Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.16/2232
Title: Hepcidin is regulated by promoter-associated histone acetylation and HDAC3
Author: Pasricha, S.
Lim, P.
Duarte, T.
Casu, C.
Oosterhuis, D.
Mleczko-Sanecka, K.
Suciu, M.
Da Silva, A.
Al-Hourani, K.
Arezes, J.
McHugh, K.
Gooding, S.
Frost, J.
Wray, K.
Santos, A.
Porto, G.
Repapi, E.
Gray, N.
Draper, S.
Ashley, N.
Soilleux, E.
Olinga, P.
Muckenthaler, M.
Hughes, J.
Rivella, S.
Milne, T.
Armitage, A.
Drakesmith, H.
Issue Date: 1-Sep-2017
Publisher: Nature Publishing Group
Citation: Nat Commun. 2017 Sep 1;8(1):403
Abstract: Hepcidin regulates systemic iron homeostasis. Suppression of hepcidin expression occurs physiologically in iron deficiency and increased erythropoiesis but is pathologic in thalassemia and hemochromatosis. Here we show that epigenetic events govern hepcidin expression. Erythropoiesis and iron deficiency suppress hepcidin via erythroferrone-dependent and -independent mechanisms, respectively, in vivo, but both involve reversible loss of H3K9ac and H3K4me3 at the hepcidin locus. In vitro, pan-histone deacetylase inhibition elevates hepcidin expression, and in vivo maintains H3K9ac at hepcidin-associated chromatin and abrogates hepcidin suppression by erythropoietin, iron deficiency, thalassemia, and hemochromatosis. Histone deacetylase 3 and its cofactor NCOR1 regulate hepcidin; histone deacetylase 3 binds chromatin at the hepcidin locus, and histone deacetylase 3 knockdown counteracts hepcidin suppression induced either by erythroferrone or by inhibiting bone morphogenetic protein signaling. In iron deficient mice, the histone deacetylase 3 inhibitor RGFP966 increases hepcidin, and RNA sequencing confirms hepcidin is one of the genes most differentially regulated by this drug in vivo. We conclude that suppression of hepcidin expression involves epigenetic regulation by histone deacetylase 3.Hepcidin controls systemic iron levels by inhibiting intestinal iron absorption and iron recycling. Here, Pasricha et al. demonstrate that the hepcidin-chromatin locus displays HDAC3-mediated reversible epigenetic modifications during both erythropoiesis and iron deficiency.
Peer review: yes
URI: http://hdl.handle.net/10400.16/2232
DOI: 10.1038/s41467-017-00500-z
ISSN: 2041-1723
Publisher Version: https://www.nature.com/articles/s41467-017-00500-z.pdf
Appears in Collections:SHC - Artigos publicados em revistas indexadas na Medline

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