Budding yeast Bub2 is localized at spindle pole bodies and activates the mitotic checkpoint via a different pathway from Mad2

• Published in: The Journal of cell biology 1999-05, Vol.145 (5), p.979-991
• Main Authors: Fraschini, R, Formenti, E, Lucchini, G, Piatti, S
• Format: Article
• Language: English
• Subjects: Anaphase; anaphase-promoting complex; azoles; binding; binding proteins; Calcium-Binding Proteins - physiology; Carrier Proteins; Cell cycle; Cell Cycle Proteins; Cells; Cellular biology; Chromatids; Chromosomes; Cyclins; Cyclins - physiology; deletions; Fungal Proteins - physiology; immunocytochemistry; Kinetochores; Mad2 Proteins; microtubules; Mitosis; Mitosis - physiology; mutants; nocodazole; Nuclear Proteins; organelles; Proteins; Regular; Saccharomyces cerevisiae; Saccharomyces cerevisiae - cytology; Saccharomyces cerevisiae - physiology; Saccharomyces cerevisiae Proteins; Saccharomycetales; Signal Transduction; Yeast; Yeasts
• ISSN: 0021-9525; 1540-8140
• DOI: 10.1083/jcb.145.5.979

The mitotic checkpoint blocks cell cycle progression before anaphase in case of mistakes in the alignment of chromosomes on the mitotic spindle. In budding yeast, the Mad1, 2, 3, and Bub1, 2, 3 proteins mediate this arrest. Vertebrate homologues of Mad1, 2, 3, and Bub1, 3 bind to unattached kinetochores and prevent progression through mitosis by inhibiting Cdc20/APC-mediated proteolysis of anaphase inhibitors, like Pds1 and B-type cyclins. We investigated the role of Bub2 in budding yeast mitotic checkpoint. The following observations indicate that Bub2 and Mad1, 2 probably activate the checkpoint via different pathways: (a) unlike the other Mad and Bub proteins, Bub2 localizes at the spindle pole body (SPB) throughout the cell cycle; (b) the effect of concomitant lack of Mad1 or Mad2 and Bub2 is additive, since nocodazole-treated mad1 bub2 and mad2 bub2 double mutants rereplicate DNA more rapidly and efficiently than either single mutant; (c) cell cycle progression of bub2 cells in the presence of nocodazole requires the Cdc26 APC subunit, which, conversely, is not required for mad2 cells in the same conditions. Altogether, our data suggest that activation of the mitotic checkpoint blocks progression through mitosis by independent and partially redundant mechanisms.