Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease

被引:514
作者
Cloos, Paul A. C. [1 ]
Christensen, Jesper
Agger, Karl
Helin, Kristian
机构
[1] Univ Copenhagen, Biotech Res & Innovat Ctr BRIC, DK-2200 Copenhagen, Denmark
关键词
cancer; differentiation; demethylases; epigenetic; histone; JmjC;
D O I
10.1101/gad.1652908
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The enzymes catalyzing lysine and arginine methylation of histones are essential for maintaining transcriptional programs and determining cell fate and identity. Until recently, histone methylation was regarded irreversible. However, within the last few years, several families of histone demethylases erasing methyl marks associated with gene repression or activation have been identified, underscoring the plasticity and dynamic nature of histone methylation. Recent discoveries have revealed that histone demethylases take part in large multiprotein complexes synergizing with histone deacetylases, histone methyltransferases, and nuclear receptors to control developmental and transcriptional programs. Here we review the emerging biochemical and biological functions of the histone demethylases and discuss their potential involvement in human diseases, including cancer.
引用
收藏
页码:1115 / 1140
页数:26
相关论文
共 179 条
  • [81] The retinoblastoma binding protein RBP2 is an H3K4 demethylase
    Klose, Robert J.
    Yan, Qin
    Tothova, Zuzana
    Yamane, Kenichi
    Erdjument-Bromage, Hediye
    Tempst, Paul
    Gilliland, D. Gary
    Zhang, Yi
    Kaelin, William G., Jr.
    [J]. CELL, 2007, 128 (05) : 889 - 900
  • [82] JmjC-domain-containing proteins and histone demethylation
    Klose, Robert J.
    Kallin, Eric M.
    Zhang, Yi
    [J]. NATURE REVIEWS GENETICS, 2006, 7 (09) : 715 - 727
  • [83] The transcriptional repressor JHDM3A demethylates trimethyl histone H3 lysine 9 and lysine 36
    Klose, Robert J.
    Yamane, Kenichi
    Bae, Yangjin
    Zhang, Dianzheng
    Erdjument-Bromage, Hediye
    Tempst, Paul
    Wong, Jiemin
    Zhang, Yi
    [J]. NATURE, 2006, 442 (7100) : 312 - 316
  • [84] Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate
    Koivisto, A. M.
    Ala-Mello, S.
    Lemmela, S.
    Komu, H. A.
    Rautio, J.
    Jarvela, I.
    [J]. CLINICAL GENETICS, 2007, 72 (02) : 145 - 149
  • [85] Chromatin modifications and their function
    Kouzarides, Tony
    [J]. CELL, 2007, 128 (04) : 693 - 705
  • [86] The F-box protein Fbl10 is a novel transcriptional repressor of c-Jun
    Koyama-Nasu, Ryo
    David, Gregory
    Tanese, Naoko
    [J]. NATURE CELL BIOLOGY, 2007, 9 (09) : 1074 - U49
  • [87] Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins
    Lachner, M
    O'Carroll, N
    Rea, S
    Mechtler, K
    Jenuwein, T
    [J]. NATURE, 2001, 410 (6824) : 116 - 120
  • [88] Recognition of unmethylated histone H3 lysine 4 links BHC80 to LSD1-mediated gene repression
    Lan, Fei
    Collins, Robert E.
    De Cegli, Rossella
    Alpatov, Roman
    Horton, John R.
    Shi, Xiaobing
    Gozani, Or
    Cheng, Xiaodong
    Shi, Yang
    [J]. NATURE, 2007, 448 (7154) : 718 - U14
  • [89] A histone H3 lysine 27 demethylase regulates animal posterior development
    Lan, Fei
    Bayliss, Peter E.
    Rinn, John L.
    Whetstine, Johnathan R.
    Wang, Jordon K.
    Chen, Shuzhen
    Iwase, Shigeki
    Alpatov, Roman
    Issaeva, Irina
    Canaani, Eli
    Roberts, Thomas M.
    Chang, Howard Y.
    Shi, Yang
    [J]. NATURE, 2007, 449 (7163) : 689 - U3
  • [90] S-pombe LSD1 homologs regulate heterochromatin propagation and euchromatic gene transcription
    Lan, Fei
    Zaratiegui, Mikel
    Villen, Judit
    Vaughn, Matthew W.
    Verdel, Andre
    Huarte, Maite
    Shi, Yujiang
    Gygi, Steven P.
    Moazed, Danesh
    Martienssen, Robert A.
    Shi, Yang
    [J]. MOLECULAR CELL, 2007, 26 (01) : 89 - 101