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

Author:

Butcher Bronwyn G.1,Bronstein Philip A.12,Myers Christopher R.3,Stodghill Paul V.2,Bolton James J.2,Markel Eric J.2,Filiatrault Melanie J.12,Swingle Bryan12,Gaballa Ahmed4,Helmann John D.4,Schneider David J.12,Cartinhour Samuel W.12

Affiliation:

1. Department of Plant Pathology and Plant-Microbe Biology, Cornell University, Ithaca, New York 14853

2. United States Department of Agriculture-Agricultural Research Service, Ithaca, New York 14853

3. Department of Physics, Laboratory of Atomic and Solid State Physics, and Computational Biology Service Unit, Cornell University, Ithaca, New York 14853

4. Department of Microbiology, Cornell University, Ithaca, New York 14853

Abstract

ABSTRACT 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).

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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