Histone demethylase KDM5A is an integral part of the core Notch-RBP-J repressor complex

被引:139
作者
Liefke, Robert [1 ]
Oswald, Franz [2 ]
Alvarado, Cristobal [2 ]
Ferres-Marco, Dolores [3 ]
Mittler, Gerhard [1 ]
Rodriguez, Patrick [1 ]
Dominguez, Maria [3 ]
Borggrefe, Tilman [1 ]
机构
[1] Max Planck Inst Immunobiol, D-79108 Freiburg, Germany
[2] Univ Ulm, Dept Internal Med 1, D-89081 Ulm, Germany
[3] Univ Miguel Hernandez, CSIC, Inst Neurociencias, E-03550 Alicante, Spain
关键词
Histone demethylase; RBP-J; Notch target gene repression; T cells; Drosophila; tumorigenesis; LITTLE-IMAGINAL-DISCS; GENOME-WIDE ANALYSIS; H3K4; DEMETHYLASE; J-KAPPA; BINDING; TARGET; GENE; ACTIVATION; GROWTH; EYE;
D O I
10.1101/gad.563210
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Timely acquisition of cell fates and the elaborate control of growth in numerous organs depend on Notch signaling. Upon ligand binding, the core transcription factor RBP-J activates transcription of Notch target genes. In the absence of signaling, RBP-J switches off target gene expression, assuring the tight spatiotemporal control of the response by a mechanism incompletely understood. Here we show that the histone demethylase KDM5A is an integral, conserved component of Notch/RBP-J gene silencing. Methylation of histone H3 Lys 4 is dynamically erased and re-established at RBP-J sites upon inhibition and reactivation of Notch signaling. KDM5A interacts physically with RBP-J; this interaction is conserved in Drosophila and is crucial for Notch-induced growth and tumorigenesis responses.
引用
收藏
页码:590 / 601
页数:12
相关论文
共 52 条
[1]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[2]   Genome-wide mapping and analysis of active promoters in mouse embryonic stem cells and adult organs [J].
Barrera, Leah O. ;
Li, Zirong ;
Smith, Andrew D. ;
Arden, Karen C. ;
Cavenee, Webster K. ;
Zhang, Michael Q. ;
Green, Roland D. ;
Ren, Bing .
GENOME RESEARCH, 2008, 18 (01) :46-59
[3]   High-resolution profiling of histone methylations in the human genome [J].
Barski, Artern ;
Cuddapah, Suresh ;
Cui, Kairong ;
Roh, Tae-Young ;
Schones, Dustin E. ;
Wang, Zhibin ;
Wei, Gang ;
Chepelev, Iouri ;
Zhao, Keji .
CELL, 2007, 129 (04) :823-837
[4]   Binding of pRB to the PHD protein RBP2 promotes cellular differentiation [J].
Benevolenskaya, EV ;
Murray, HL ;
Branton, P ;
Young, RA ;
Kaelin, WG .
MOLECULAR CELL, 2005, 18 (06) :623-635
[5]   The Notch signaling pathway: Transcriptional regulation at Notch target genes [J].
Borggrefe, T. ;
Oswald, F. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2009, 66 (10) :1631-1646
[6]   Bre1 is required for notch signaling and histone modification [J].
Bray, S ;
Musisi, H ;
Bienz, M .
DEVELOPMENTAL CELL, 2005, 8 (02) :279-286
[7]   Notch signalling: a simple pathway becomes complex [J].
Bray, Sarah J. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2006, 7 (09) :678-689
[8]   RBP2 belongs to a family of demethylases, specific for tri- and dimethylated lysine 4 on histone 3 [J].
Christensen, Jesper ;
Agger, Karl ;
Cloos, Paul A. C. ;
Pasini, Diego ;
Rose, Simon ;
Sennels, Lau ;
Rappsilber, Juri ;
Hansen, Klaus H. ;
Salcini, Anna Elisabetta ;
Helin, Kristian .
CELL, 2007, 128 (06) :1063-1076
[9]   Organ specification-growth control connection:: New in-sights from the Drosophila eye-antennal disc [J].
Domínguez, M ;
Casares, F .
DEVELOPMENTAL DYNAMICS, 2005, 232 (03) :673-684
[10]   Growth and specification of the eye are controlled independently by Eyegone and Eyeless in Drosophila melanogaster [J].
Dominguez, M ;
Ferres-Marco, D ;
Gutierrez-Aviño, FJ ;
Speicher, SA ;
Beneyto, M .
NATURE GENETICS, 2004, 36 (01) :31-39