TMPRSS6
海西定
汉普
丝氨酸蛋白酶
缺铁性贫血
突变体
丝氨酸
生物
血色病
缺铁
细胞生物学
化学
生物化学
基因
蛋白酶
贫血
遗传学
磷酸化
内科学
酶
免疫学
医学
炎症
作者
Xin Du,Ellen She,Terri Gelbart,Jaroslav Truksa,Pauline Lee,Yu Xia,Kevin Khovananth,Suzanne Mudd,Navjiwan Mann,Eva Marie Y. Moresco,Ernest Beutler,Bruce Beutler
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2008-05-04
卷期号:320 (5879): 1088-1092
被引量:580
标识
DOI:10.1126/science.1157121
摘要
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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