Mammalian iron metabolism and its control by iron regulatory proteins

被引:390
作者
Anderson, Cole P. [1 ]
Shen, Macy [2 ]
Eisenstein, Richard S. [2 ]
Leibold, Elizabeth A. [1 ,3 ]
机构
[1] Univ Utah, Dept Oncol Sci, Salt Lake City, UT 84112 USA
[2] Univ Wisconsin, Dept Nutr Sci, Madison, WI 53706 USA
[3] Univ Utah, Dept Med, Salt Lake City, UT 84112 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2012年 / 1823卷 / 09期
关键词
Iron; IRP; Iron-responsive element; RNA-binding protein; Iron-sulfur protein; Post-transcriptional regulation; FERRITIN MESSENGER-RNA; AMYLOID PRECURSOR PROTEIN; ELEMENT-BINDING-PROTEIN; HYPOXIA-INDUCIBLE FACTOR-2-ALPHA; SULFUR CLUSTER BIOGENESIS; HEMERYTHRIN-LIKE DOMAIN; RESPONSIVE ELEMENT; TRANSLATIONAL REGULATION; MITOCHONDRIAL ACONITASE; DEPENDENT DEGRADATION;
D O I
10.1016/j.bbamcr.2012.05.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular iron homeostasis is maintained by iron regulatory proteins 1 and 2 (IRP1 and IRP2). IRPs bind to iron-responsive elements (IREs) located in the untranslated regions of mRNAs encoding protein involved in iron uptake, storage, utilization and export. Over the past decade, significant progress has been made in understanding how IRPs are regulated by iron-dependent and iron-independent mechanisms and the pathological consequences of IRP2 deficiency in mice. The identification of novel IREs involved in diverse cellular pathways has revealed that the IRP-IRE network extends to processes other than iron homeostasis. A mechanistic understanding of IRP regulation will likely yield important insights into the basis of disorders of iron metabolism. This article is part of a Special Issue entitled: Cell Biology of Metals. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1468 / 1483
页数:16
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