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

被引:259
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
相关论文
共 20 条
[1]  
Ausubel F.M., CURRENT PROTOCOLS MO
[2]   Crystal structure of the hereditary haemochromatosis protein HFE complexed with transferrin receptor [J].
Bennett, MJ ;
Lebrón, JA ;
Bjorkman, PJ .
NATURE, 2000, 403 (6765) :46-53
[3]   Co-localization of the mammalian hemochromatosis gene product (HFE) and a newly identified transferrin receptor (TfR2) in intestinal tissue and cells [J].
Griffiths, WJH ;
Cox, TM .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2003, 51 (05) :613-623
[4]   Balancing acts: Molecular control of mammalian iron metabolism [J].
Hentze, MW ;
Muckenthaler, MU ;
Andrews, NC .
CELL, 2004, 117 (03) :285-297
[5]   REGULATION OF FERRITIN AND TRANSFERRIN RECEPTOR EXPRESSION BY IRON IN HUMAN HEPATOCYTE CULTURES [J].
HUBERT, N ;
LESCOAT, G ;
SCIOT, R ;
MOIRAND, R ;
JEGO, P ;
LEROYER, P ;
BRISSOT, P .
JOURNAL OF HEPATOLOGY, 1993, 18 (03) :301-312
[6]   Diferric transferrin regulates transferrin receptor 2 protein stability [J].
Johnson, MB ;
Enns, CA .
BLOOD, 2004, 104 (13) :4287-4293
[7]   Molecular cloning of transferrin receptor 2 - A new member of the transferrin receptor-like family [J].
Kawabata, H ;
Yang, S ;
Hirama, T ;
Vuong, PT ;
Kawano, S ;
Gombart, AF ;
Koeffler, HP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (30) :20826-20832
[8]   The molecular genetics of haemochromatosis [J].
Le Gac, G ;
Férec, C .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (11) :1172-1185
[9]   The C282Y mutation causing hereditary hemochromatosis does not produce a null allele [J].
Levy, JE ;
Montross, LK ;
Cohen, DE ;
Fleming, MD ;
Andrews, NC .
BLOOD, 1999, 94 (01) :9-11
[10]   FUNCTIONAL EXPRESSION OF THE HUMAN TRANSFERRIN RECEPTOR CDNA IN CHINESE-HAMSTER OVARY CELLS DEFICIENT IN ENDOGENOUS TRANSFERRIN RECEPTOR [J].
MCGRAW, TE ;
GREENFIELD, L ;
MAXFIELD, FR .
JOURNAL OF CELL BIOLOGY, 1987, 105 (01) :207-214