Ubiquitin proteasome system (UPS): what can chromatin do for you?

被引:103
作者
O'Connell, Brenda C. [1 ]
Harper, J. Wade [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.ceb.2007.02.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cul4-Ddb1, a RING H2 ubiquitin ligase, plays an important role in many vital cellular processes including DNA replication, DNA repair and transcription. Recent research reveals strong links between Cul4-mediated signaling pathways and chromatin biology. Ubiquitylation of substrates by Cul4-Ddb1 occurs on chromatin and is initiated by chromatin-based signals that either recruit Cul4-Ddb1 to chromatin or alter the activity of the ligase. This includes Cul4-mediated ubiquitylation of the replication licensing factor, Cdt1; a process that requires chromatin-bound PCNA and Cdt2, a member of the recently identified family of candidate substrate receptors for Cul4 (termed Ddb1- and Cul4-associated factors: DCAFs). The activity of two other Cul4-based ubiquitin ligases, Cul4-Ddb1(Ddb2) and Cul4-Ddb1(CSA), are differentially regulated by the COP9 signalosome in response to different chromatin-based signals. Finally, examples of direct modifications to chromatin by Cul4-Ddb1 have emerged, including ubiquitylation of histories and the recruitment of enzymes involved in chromatin remodeling or histone methylation.
引用
收藏
页码:206 / 214
页数:9
相关论文
共 56 条
[31]   Two E3 ubiquitin ligases, SCF-Skp2 and DDB1-Cul4, target human Cdt1 for proteolysis [J].
Nishitani, H ;
Sugimoto, N ;
Roukos, V ;
Nakanishi, Y ;
Saijo, M ;
Obuse, C ;
Tsurimoto, T ;
Nakayama, KI ;
Nakayama, K ;
Fujita, M ;
Lygerou, Z ;
Nishimoto, T .
EMBO JOURNAL, 2006, 25 (05) :1126-1136
[32]   Structural basis for phosphodependent substrate selection and orientation by the SCFCdc4 ubiquitin ligase [J].
Orlicky, S ;
Tang, XJ ;
Willems, A ;
Tyers, M ;
Sicheri, F .
CELL, 2003, 112 (02) :243-256
[33]   H2B ubiquitylation: the end is in sight [J].
Osley, MA .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2004, 1677 (1-3) :74-78
[34]   Evidence for a physical association of the COP9 signalosome, the proteasome, and specific SCF E3 ligases in vivo [J].
Peng, ZH ;
Shen, YP ;
Feng, SH ;
Wang, XP ;
Chitteti, BN ;
Vierstra, RD ;
Deng, XW .
CURRENT BIOLOGY, 2003, 13 (13) :R504-R505
[35]   Function and regulation of Cullin-RING ubiquitin ligases [J].
Petroski, MD ;
Deshaies, RJ .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (01) :9-20
[36]   Back to the future with ubiquitin [J].
Pickart, CM .
CELL, 2004, 116 (02) :181-190
[37]   DNA damage induces Cdt1 proteolysis in fission yeast through a pathway dependent on Cdt2 and Ddb1 [J].
Ralph, Emma ;
Boye, Erik ;
Kearsey, Stephen E. .
EMBO REPORTS, 2006, 7 (11) :1134-1139
[38]   DTL/CDT2 is essential for both CDT1 regulation and the early G2/M checkpoint [J].
Sansam, Christopher L. ;
Shepard, Jennifer L. ;
Lai, Kevin ;
Ianari, Alessandra ;
Danielian, Paul S. ;
Amsterdam, Adam ;
Hopkins, Nancy ;
Lees, Jacqueline A. .
GENES & DEVELOPMENT, 2006, 20 (22) :3117-3129
[39]   Interactions of the COP9 signalosome with the E3 ubiquitin ligase SCFTIR1 in mediating auxin response [J].
Schwechheimer, C ;
Serino, G ;
Callis, J ;
Crosby, WL ;
Lyapina, S ;
Deshaies, RJ ;
Gray, WM ;
Estelle, M ;
Deng, XW .
SCIENCE, 2001, 292 (5520) :1379-1382
[40]   PCNA is a cofactor for Cdt1 degradation by CUL4/DDB1-mediated N-terminal ubiquitination [J].
Senga, T ;
Sivaprasad, U ;
Zhu, WG ;
Park, JH ;
Arias, EE ;
Walter, JC ;
Dutta, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (10) :6246-6252