CHARACTERIZATION OF 4 B-TYPE CYCLIN GENES OF THE BUDDING YEAST SACCHAROMYCES-CEREVISIAE

被引:263
作者
FITCH, I
DAHMANN, C
SURANA, U
AMON, A
NASMYTH, K
GOETSCH, L
BYERS, B
FUTCHER, B
机构
[1] RES INST MOLEC PATHOL, A-1030 VIENNA, AUSTRIA
[2] UNIV WASHINGTON, DEPT GENET, SEATTLE, WA 98195 USA
关键词
D O I
10.1091/mbc.3.7.805
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The previously described CLB1 and CLB2 genes encode a closely related pair of B-type cyclins. Here we present the sequences of another related pair of B-type cyclin genes, which we term CLB3 and CLB4. Although CLB1 and CLB2 mRNAs rise in abundance at the time of nuclear division, CLB3 and CLB4 are turned on earlier, rising early in S phase and declining near the end of nuclear division. When all possible single and multiple deletion mutants were constructed, some multiple mutations were lethal, whereas all single mutants were viable. All lethal combinations included the clb2 deletion, whereas the clb1 clb3 clb4 triple mutant was viable, suggesting a key role for CLB2. The inviable multiple clb mutants appeared to have a defect in mitosis. Conditional clb mutants arrested as large budded cells with a G2 DNA content but without any mitotic spindle. Electron microscopy showed that the spindle pole bodies had duplicated but not separated, and no spindle had formed. This suggests that the Clb/Cdc28 kinase may have a relatively direct role in spindle formation. The two groups of Clbs may have distinct roles in spindle formation and elongation.
引用
收藏
页码:805 / 818
页数:14
相关论文
共 51 条
[1]   REGULATION OF P34CDC28 TYROSINE PHOSPHORYLATION IS NOT REQUIRED FOR ENTRY INTO MITOSIS IN SACCHAROMYCES-CEREVISIAE [J].
AMON, A ;
SURANA, U ;
MUROFF, I ;
NASMYTH, K .
NATURE, 1992, 355 (6358) :368-371
[2]   INVOLVEMENT OF CDC13+ IN MITOTIC CONTROL IN SCHIZOSACCHAROMYCES-POMBE - POSSIBLE INTERACTION OF THE GENE-PRODUCT WITH MICROTUBULES [J].
BOOHER, R ;
BEACH, D .
EMBO JOURNAL, 1988, 7 (08) :2321-2327
[3]   THE FISSION YEAST CDC2 CDC13 SUC1 PROTEIN-KINASE - REGULATION OF CATALYTIC ACTIVITY AND NUCLEAR-LOCALIZATION [J].
BOOHER, RN ;
ALFA, CE ;
HYAMS, JS ;
BEACH, DH .
CELL, 1989, 58 (03) :485-497
[4]   A FISSION YEAST B-TYPE CYCLIN FUNCTIONING EARLY IN THE CELL-CYCLE [J].
BUENO, A ;
RICHARDSON, H ;
REED, SI ;
RUSSELL, P .
CELL, 1991, 66 (01) :149-159
[5]   DUPLICATION OF SPINDLE PLAQUES AND INTEGRATION OF YEAST-CELL CYCLE [J].
BYERS, B ;
GOETSCH, L .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1973, 38 :123-131
[6]  
BYERS B, 1981, MOL BIOL YEAST SACCH, P97
[7]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[8]   ISOLATION AND CHARACTERIZATION OF CDNA CLONES ENCODING A FUNCTIONAL P34CDC2 HOMOLOG FROM ZEA-MAYS [J].
COLASANTI, J ;
TYERS, M ;
SUNDARESAN, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (08) :3377-3381
[9]   ACTIVATION OF CDC2 PROTEIN-KINASE DURING MITOSIS IN HUMAN-CELLS - CELL-CYCLE DEPENDENT PHOSPHORYLATION AND SUBUNIT REARRANGEMENT [J].
DRAETTA, G ;
BEACH, D .
CELL, 1988, 54 (01) :17-26
[10]   CDC2 PROTEIN-KINASE IS COMPLEXED WITH BOTH CYCLIN-A AND CYCLIN-B - EVIDENCE FOR PROTEOLYTIC INACTIVATION OF MPF [J].
DRAETTA, G ;
LUCA, F ;
WESTENDORF, J ;
BRIZUELA, L ;
RUDERMAN, J ;
BEACH, D .
CELL, 1989, 56 (05) :829-838