Fission yeast cut1 and cut2 are essential for sister chromatid separation, concentrate along the metaphase spindle and form large complexes

被引:167
作者
Funabiki, H
Kumada, K
Yanagida, M
机构
[1] Department of Biophysics, Graduate School of Science, Kyoto University, Sakyo-ku
关键词
anaphase; checkpoint control; cyclosome-APC; spindle; ubiquitin-dependent proteolysis;
D O I
10.1002/j.1460-2075.1996.tb01052.x
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
Fission yeast Schizosaccharomyces pombe temperature-sensitive (ts) cut1 mutants fail to separate sister chromatids in anaphase but the cells continue to divide, leading to bisection of the undivided nucleus (the cut phenotype). If cytokinesis is blocked, replication continues, forming a giant nucleus with polyploid chromosomes, We show here that the phenotype of ts cut2-364 is highly similar to that of cut1 and that the functions of the gene products of cut1(+) and cut2(+) are closely interrelated. The cut1(+) and cut2(+) genes are essential for viability and interact genetically. Cut1 protein concentrates along the short spindle in metaphase as does Cut2. Cut1 (similar to 200 kDa) and Cut2 (42 kDa) associate, as shown by immunoprecipitation, and cosediment as large complexes (30 and 40S) in sucrose gradient centrifugation, Their behavior in the cell cycle is strikingly different, however: Cut2 is degraded in anaphase by the same proteolytic machinery used for the destruction of cyclin B, whereas Cut1 exists throughout the cell cycle. The essential function of the Cut1-Cut2 complex which ensures sister chromatid separation may be regulated by Cut2 proteolysis. The C-terminal region of Cut1 is evolutionarily conserved and similar to that of budding yeast Esp1, filamentous fungi BimB and a human protein.
引用
收藏
页码:6617 / 6628
页数:12
相关论文
共 61 条
[1]   CLONING AND MANIPULATION OF THE SCHIZOSACCHAROMYCES-POMBE HIS7+ GENE AS A NEW SELECTABLE MARKER FOR MOLECULAR-GENETIC STUDIES [J].
APOLINARIO, E ;
NOCERO, M ;
JIN, M ;
HOFFMAN, CS .
CURRENT GENETICS, 1993, 24 (06) :491-495
[2]   A YEAST GENE ESSENTIAL FOR REGULATION OF SPINDLE POLE DUPLICATION [J].
BAUM, P ;
YIP, C ;
GOETSCH, L ;
BYERS, B .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (12) :5386-5397
[3]   CYCLIN-LIKE ACCUMULATION AND LOSS OF THE PUTATIVE KINETOCHORE MOTOR CENP-E RESULTS FROM COUPLING CONTINUOUS SYNTHESIS WITH SPECIFIC DEGRADATION AT THE END OF MITOSIS [J].
BROWN, KD ;
COULSON, RMR ;
YEN, TJ ;
CLEVELAND, DW .
JOURNAL OF CELL BIOLOGY, 1994, 125 (06) :1303-1312
[4]  
CREANOR J, 1990, J CELL SCI, V96, P435
[5]   MITOSIS [J].
EARNSHAW, WC ;
PLUTA, AF .
BIOESSAYS, 1994, 16 (09) :639-643
[6]   PURIFICATION OF A RAS-RESPONSIVE ADENYLYL CYCLASE COMPLEX FROM SACCHAROMYCES-CEREVISIAE BY USE OF AN EPITOPE ADDITION METHOD [J].
FIELD, J ;
NIKAWA, J ;
BROEK, D ;
MACDONALD, B ;
RODGERS, L ;
WILSON, IA ;
LERNER, RA ;
WIGLER, M .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2159-2165
[7]   CELL CYCLE-DEPENDENT SPECIFIC POSITIONING AND CLUSTERING OF CENTROMERES AND TELOMERES IN FISSION YEAST [J].
FUNABIKI, H ;
HAGAN, I ;
UZAWA, S ;
YANAGIDA, M .
JOURNAL OF CELL BIOLOGY, 1993, 121 (05) :961-976
[8]   Cut2 proteolysis required for sister-chromatid separation in fission yeast [J].
Funabiki, H ;
Yamano, H ;
Kumada, K ;
Nagao, K ;
Hunt, T ;
Yanagida, M .
NATURE, 1996, 381 (6581) :438-441
[9]   SACCHAROMYCES-CEREVISIAE 26S PROTEASE MUTANTS ARREST CELL-DIVISION IN G2/METAPHASE [J].
GHISLAIN, M ;
UDVARDY, A ;
MANN, C .
NATURE, 1993, 366 (6453) :358-362
[10]  
GLOTZER M, 1991, NATURE, V349, P132, DOI 10.1038/349132a0