Shapiro J A, Higgins N P
Department of Biochemistry and Molecular Biology, University of Chicago, Illinois 60637.
J Bacteriol. 1989 Nov;171(11):5975-86. doi: 10.1128/jb.171.11.5975-5986.1989.
In Escherichia coli colonies, patterns of differential gene expression can be visualized by the use of Mu d(lac) fusion elements. Here we report that patterned beta-galactosidase expression in colonies of strain MS1534 resulted from a novel mechanism, spatially localized replication of the Mu dII1681 element causing lacZ transposition to active expression sites. Mu dII1681 replication did not occur constitutively with a fixed probability but was dependent on the growth history of the bacterial population. The bacteria in which Mu dII1681 replication and lacZ transposition had occurred could no longer form colonies. These results lead to several interesting conclusions about cellular differentiation during colony development and the influence of bacterial growth history on gene expression and genetic change.
在大肠杆菌菌落中,通过使用Mu d(lac)融合元件可以观察到差异基因表达模式。在此我们报告,MS1534菌株菌落中β-半乳糖苷酶的模式化表达源自一种新机制,即Mu dII1681元件的空间定位复制导致lacZ转座至活性表达位点。Mu dII1681的复制并非以固定概率持续发生,而是取决于细菌群体的生长历史。发生了Mu dII1681复制和lacZ转座的细菌不再能够形成菌落。这些结果得出了几个关于菌落发育过程中细胞分化以及细菌生长历史对基因表达和遗传变化影响的有趣结论。