Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes.

Escherichia coli FadR plays two regulatory roles in fatty acid metabolism. FadR represses the fatty acid degradation (fad) system and activates the unsaturated fatty acid synthetic pathway. Cross-talk between E. coli FadR and the ArcA-ArcB oxygen-responsive two-component system was observed that res...

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Main Authors: Youjun Feng, John E Cronan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3460868?pdf=render
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spelling doaj-d4459784ec504f39b55f97fd599a3ac82020-11-25T01:28:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4627510.1371/journal.pone.0046275Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes.Youjun FengJohn E CronanEscherichia coli FadR plays two regulatory roles in fatty acid metabolism. FadR represses the fatty acid degradation (fad) system and activates the unsaturated fatty acid synthetic pathway. Cross-talk between E. coli FadR and the ArcA-ArcB oxygen-responsive two-component system was observed that resulted in diverse regulation of certain fad regulon β-oxidation genes. We have extended such analyses to the fadL and fadD genes, the protein products of which are required for long chain fatty acid transport and have also studied the role of a third global regulator, the CRP-cAMP complex. The promoters of both the fadL and fadD genes contain two experimentally validated FadR-binding sites plus binding sites for ArcA and CRP-cAMP. Despite the presence of dual binding sites FadR only modestly regulates expression of these genes, indicating that the number of binding sites does not determine regulatory strength. We report complementary in vitro and in vivo studies indicating that the CRP-cAMP complex directly activates expression of fadL and fadD as well as the β-oxidation gene, fadH. The physiological relevance of the fadL and fadD transcription data was validated by direct assays of long chain fatty acid transport.http://europepmc.org/articles/PMC3460868?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Youjun Feng
John E Cronan
spellingShingle Youjun Feng
John E Cronan
Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes.
PLoS ONE
author_facet Youjun Feng
John E Cronan
author_sort Youjun Feng
title Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes.
title_short Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes.
title_full Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes.
title_fullStr Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes.
title_full_unstemmed Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes.
title_sort crosstalk of escherichia coli fadr with global regulators in expression of fatty acid transport genes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Escherichia coli FadR plays two regulatory roles in fatty acid metabolism. FadR represses the fatty acid degradation (fad) system and activates the unsaturated fatty acid synthetic pathway. Cross-talk between E. coli FadR and the ArcA-ArcB oxygen-responsive two-component system was observed that resulted in diverse regulation of certain fad regulon β-oxidation genes. We have extended such analyses to the fadL and fadD genes, the protein products of which are required for long chain fatty acid transport and have also studied the role of a third global regulator, the CRP-cAMP complex. The promoters of both the fadL and fadD genes contain two experimentally validated FadR-binding sites plus binding sites for ArcA and CRP-cAMP. Despite the presence of dual binding sites FadR only modestly regulates expression of these genes, indicating that the number of binding sites does not determine regulatory strength. We report complementary in vitro and in vivo studies indicating that the CRP-cAMP complex directly activates expression of fadL and fadD as well as the β-oxidation gene, fadH. The physiological relevance of the fadL and fadD transcription data was validated by direct assays of long chain fatty acid transport.
url http://europepmc.org/articles/PMC3460868?pdf=render
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AT johnecronan crosstalkofescherichiacolifadrwithglobalregulatorsinexpressionoffattyacidtransportgenes
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