The Serine Protease TMPRSS6 Is Required to Sense Iron Deficiency
2008
Du, Xin | She, Ellen | Gelbart, Terri | Truksa, Jaroslav | Lee, Pauline | Xia, Yu | Khovananth, Kevin | Mudd, Suzanne | Mann, Navjiwan | Moresco, Eva Marie Y. | Beutler, Ernest | Beutler, Bruce
Hepcidin, a liver-derived protein that restricts enteric iron absorption, is the key regulator of body iron content. Several proteins induce expression of the hepcidin-encoding gene Hamp in response to infection or high levels of iron. However, mechanism(s) of Hamp suppression during iron depletion are poorly understood. We describe mask: a recessive, chemically induced mutant mouse phenotype, characterized by progressive loss of body (but not facial) hair and microcytic anemia. The mask phenotype results from reduced absorption of dietary iron caused by high levels of hepcidin and is due to a splicing defect in the transmembrane serine protease 6 gene Tmprss6. Overexpression of normal TMPRSS6 protein suppresses activation of the Hamp promoter, and the TMPRSS6 cytoplasmic domain mediates Hamp suppression via proximal promoter element(s). TMPRSS6 is an essential component of a pathway that detects iron deficiency and blocks Hamp transcription, permitting enhanced dietary iron absorption.
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