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大肠杆菌1型菌毛表达相变控制的遗传分析。

Genetic analysis of the phase variation control of expression of type 1 fimbriae in Escherichia coli.

作者信息

Freitag C S, Abraham J M, Clements J R, Eisenstein B I

出版信息

J Bacteriol. 1985 May;162(2):668-75. doi: 10.1128/jb.162.2.668-675.1985.

DOI:10.1128/jb.162.2.668-675.1985
PMID:2859269
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC218902/
Abstract

Expression of type 1 fimbriae in Escherichia coli exhibits phase variation, whereby individual cells can alternate between states of organelle expression (Fim+) and nonexpression (Fim-). Strains with a fimD-lac operon fusion, in which lac, rather than fimD, expression is under the control of the fimD promoter, undergo Lac+ in equilibrium Lac- phase variation, instead. After positioning a lambda prophage adjacent to the operon fusion, we were able to isolate specialized lambda phage carrying both the fimD-lac fusion and the phase variation control region. Introduction of such phage into an Fim+ strain resulted in construction of a strain with a double, independently switching phenotype (Fim+ in equilibrium Fim- and Lac+ in equilibrium Lac-), demonstrating that the region controlling phase variation is contiguous with the fimD-lac operon fusion and is cis acting. When the specialized lambda phage was propagated on a delta lac delta fim strain, phase variation occurred within the plaques, confirming that the phase variation control region is carried on the specialized transducing phage. All lysogens acquired the Lac+ in equilibrium Lac- phenotype, except for two nonswitching Lac+ recombinants, which acquired Lac+ in equilibrium Lac- phase variation only by trans complementation with fim. Phase variation of type 1 fimbriae, therefore, appears to involve both a cis-active element, which is cloned on a specialized lambda phage, and a trans-active permissive factor, which is not present on the phage, but rather must be supplied by the recipient strain in the transduction.

摘要

大肠杆菌中1型菌毛的表达呈现相变,即单个细胞可在细胞器表达状态(Fim+)和不表达状态(Fim-)之间交替。带有fimD- lac操纵子融合的菌株,其中lac而非fimD的表达受fimD启动子控制,反而会经历Lac+与Lac-的平衡相变。在将λ原噬菌体定位到操纵子融合附近后,我们能够分离出携带fimD- lac融合和相变控制区域的特殊λ噬菌体。将这种噬菌体引入Fim+菌株导致构建出具有双重、独立切换表型的菌株(Fim+与Fim-平衡以及Lac+与Lac-平衡),这表明控制相变的区域与fimD- lac操纵子融合相邻且是顺式作用的。当特殊λ噬菌体在缺失lac和缺失fim的菌株上繁殖时,噬菌斑内会发生相变,证实相变控制区域由特殊转导噬菌体携带。除了两个不切换的Lac+重组体,所有溶原菌都获得了Lac+与Lac-平衡的表型,这两个重组体仅通过与fim的反式互补获得Lac+与Lac-平衡的相变。因此,1型菌毛的相变似乎涉及一个顺式活性元件,其克隆在特殊λ噬菌体上,以及一个反式活性许可因子,该因子不存在于噬菌体上,而是必须由转导中的受体菌株提供。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dda5/218902/ac381fd277cf/jbacter00222-0215-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dda5/218902/af8a9b6e2123/jbacter00222-0214-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dda5/218902/ac381fd277cf/jbacter00222-0215-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dda5/218902/af8a9b6e2123/jbacter00222-0214-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dda5/218902/ac381fd277cf/jbacter00222-0215-a.jpg

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