| Literature DB >> 31229404 |
Adarsh K Mayank1, Vijaya Pandey1, Ajay A Vashisht1, William D Barshop1, Shima Rayatpisheh1, Tanu Sharma1, Tisha Haque1, David N Powers1, James A Wohlschlegel2.
Abstract
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 (O2) tension displaying a robust association in 21% O2 that is severely diminished in 1% O2 and contributes to O2-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.Entities:
Keywords: CIA-targeting complex; CIAO1; FAM96B; FBXL5; IRP1; IRP2; MMS19; hypoxia; iron homeostasis; iron metabolism
Mesh:
Substances:
Year: 2019 PMID: 31229404 PMCID: PMC6660392 DOI: 10.1016/j.molcel.2019.05.020
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970