
在大肠杆菌中,克隆到质粒DNA分子中的(GpC)n序列容易发生缺失,会出现短(<2 bp)和长(>2 bp)缺失事件。通过用可变二核苷酸序列打断重复的严格单调性,可以使这些重复序列稳定下来。由可变序列介导的短缺失事件的稳定在大肠杆菌错配修复缺陷菌株中完全丧失。相比之下,即使在含有可变重复序列的序列中,这种修复途径对长缺失事件的发生频率也没有影响。这些结果使我们提出两个不同的模型来解释大肠杆菌中重复序列内的短缺失和长缺失。此外,这项研究表明,缺失优先发生在相对于复制起点较远的重复序列末端。