Characterization of the Fur Regulon in Pseudomonas syringae pv. tomato DC3000

被引:44
|
作者
Butcher, Bronwyn G.
Bronstein, Philip A.
Myers, Christopher R. [2 ,3 ]
Stodghill, Paul V.
Bolton, James J.
Markel, Eric J.
Filiatrault, Melanie J.
Swingle, Bryan
Gaballa, Ahmed [4 ]
Helmann, John D. [4 ]
Schneider, David J.
Cartinhour, Samuel W. [1 ]
机构
[1] Cornell Univ, USDA ARS, Plant Microbe Interact Res Unit, Dept Plant Pathol & Plant Microbe Biol, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Phys, Atom & Solid State Phys Lab, Ithaca, NY 14853 USA
[3] Cornell Univ, Computat Biol Serv Unit, Ithaca, NY 14853 USA
[4] Cornell Univ, Dept Microbiol, Ithaca, NY 14853 USA
关键词
FERRIC UPTAKE REGULATOR; ESCHERICHIA-COLI; HELICOBACTER-PYLORI; TRANSCRIPTOME ANALYSIS; IRON HOMEOSTASIS; GENE-EXPRESSION; SMALL RNAS; H-NS; AERUGINOSA; REPRESSOR;
D O I
10.1128/JB.00340-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The plant pathogen Pseudomonas syringae pv. tomato DC3000 (DC3000) is found in a wide variety of environments and must monitor and respond to various environmental signals such as the availability of iron, an essential element for bacterial growth. An important regulator of iron homeostasis is Fur (ferric uptake regulator), and here we present the first study of the Fur regulon in DC3000. Using chromatin immunoprecipitation followed by massively parallel sequencing (ChIP-seq), 312 chromosomal regions were highly enriched by coimmunoprecipitation with a C-terminally tagged Fur protein. Integration of these data with previous microarray and global transcriptome analyses allowed us to expand the putative DC3000 Fur regulon to include genes both repressed and activated in the presence of bioavailable iron. Using nonradioactive DNase I footprinting, we confirmed Fur binding in 41 regions, including upstream of 11 iron-repressed genes and the iron-activated genes encoding two bacterioferritins (PSPTO_0653 and PSPTO_4160), a ParA protein (PSPTO_0855), and a two-component system (TCS) (PSPTO_3382 to PSPTO_3380).
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页码:4598 / 4611
页数:14
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