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Escherichia coli str. K-12 substr. MG1655

ABSTRACT: Deciphering the Fur transcriptional regulatory network highlights its complex role beyond iron metabolism in Escherichia coli [ChIP-Seq]

PROVIDER: PRJNA238004 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR1168130.fastq.gz	Fastqsanger.gz
	SRR1168121.fastq.gz	Fastqsanger.gz
	SRR1168131.fastq.gz	Fastqsanger.gz
	SRR1168122.fastq.gz	Fastqsanger.gz
	SRR1168132.fastq.gz	Fastqsanger.gz

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Escherichia coli str. K-12 substr. MG1655

Project description:Deciphering the Fur transcriptional regulatory network highlights its complex role beyond iron metabolism in Escherichia coli [RNA-seq]

| PRJNA238005 | ENA

Deciphering the Fur transcriptional regulatory network highlights its complex role beyond iron metabolism in Escherichia coli

Project description:Deciphering the Fur transcriptional regulatory network highlights its complex role beyond iron metabolism in Escherichia coli

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Deciphering the Fur transcriptional regulatory network highlights its complex role beyond iron metabolism in Escherichia coli [RNA-seq]

Project description:The ferric uptake regulator (Fur) plays a critical role in the transcriptional regulation of iron metabolism in many bacteria. However, the full regulatory potential of Fur beyond iron metabolism remains undefined. Here, we comprehensively reconstructed the Fur transcriptional regulatory network in Escherichia coli K-12 MG1655 in response to iron availability using genome-wide measurements (ChIP-exo and RNA-seq). Polyomic data analysis revealed that a total of 81 genes in 42 transcription units (TUs) are directly regulated by three different modes of Fur regulation, including apo- and holo-Fur activation as well as holo-Fur repression. We showed that Fur connects iron transport and utilization enzymes with negative-feedback loop pairs for iron homeostasis. In addition, direct involvement of Fur in the regulation of DNA synthesis, energy metabolism, and biofilm development was found. These results indicate that Fur exhibits a comprehensive regulatory role affecting many fundamental cellular processes linked to iron metabolism in order to coordinate E. coli responses to the availability of iron. [RNA-seq]: A total of eight samples were analyzed. WT and fur mutant cells were cultured in the presense and absence of iron with biological duplicates. DPD = iron chelator.

2014-09-09 | E-GEOD-54900 | biostudies-arrayexpress

Deciphering the Fur transcriptional regulatory network highlights its complex role beyond iron metabolism in Escherichia coli [RNA-seq]

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Deciphering the Fur transcriptional regulatory network highlights its complex role beyond iron metabolism in Escherichia coli [ChIP-Seq]

2014-09-09 | GSE54899 | GEO

Deciphering the Fur transcriptional regulatory network highlights its complex role beyond iron metabolism in Escherichia coli [ChIP-Seq]

Project description:The ferric uptake regulator (Fur) plays a critical role in the transcriptional regulation of iron metabolism in many bacteria. However, the full regulatory potential of Fur beyond iron metabolism remains undefined. Here, we comprehensively reconstructed the Fur transcriptional regulatory network in Escherichia coli K-12 MG1655 in response to iron availability using genome-wide measurements (ChIP-exo and RNA-seq). Polyomic data analysis revealed that a total of 81 genes in 42 transcription units (TUs) are directly regulated by three different modes of Fur regulation, including apo- and holo-Fur activation as well as holo-Fur repression. We showed that Fur connects iron transport and utilization enzymes with negative-feedback loop pairs for iron homeostasis. In addition, direct involvement of Fur in the regulation of DNA synthesis, energy metabolism, and biofilm development was found. These results indicate that Fur exhibits a comprehensive regulatory role affecting many fundamental cellular processes linked to iron metabolism in order to coordinate E. coli responses to the availability of iron. [ChIP-exo]: A total of twelve samples were analyzed. WT and Fur-8-myc tagged cells were cultured in the presense and absence of iron with biological duplicates. To analyze static RNAP binding, rifampicin was also added to the media with biological duplicates. DPD = iron chelator.

2014-09-09 | E-GEOD-54899 | biostudies-arrayexpress

Proteomic studies of Escherichia coli CFT073 and MG1655

Project description:Here we dissected a regulatory network directed by the conserved iron homeostasis regulator, Ferric Uptake Regulator (Fur), in uropathogenic E. coli strain CFT073. Comparing anaerobic genome-scale Fur DNA binding, with Fur dependent transcript expression and protein levels of the uropathogen to that of commensal E. coli K-12 strain MG1655, showed that the Fur regulon of the core genome is conserved but also includes genes within the pathogenicity/genetic islands. Unexpectedly, regulons indicative of amino acid limitation and the general stress response were also indirectly activated in the uropathogen fur mutant, suggesting that induction of the Fur regulon increases amino acid demand. Using RpoS levels as a proxy, addition of amino acids mitigated the stress. In addition, iron chelation increased RpoS to the same levels as in the fur mutant. The increased amino acid demand of the fur mutant or iron chelated cells was exacerbated by aerobic conditions, which could be partly explained by the O 2 -dependent synthesis of the siderophore aerobactin, encoded within a pathogenicity island. Taken together, this data suggest in the iron-poor environment of the urinary tract, amino acid availability could play a role in the proliferation of this uropathogen, particularly if there is sufficient O 2 to produce aerobactin.

2020-05-27 | PXD017582 | Pride

Escherichia coli str. K-12 substr. MG1655

Project description:The impact of anaerobiosis on expression of the iron-responsive Fur and RyhB Regulons [expression microarray]

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Escherichia coli str. K-12 substr. MG1655

Project description:The impact of anaerobiosis on expression of the iron-responsive Fur and RyhB Regulons [ChIP-seq]

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Escherichia coli str. K-12 substr. MG1655

Project description:The impact of anaerobiosis on expression of the iron-responsive Fur and RyhB Regulons [ChIP-chip]

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