Hereditary hemochromatosis protein, HFE, interaction with transferrin receptor 2 suggests a molecular mechanism for mammalian iron sensing

被引:258
作者
Goswami, Tapasree
Andrews, Nancy C.
机构
[1] Harvard Univ, Sch Med, Childrens Hosp Boston, Karp Family Res Labs,Div Hematol Oncol, Boston, MA 02115 USA
[2] Howard Hughes Med Inst, Boston, MA 02115 USA
关键词
D O I
10.1074/jbc.C600197200
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
HFE and transferrin receptor 2 (TFR2) are membrane proteins integral to mammalian iron homeostasis and associated with human hereditary hemochromatosis. Here we demonstrate that HFE and TFR2 interact in cells, that this interaction is not abrogated by disease-associated mutations of HFE and TFR2, and that TFR2 competes with TFR1 for binding to HFE. We propose a new model for the mechanism of iron status sensing that results in the regulation of iron homeostasis.
引用
收藏
页码:28494 / 28498
页数:5
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