دورية أكاديمية

An Oxygen-Dependent Interaction between FBXL5 and the CIA-Targeting Complex Regulates Iron Homeostasis.

التفاصيل البيبلوغرافية
العنوان: An Oxygen-Dependent Interaction between FBXL5 and the CIA-Targeting Complex Regulates Iron Homeostasis.
المؤلفون: Mayank AK; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Pandey V; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Vashisht AA; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Barshop WD; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Rayatpisheh S; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Sharma T; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Haque T; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Powers DN; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA., Wohlschlegel JA; Department of Biological Chemistry, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA. Electronic address: jwohl@ucla.edu.
المصدر: Molecular cell [Mol Cell] 2019 Jul 25; Vol. 75 (2), pp. 382-393.e5. Date of Electronic Publication: 2019 Jun 19.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural
اللغة: English
بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 9802571 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-4164 (Electronic) Linking ISSN: 10972765 NLM ISO Abbreviation: Mol Cell Subsets: MEDLINE
أسماء مطبوعة: Publication: Cambridge Ma : Cell Press
Original Publication: Cambridge, Mass. : Cell Press, c1997-
مواضيع طبية MeSH: Cell Cycle Proteins/*genetics , F-Box Proteins/*genetics , Molecular Chaperones/*genetics , Multiprotein Complexes/*genetics , Ubiquitin-Protein Ligase Complexes/*genetics, Cell Cycle Proteins/chemistry ; F-Box Proteins/chemistry ; HeLa Cells ; Homeostasis ; Humans ; Iron/metabolism ; Iron-Regulatory Proteins/genetics ; Iron-Sulfur Proteins/chemistry ; Iron-Sulfur Proteins/genetics ; Molecular Chaperones/chemistry ; Multiprotein Complexes/chemistry ; Oxygen/metabolism ; Proteolysis ; Transcription Factors/genetics ; Ubiquitin-Protein Ligase Complexes/chemistry
مستخلص: The iron-sensing protein FBXL5 is the substrate adaptor for a SKP1-CUL1-RBX1 E3 ubiquitin ligase complex that regulates the degradation of iron regulatory proteins (IRPs). Here, we describe a mechanism of FBXL5 regulation involving its interaction with the cytosolic Fe-S cluster assembly (CIA) targeting complex composed of MMS19, FAM96B, and CIAO1. We demonstrate that the CIA-targeting complex promotes the ability of FBXL5 to degrade IRPs. In addition, the FBXL5-CIA-targeting complex interaction is regulated by oxygen (O 2 ) tension displaying a robust association in 21% O 2 that is severely diminished in 1% O 2 and contributes to O 2 -dependent regulation of IRP degradation. Together, these data identify a novel oxygen-dependent signaling axis that links IRP-dependent iron homeostasis with the Fe-S cluster assembly machinery.
(Copyright © 2019 Elsevier Inc. All rights reserved.)
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معلومات مُعتمدة: R01 GM089778 United States GM NIGMS NIH HHS; R01 GM112763 United States GM NIGMS NIH HHS; T32 GM007185 United States GM NIGMS NIH HHS
فهرسة مساهمة: Keywords: CIA-targeting complex; CIAO1; FAM96B; FBXL5; IRP1; IRP2; MMS19; hypoxia; iron homeostasis; iron metabolism
المشرفين على المادة: 0 (ASF1A protein, human)
0 (Cell Cycle Proteins)
0 (F-Box Proteins)
0 (FBXL5 protein, human)
0 (Iron-Regulatory Proteins)
0 (Iron-Sulfur Proteins)
0 (Molecular Chaperones)
0 (Multiprotein Complexes)
0 (Transcription Factors)
E1UOL152H7 (Iron)
EC 2.3.2.23 (Ubiquitin-Protein Ligase Complexes)
S88TT14065 (Oxygen)
تواريخ الأحداث: Date Created: 20190624 Date Completed: 20200124 Latest Revision: 20200725
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC6660392
DOI: 10.1016/j.molcel.2019.05.020
PMID: 31229404
قاعدة البيانات: MEDLINE
الوصف
تدمد:1097-4164
DOI:10.1016/j.molcel.2019.05.020