The Pseudomonas aeruginosaAmrZ C-terminal domain mediates tetramerization and is required for its activator and repressor functions

被引:12
|
作者
Xu, Binjie [1 ,4 ]
Ju, Yue [2 ]
Soukup, Randal J. [5 ]
Ramsey, Deborah M. [8 ,9 ]
Fishel, Richard [6 ,7 ]
Wysocki, Vicki H. [2 ]
Wozniak, Daniel J. [1 ,3 ,4 ]
机构
[1] Ohio State Univ, Wexner Med Ctr, Dept Microbiol, Columbus, OH 43210 USA
[2] Ohio State Univ, Wexner Med Ctr, Dept Chem & Biochem, Columbus, OH 43210 USA
[3] Ohio State Univ, Wexner Med Ctr, Dept Microbial Infect & Immun, Columbus, OH 43210 USA
[4] Ohio State Univ, Wexner Med Ctr, Ctr Microbial Interface Biol, Columbus, OH 43210 USA
[5] Ohio State Univ, Wexner Med Ctr, Mol Cellular & Dev Biol Grad Program, Columbus, OH 43210 USA
[6] Ohio State Univ, Wexner Med Ctr, Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[7] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[8] Wake Forest Sch Med, Dept Microbiol & Immunol, Winston Salem, NC 27157 USA
[9] ConversantBio, 601 Genome Way,Suite 1200, Huntsville, AL 35806 USA
来源
ENVIRONMENTAL MICROBIOLOGY REPORTS | 2016年 / 8卷 / 01期
关键词
DNA-BINDING PROTEIN; ALGINATE SYNTHESIS; MNT REPRESSORS; AMRZ; ALGZ; ARC; TRANSCRIPTION; BIOSYNTHESIS; SEQUENCE;
D O I
10.1111/1758-2229.12354
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Pseudomonas aeruginosa is an important bacterial opportunistic pathogen, presenting a significant threat towards individuals with underlying diseases such as cystic fibrosis. The transcription factor AmrZ regulates expression of multiple P.aeruginosa virulence factors. AmrZ belongs to the ribbon-helix-helix protein superfamily, in which many members function as dimers, yet others form higher order oligomers. In this study, four independent approaches were undertaken and demonstrated that the primary AmrZ form in solution is tetrameric. Deletion of the AmrZ C-terminal domain leads to loss of tetramerization and reduced DNA binding to both activated and repressed target promoters. Additionally, the C-terminal domain is essential for efficient AmrZ-mediated activation and repression of its targets.
引用
收藏
页码:85 / 90
页数:6
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