TY - JOUR
T1 - A cyclin B homolog in S. cerevisiae
T2 - Chronic activation of the Cdc28 protein kinase by cyclin prevents exit from mitosis
AU - Ghiara, Jayant B.
AU - Richardson, Helena E.
AU - Sugimoto, Katsunori
AU - Henze, Martha
AU - Lew, Daniel J.
AU - Wittenberg, Curt
AU - Reed, Steven I.
N1 - Funding Information:
We are very grateful to Dr. Pat O'Farrell for supplying laboratory space, material, and moral support to H. E. R. in the course of some of these investigations. We thank Don McQuitty and the flow cytometry group at Scripps Clinic for their invaluable help. We would also like to thank Dr. Gary Cole for a critical reading of this manuscript. D. J. L. acknowledges the support of a Damon Runyon-Walter Winchell Cancer Foundation Fellowship. S. I. R. and C. W. acknowledge support from Public Health Service grants GM38328 and GM43487, respectively.
PY - 1991/4/5
Y1 - 1991/4/5
N2 - A cyclin B homolog was identified in Saccharomyces cerevisiae using degenerate oligonucleotides and the polymerase chain reaction. The protein, designated Scb1, has a high degree of similarity with B-type cyclins from organisms ranging from fission yeast to human. Levels of SCB1 mRNA and protein were found to be periodic through the cell cycle, with maximum accumulation late, most likely in the G2 interval. Deletion of the gene was found not to be lethal, and subsequently other B-type cyclins have been found in yeast functionally redundant with Scb1. A mutant allele of SCB1 that removes an amino-terminal fragment of the encoded protein thoughtto be required for efficient degradation during mitosis confers a mitotic arrest phenotype. This arrest can be reversed by inactivation of the Cdc28 protein kinase, suggesting that cyclin-mediated arrest results from persistent protein kinase activation.
AB - A cyclin B homolog was identified in Saccharomyces cerevisiae using degenerate oligonucleotides and the polymerase chain reaction. The protein, designated Scb1, has a high degree of similarity with B-type cyclins from organisms ranging from fission yeast to human. Levels of SCB1 mRNA and protein were found to be periodic through the cell cycle, with maximum accumulation late, most likely in the G2 interval. Deletion of the gene was found not to be lethal, and subsequently other B-type cyclins have been found in yeast functionally redundant with Scb1. A mutant allele of SCB1 that removes an amino-terminal fragment of the encoded protein thoughtto be required for efficient degradation during mitosis confers a mitotic arrest phenotype. This arrest can be reversed by inactivation of the Cdc28 protein kinase, suggesting that cyclin-mediated arrest results from persistent protein kinase activation.
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U2 - 10.1016/0092-8674(91)90417-W
DO - 10.1016/0092-8674(91)90417-W
M3 - Article
C2 - 1849458
AN - SCOPUS:0025777453
SN - 0092-8674
VL - 65
SP - 163
EP - 174
JO - Cell
JF - Cell
IS - 1
ER -