Fe-S cluster containing proteins are ubiquitous and participate in diverse and essential cellular functions. The destruction of Fe-S clusters that occurs as a consequence of aerobic metabolism places a burden on cells (termed Fe-S stress) to replace essential proteins and deal with the resulting oxidative damage. Oxidative damage is an underlying cause of chronic and late onset diseases and therefore, it is important to decipher cellular responses to Fe-S stress. A long-term goal is to identify the pathways by which cells respond to Fe-S stress and avoid the potentially lethal oxidative damage caused by cluster destruction or loss of essential functions. This research plan studies Fe-S stress in the bacterium E. coli because there is a wealth of knowledge about the pathways of Fe-S cluster synthesis and the mechanisms of reactive oxygen species (ROS)-mediated Fe-S protein damage. The proposed studies will reveal the components of a Fe-S stress response that is directed by the Fe-S transcription factor, IscR in E. coli. The biochemical and cellular properties of [2Fe-2S]-IscR will be investigated to determine the role of oxygen and ROS in sensing Fe-S stress. These studies will test the model that Fe-S stress alters the function of IscR by changing the occupancy of the Fe-S cluster, thereby switching the suites of target genes in response to Fe-S occupancy of IscR. The DNA binding properties of IscR and the different classes of DNA sites recognized by this protein in the presence or absence of the Fe-S will be studied to understand how target genes recognition is regulated by Fe-S occupancy. The role of target genes in attenuating Fe-S stress will be investigated using genetic and molecular approaches. These studies will define how Fe-S proteins function as sensors of O2 or ROS and how they control transcription of target genes in response to Fe-S stress. The fundamental insights that we gain from the proposed studies will advance our understanding of Fe-S homeostatic mechanisms and the response to toxic ROS across biological systems.
Inadvertent reactions of iron and oxygen damage cellular components and over the long term lead to disease. We are studying the pathways that maintain a class of iron proteins at their appropriate levels for cell function and the mechanisms that attenuate cell damage when the pathways go awry.
|Beauchene, Nicole A; Mettert, Erin L; Moore, Laura J et al. (2017) O2 availability impacts iron homeostasis in Escherichia coli. Proc Natl Acad Sci U S A 114:12261-12266|
|Myers, Kevin S; Park, Dan M; Beauchene, Nicole A et al. (2015) Defining bacterial regulons using ChIP-seq. Methods 86:80-8|
|Beauchene, Nicole A; Myers, Kevin S; Chung, Dongjun et al. (2015) Impact of Anaerobiosis on Expression of the Iron-Responsive Fur and RyhB Regulons. MBio 6:e01947-15|
|Mettert, Erin L; Kiley, Patricia J (2015) Fe-S proteins that regulate gene expression. Biochim Biophys Acta 1853:1284-93|
|Tolla, Dean A; Kiley, Patricia J; Lomnitz, Jason G et al. (2015) Design principles of a conditional futile cycle exploited for regulation. Mol Biosyst 11:1841-9|
|Miller, Halie K; Kwuan, Laura; Schwiesow, Leah et al. (2014) IscR is essential for yersinia pseudotuberculosis type III secretion and virulence. PLoS Pathog 10:e1004194|
|Park, Dan M; Kiley, Patricia J (2014) The influence of repressor DNA binding site architecture on transcriptional control. MBio 5:e01684-14|
|Mettert, Erin L; Kiley, Patricia J (2014) Coordinate regulation of the Suf and Isc Fe-S cluster biogenesis pathways by IscR is essential for viability of Escherichia coli. J Bacteriol 196:4315-23|
|Chung, Dongjun; Park, Dan; Myers, Kevin et al. (2013) dPeak: high resolution identification of transcription factor binding sites from PET and SET ChIP-Seq data. PLoS Comput Biol 9:e1003246|
|Myers, Kevin S; Yan, Huihuang; Ong, Irene M et al. (2013) Genome-scale analysis of escherichia coli FNR reveals complex features of transcription factor binding. PLoS Genet 9:e1003565|
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