2Department of Dermatology, Columbia University, College of Physicians and Surgeons, Russ Berrie Medical Science Pavilion, 1150 St. Nicholas Ave., Rm. 307, New York, NY 10032, USA.
FASEB J. 2014 Apr;28(4):1534-42. doi: 10.1096/fj.13-237677. Epub 2013 Dec 13.
The hairless (HR) protein contains a Jumonji C (JmjC) domain that is conserved among a family of proteins with histone demethylase (HDM) activity. To test whether HR possesses HDM activity, we performed a series of in vitro demethylation assays, which demonstrated that HR can demethylate monomethylated or dimethylated histone H3 lysine 9 (H3K9me1 or me2). Moreover, ectopic expression of wild-type HR, but not JmjC-mutant HR, led to pronounced demethylation of H3K9 in cultured human HeLa cells. We also show that two missense mutations in HR, which we and others described in patients with atrichia with papular lesions, abolished the demethylase activity of HR, demonstrating the role of HR demethylase activity in human disease. By ChIP-Seq analysis, we identified multiple new HR target genes, many of which play important roles in epidermal development, neural function, and transcriptional regulation, consistent with the predicted biological functions of HR. Our findings demonstrate for the first time that HR is a H3K9 demethylase that regulates epidermal homeostasis via direct control of its target genes.
无毛(HR)蛋白含有一个 Jumonji C(JmjC)结构域,该结构域在具有组蛋白去甲基酶(HDM)活性的蛋白质家族中保守。为了测试 HR 是否具有 HDM 活性,我们进行了一系列体外去甲基化测定,结果表明 HR 可以去甲基化单甲基化或二甲基化组蛋白 H3 赖氨酸 9(H3K9me1 或 me2)。此外,野生型 HR 的异位表达,但不是 JmjC 突变型 HR 的异位表达,导致培养的人 HeLa 细胞中 H3K9 的明显去甲基化。我们还表明,我们和其他人在具有丘疹病变的无毛症患者中描述的 HR 中的两个错义突变,消除了 HR 的去甲基酶活性,证明了 HR 去甲基酶活性在人类疾病中的作用。通过 ChIP-Seq 分析,我们鉴定了多个新的 HR 靶基因,其中许多在表皮发育、神经功能和转录调节中发挥重要作用,与 HR 的预测生物学功能一致。我们的发现首次证明 HR 是一种 H3K9 去甲基酶,通过直接控制其靶基因来调节表皮内稳态。