Vallet-Gely Isabelle, Donovan Katherine E, Fang Rui, Joung J Keith, Dove Simon L
Division of Infectious Diseases, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2005 Aug 2;102(31):11082-7. doi: 10.1073/pnas.0502663102. Epub 2005 Jul 25.
The cupA gene cluster of Pseudomonas aeruginosa encodes components of a putative fimbrial structure that enable this opportunistic human pathogen to form biofilms on abiotic surfaces. In P. aeruginosa, cupA gene expression is repressed by MvaT, a putative transcription regulator thought to belong to the H-NS family of nucleoid-associated proteins that typically function by repressing transcription. Here, we present evidence that MvaT controls phase-variable (ON/OFF) expression of the cupA fimbrial gene cluster. Using a directed proteomic approach, we show that MvaT associates with a related protein in P. aeruginosa called MvaU. Analysis with a bacterial two-hybrid system designed to facilitate the study of protein dimerization indicates that MvaT and MvaU can form both heteromeric and homomeric complexes, and that formation of these complexes is mediated through the N-terminal regions of MvaT and MvaU, both of which are predicted to adopt a coiled-coil conformation. We show further that, like MvaT, MvaU can repress phase-variable expression of the cupA gene cluster. Our findings suggest that fimbrial genes important for biofilm formation can be expressed in a phase-variable manner in P. aeruginosa, provide insight into the molecular mechanism of MvaT-dependent gene control, and lend further weight to the postulate that MvaT proteins are H-NS-like in nature.
铜绿假单胞菌的cupA基因簇编码一种假定的菌毛结构成分,使这种机会性人类病原体能够在非生物表面形成生物膜。在铜绿假单胞菌中,cupA基因表达受MvaT抑制,MvaT是一种假定的转录调节因子,被认为属于类核相关蛋白的H-NS家族,通常通过抑制转录发挥作用。在此,我们提供证据表明MvaT控制cupA菌毛基因簇的相变(开/关)表达。使用定向蛋白质组学方法,我们表明MvaT与铜绿假单胞菌中一种名为MvaU的相关蛋白相互作用。用旨在促进蛋白质二聚化研究的细菌双杂交系统分析表明,MvaT和MvaU可以形成异源和同源复合物,并且这些复合物的形成是通过MvaT和MvaU的N端区域介导的,这两个区域预计会形成卷曲螺旋构象。我们进一步表明,与MvaT一样,MvaU也可以抑制cupA基因簇的相变表达。我们的研究结果表明,对生物膜形成重要的菌毛基因在铜绿假单胞菌中可以以相变方式表达,深入了解了MvaT依赖性基因控制的分子机制,并进一步支持了MvaT蛋白本质上类似H-NS的假设。