Fission yeast Cut2 required for anaphase has two destruction boxes

被引:65
作者
Funabiki, H
Yamano, H
Nagao, K
Tanaka, H
Yasuda, H
Hunt, T
Yanagida, M
机构
[1] KYOTO UNIV,GRAD SCH SCI,DEPT BIOPHYS,SAKYO KU,KYOTO 606,JAPAN
[2] IMPERIAL CANC RES FUND,CLARE HALL LABS,S MIMMS EN6 3LD,HERTS,ENGLAND
[3] TOKYO UNIV PHARM & LIFE SCI,HACHIOJI,TOKYO 19203,JAPAN
关键词
anaphase; APC-cyclosome; cyclin; destruction box; mitosis;
D O I
10.1093/emboj/16.19.5977
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
The fission yeast Schizosaccharomyces pombe cut2(+) gene is essential for sister chromatid separation, Cut2 protein, which locates in the interphase nucleus and along the metaphase spindle, disappears in anaphase with the same timing as mitotic cyclin destruction, This proteolysis depends on the APC (Anaphase-Promoting Complex)-cyclosome which contains ubiquitin ligase activity, The N-terminus of Cut2 contains two stretches similar to the mitotic cyclin destruction box. We show that both sequences (33RAPLGSTKQ and 52RTV-LGGKST) serve as destruction boxes and are required for in vitro polyubiquitination and proteolysis, Cut2 with doubly mutated destruction boxes inhibits anaphase, whereas Cut2 with singly mutated boxes can suppress cut2 mutations, Strong expression of the N-terminal 73 residues containing the destruction boxes leads to the accumulation of endogenous cyclin and Cut2, and arrests cells in metaphase, whereas the same fragment with the mutated boxes does not, Cut2 proteolysis occurs in vitro using Xenopus mitotic extracts in the presence of functional destruction boxes, Furthermore, Cut2 is polyubiquitinated in an in vitro system using HeLa extracts, and this polyubiquitination requires the destruction boxes.
引用
收藏
页码:5977 / 5987
页数:11
相关论文
共 48 条
[11]  
HAGAN IM, 1988, J CELL SCI, V89, P343
[12]   Lessons from the discovery of the ubiquitin system [J].
Hershko, A .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (11) :445-449
[13]   A TEMPERATURE-SENSITIVE MUTATION OF THE SCHIZOSACCHAROMYCES-POMBE GENE NUC2+THAT ENCODES A NUCLEAR SCAFFOLD-LIKE PROTEIN BLOCKS SPINDLE ELONGATION IN MITOTIC ANAPHASE [J].
HIRANO, T ;
HIRAOKA, Y ;
YANAGIDA, M .
JOURNAL OF CELL BIOLOGY, 1988, 106 (04) :1171-1183
[14]   ISOLATION AND CHARACTERIZATION OF SCHIZOSACCHAROMYCES-POMBE CUT MUTANTS THAT BLOCK NUCLEAR DIVISION BUT NOT CYTOKINESIS [J].
HIRANO, T ;
FUNAHASHI, S ;
UEMURA, T ;
YANAGIDA, M .
EMBO JOURNAL, 1986, 5 (11) :2973-2979
[15]   ANAPHASE IS INITIATED BY PROTEOLYSIS RATHER THAN BY THE INACTIVATION OF MATURATION-PROMOTING FACTOR [J].
HOLLOWAY, SL ;
GLOTZER, M ;
KING, RW ;
MURRAY, AW .
CELL, 1993, 73 (07) :1393-1402
[16]   MOUSE P87(WEE1) KINASE IS REGULATED BY M-PHASE SPECIFIC PHOSPHORYLATION [J].
HONDA, R ;
TANAKA, H ;
OHBA, Y ;
YASUDA, H .
CHROMOSOME RESEARCH, 1995, 3 (05) :300-308
[17]   THE REQUIREMENTS FOR PROTEIN-SYNTHESIS AND DEGRADATION, AND THE CONTROL OF DESTRUCTION OF CYCLIN-A AND CYCLIN-B IN THE MEIOTIC AND MITOTIC CELL-CYCLES OF THE CLAM EMBRYO [J].
HUNT, T ;
LUCA, FC ;
RUDERMAN, JV .
JOURNAL OF CELL BIOLOGY, 1992, 116 (03) :707-724
[18]   GENES INVOLVED IN SISTER-CHROMATID SEPARATION ARE NEEDED FOR B-TYPE CYCLIN PROTEOLYSIS IN BUDDING YEAST [J].
IRNIGER, S ;
PIATTI, S ;
MICHAELIS, C ;
NASMYTH, K .
CELL, 1995, 81 (02) :269-278
[19]   APC-mediated proteolysis of Ase 1 and the morphogenesis of the mitotic spindle [J].
Juang, YL ;
Huang, J ;
Peters, JM ;
McLaughlin, ME ;
Tai, CY ;
Pellman, D .
SCIENCE, 1997, 275 (5304) :1311-1314
[20]   A 20S COMPLEX CONTAINING CDC27 AND CDC16 CATALYZES THE MITOSIS-SPECIFIC CONJUGATION OF UBIQUITIN TO CYCLIN-B [J].
KING, RW ;
PETERS, JM ;
TUGENDREICH, S ;
ROLFE, M ;
HIETER, P ;
KIRSCHNER, MW .
CELL, 1995, 81 (02) :279-288