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ReportsControl of Iron Homeostasis by an Iron-Regulated Ubiquitin Ligase
Eukaryotic cells require iron for survival and have developed regulatory mechanisms for maintaining appropriate intracellular iron concentrations. The degradation of iron regulatory protein 2 (IRP2) in iron-replete cells is a key event in this pathway, but the E3 ubiquitin ligase responsible for its proteolysis has remained elusive. We found that a SKP1-CUL1-FBXL5 ubiquitin ligase protein complex associates with and promotes the iron-dependent ubiquitination and degradation of IRP2. The F-box substrate adaptor protein FBXL5 was degraded upon iron and oxygen depletion in a process that required an iron-binding hemerythrin-like domain in its N terminus. Thus, iron homeostasis is regulated by a proteolytic pathway that couples IRP2 degradation to intracellular iron levels through the stability and activity of FBXL5.
1 Department of Biological Chemistry, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
2 Departments of Medicine and Oncological Sciences, University of Utah, Salt Lake City, UT 84112, USA. 3 Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, USA. 4 Sidney Kimmel Cancer Center, San Diego, CA 92121, USA. 5 Cancer Center Karolinska, Department of Oncology and Pathology, Karolinska Hospital, SE-171 76 Stockholm, Sweden. 6 School of Biotechnology, Department of Proteomics, Royal Institute of Technology/AlbaNova, SE-106 91 Stockholm, Sweden. * To whom correspondence should be addressed. E-mail: jwohl{at}mednet.ucla.edu
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Science. ISSN 0036-8075 (print), 1095-9203 (online)