Histone H4K20/H3K9 demethylase PHF8 regulates zebrafish brain and craniofacial development

被引:0
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作者
Hank H. Qi
Madathia Sarkissian
Gang-Qing Hu
Zhibin Wang
Arindam Bhattacharjee
D. Benjamin Gordon
Michelle Gonzales
Fei Lan
Pat P. Ongusaha
Maite Huarte
Nasser K. Yaghi
Huijun Lim
Benjamin A. Garcia
Leonardo Brizuela
Keji Zhao
Thomas M. Roberts
Yang Shi
机构
[1] Harvard Medical School,Department of Pathology
[2] Children’s Hospital,Division of Newborn Medicine, Department of Medicine
[3] Dana Farber Cancer Institute,Department of Cancer Biology
[4] Laboratory of Molecular Immunology,Department of Molecular Biology
[5] National Heart,undefined
[6] Lung and Blood Institute,undefined
[7] National Institutes of Health,undefined
[8] Agilent Technologies,undefined
[9] Princeton University,undefined
[10] Vascular Medicine Research Unit,undefined
[11] Brigham and Women's Hospital and Harvard Medical School,undefined
[12] Present addresses: Constellation Pharmaceuticals,undefined
[13] 148 Sidney Street,undefined
[14] Cambridge,undefined
[15] Massachusetts 02139,undefined
[16] USA (M.S.; F.L.); Department of Pathology,undefined
[17] Beth Israel Deaconess Medical Center,undefined
[18] Harvard Medical School,undefined
[19] Boston,undefined
[20] Massachusetts 02115,undefined
[21] USA (M.H.); Department of Biology,undefined
[22] Texas A&M University,undefined
[23] College Station,undefined
[24] Texas 77843,undefined
[25] USA (N.K.Y.).,undefined
来源
Nature | 2010年 / 466卷
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摘要
Mutations in the PHF8 gene, which encodes the plant homeo domain (PHD) finger protein 8, are connected to X-linked mental retardation associated with cleft lip and cleft palate. Two groups now report that the PHF8 protein is a histone demethylase with activity against H4K20me1 (histone H4 lysine 20). Qi et al. report a role for PHF8 in regulating gene expression, as well as in neuronal cell survival and craniofacial development in zebrafish. The results suggest there may be a link between histone methylation dynamics and X-linked mental retardation. Liu et al. show that PHF8 is linked to two distinct events during cell-cycle progression. PHF8 is recruited to the promoters of G1/S-phase genes where it removes H4K20me1 and contributes to gene activation, whereas dissociation of PHF8 from chromatin in prophase allows H4K20me1 to accumulate during mitosis.
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页码:503 / 507
页数:4
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