Identification of a physiological E2 module for the human anaphase-promoting complex

被引:235
作者
Williamson, Adam [1 ]
Wickliffe, Katherine E. [1 ]
Mellone, Barbara G. [1 ,2 ]
Song, Ling [1 ]
Karpen, Gary H. [1 ,2 ]
Rape, Michael [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Dept Genome Dynam, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
K11-linked chain; proteasome; ubiquitin; SPINDLE ASSEMBLY CHECKPOINT; UBIQUITIN-LIKE PROTEINS; DEPENDENT PROTEOLYSIS; MITOTIC SPINDLE; CHAIN FORMATION; KEN BOX; DEGRADATION; APC; COMPLEX/CYCLOSOME; REVEALS;
D O I
10.1073/pnas.0907887106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ubiquitination by the anaphase-promoting complex (APC/C) is essential for proliferation in all eukaryotes. The human APC/C promotes the degradation of mitotic regulators by assembling K11-linked ubiquitin chains, the formation of which is initiated by its E2 UbcH10. Here, we identify the conserved Ube2S as a K11-specific chain elongating E2 for human and Drosophila APC/C. Ube2S depends on the cell cycle-dependent association with the APC/C activators Cdc20 and Cdh1 for its activity. While depletion of Ube2S already inhibits APC/C in cells, the loss of the complete UbcH10/Ube2S-module leads to dramatic stabilization of APC/C substrates, severe spindle defects, and a strong mitotic delay. Ube2S and UbcH10 are tightly co-regulated in the cell cycle by APC/C-dependent degradation. We conclude that UbcH10 and Ube2S constitute a physiological E2-module for APC/C, the activity of which is required for spindle assembly and cell division.
引用
收藏
页码:18213 / 18218
页数:6
相关论文
共 41 条
[1]   UBXD7 binds multiple ubiquitin ligases and implicates p97 in HIF1α turnover [J].
Alexandru, Gabriela ;
Graumann, Johannes ;
Smith, Geoffrey T. ;
Kolawa, Natalie J. ;
Fang, Ruihua ;
Deshaies, Raymond J. .
CELL, 2008, 134 (05) :804-816
[2]   Novel multiubiquitin chain linkages catalyzed by the conjugating enzymes E2(EPF) and RAD6 are recognized by 26 S proteasome subunit 5 [J].
Baboshina, OV ;
Haas, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (05) :2823-2831
[3]   The END network couples spindle pole assembly to inhibition of the anaphase-promoting Complex/Cyclosome in early mitosis [J].
Ban, Kenneth H. ;
Torres, Jorge Z. ;
Miller, Julie J. ;
Mikhailov, Alexei ;
Nachury, Maxence V. ;
Tung, Jeffrey J. ;
Rieder, Conly L. ;
Jackson, Peter K. .
DEVELOPMENTAL CELL, 2007, 13 (01) :29-42
[4]   Strong inducible knockdown of APC/CCdc20 does not cause mitotic arrest in human somatic cells [J].
Baumgarten, Axel J. ;
Felthaus, Julia ;
Waesch, Ralph .
CELL CYCLE, 2009, 8 (04) :643-646
[5]   Global changes to the ubiquitin system in Huntington's disease [J].
Bennett, Eric J. ;
Shaler, Thomas A. ;
Woodman, Ben ;
Ryu, Kwon-Yul ;
Zaitseva, Tatiana S. ;
Becker, Christopher H. ;
Bates, Gillian P. ;
Schulman, Howard ;
Kopito, Ron R. .
NATURE, 2007, 448 (7154) :704-U11
[6]   UbcH10 is overexpressed in malignant breast carcinomas [J].
Berlingieri, Maria Teresa ;
Pallante, Pierlorenzo ;
Sboner, Andrea ;
Barbareschi, Mattia ;
Bianco, Mimma ;
Ferraro, Angelo ;
Mansueto, Gelsomina ;
Borbone, Eleonora ;
Guerriero, Eliana ;
Troncone, Giancarlo ;
Fusco, Alfredo .
EUROPEAN JOURNAL OF CANCER, 2007, 43 (18) :2729-2735
[7]   D box and KEN box motifs in budding yeast Hsl1p are required for APC-mediated degradation and direct binding to Cdc20p and Cdh1p [J].
Burton, JL ;
Solomon, MJ .
GENES & DEVELOPMENT, 2001, 15 (18) :2381-2395
[8]   Structural mechanisms underlying posttranslational modification by ubiquitin-like proteins [J].
Dye, Billy T. ;
Schulman, Brenda A. .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2007, 36 :131-150
[9]   Mms2-Ubc13 covalently bound to ubiquitin reveals the structural basis of linkage-specific polyubiquitin chain formation [J].
Eddins, Michael J. ;
Carlile, Candice M. ;
Gomez, Kamila M. ;
Pickart, Cecile M. ;
Wolberger, Cynthia .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (10) :915-920
[10]  
FUJITA T, 2008, CANCER SCI, DOI DOI 10.1111/J.1349-7006.2008.01026