The anaphase-promoting complex: New subunits and regulators

被引:122
作者
Page, AM [1 ]
Hieter, P
机构
[1] Univ British Columbia, Ctr Mol Med & Therapeut, Vancouver, BC V5Z 4H4, Canada
[2] Johns Hopkins Univ, Sch Med, Biochem Cellular & Mol Biol Program, Baltimore, MD 21205 USA
关键词
APC; cyclosome; ubiquitination; proteolysis; cell cycle; E3; mitosis;
D O I
10.1146/annurev.biochem.68.1.583
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ubiquitin-mediated proteolysis of cell cycle regulators is a crucial process during the cell cycle. The anaphase-promoting complex (APC) is a large, multiprotein complex whose ES-ubiquitin ligase activity is required for the ubiquitination of mitotic cyclins and other regulatory proteins that are targeted for destruction during cell division. The recent identification of new APC subunits and regulatory proteins has begun to reveal some of the intricate mechanisms that govern APC regulation. One mechanism is the use of specificity factors to impose temporal control over substrate degradation. A second mechanism is the APC-mediated proteolysis of specific APC regulators. Finally, components of both the APC and the SCF E3 ubiquitin-ligase complex contain several conserved sequence motifs, including WD-40 repeats and cullin homology domains, which suggest that both complexes may use a similar mechanism for substrate ubiquitination.
引用
收藏
页码:583 / 609
页数:27
相关论文
共 126 条
[1]   Regulation of B-type cyclin proteolysis by Cdc28-associated kinases in budding yeast [J].
Amon, A .
EMBO JOURNAL, 1997, 16 (10) :2693-2702
[2]   CLOSING THE CELL-CYCLE CIRCLE IN YEAST - G2 CYCLIN PROTEOLYSIS INITIATED AT MITOSIS PERSISTS UNTIL THE ACTIVATION OF G1 CYCLINS IN THE NEXT CYCLE [J].
AMON, A ;
IRNIGER, S ;
NASMYTH, K .
CELL, 1994, 77 (07) :1037-1050
[3]   E2-C, a cyclin-selective ubiquitin carrier protein required for the destruction of mitotic cyclins [J].
Aristarkhov, A ;
Eytan, E ;
Moghe, A ;
Admon, A ;
Hershko, A ;
Ruderman, JV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :4294-4299
[4]   STRESS RESISTANCE IN SACCHAROMYCES-CEREVISIAE IS STRONGLY CORRELATED WITH ASSEMBLY OF A NOVEL TYPE OF MULTIUBIQUITIN CHAIN [J].
ARNASON, T ;
ELLISON, MJ .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) :7876-7883
[5]   ONE OF THE PROTEIN PHOSPHATASE-1 ISOENZYMES IN DROSOPHILA IS ESSENTIAL FOR MITOSIS [J].
AXTON, JM ;
DOMBRADI, V ;
COHEN, PTW ;
GLOVER, DM .
CELL, 1990, 63 (01) :33-46
[6]   The proteolysis of mitotic cyclins in mammalian cells persists from the end of mitosis until the onset of S phase [J].
Brandeis, M ;
Hunt, T .
EMBO JOURNAL, 1996, 15 (19) :5280-5289
[7]   MICROINJECTION OF MITOTIC CELLS WITH THE 3F3/2 ANTI-PHOSPHOEPITOPE ANTIBODY DELAYS THE ONSET OF ANAPHASE [J].
CAMPBELL, MS ;
GORBSKY, GJ .
JOURNAL OF CELL BIOLOGY, 1995, 129 (05) :1195-1204
[8]   The Polo-related kinase Cdc5 activates and is destroyed by the mitotic cyclin destruction machinery in S. cerevisiae [J].
Charles, JF ;
Jespersen, SL ;
Tinker-Kulberg, RL ;
Hwang, L ;
Szidon, A ;
Morgan, DO .
CURRENT BIOLOGY, 1998, 8 (09) :497-507
[9]   The transcriptional program of sporulation in budding yeast [J].
Chu, S ;
DeRisi, J ;
Eisen, M ;
Mulholland, J ;
Botstein, D ;
Brown, PO ;
Herskowitz, I .
SCIENCE, 1998, 282 (5389) :699-705
[10]   The anaphase inhibitor of Saccharomyces cerevisiae Pds1p is a target of the DNA damage checkpoint pathway [J].
Cohen-Fix, O ;
Koshland, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14361-14366