TY - JOUR
T1 - Novel response to microtubule perturbation in meiosis
AU - Hochwagen, Andreas
AU - Wrobel, Gunnar
AU - Cartron, Marie
AU - Demougin, Philippe
AU - Niederhauser-Wiederkehr, Christa
AU - Boselli, Monica G.
AU - Primig, Michael
AU - Amon, Angelika
PY - 2005/6
Y1 - 2005/6
N2 - During the mitotic cell cycle, microtubule depolymerization leads to a cell cycle arrest in metaphase, due to activation of the spindle checkpoint. Here, we show that under microtubule-destabilizing conditions, such as low temperature or the presence of the spindle-depolymerizing drug benomyl, meiotic budding yeast cells arrest in G1 or G2, instead of metaphase. Cells arrest in G1 if microtubule perturbation occurs as they enter the meiotic cell cycle and in G2 if cells are already undergoing premeiotic S phase. Concomitantly, cells down-regulate genes required for cell cycle progression, meiotic differentiation, and spore formation in a highly coordinated manner. Decreased expression of these genes is likely to be responsible for halting both cell cycle progression and meiotic development. Our results point towards the existence of a novel surveillance mechanism of microtubule integrity that may be particularly important during specialized cell cycles when coordination of cell cycle progression with a developmental program is necessary.
AB - During the mitotic cell cycle, microtubule depolymerization leads to a cell cycle arrest in metaphase, due to activation of the spindle checkpoint. Here, we show that under microtubule-destabilizing conditions, such as low temperature or the presence of the spindle-depolymerizing drug benomyl, meiotic budding yeast cells arrest in G1 or G2, instead of metaphase. Cells arrest in G1 if microtubule perturbation occurs as they enter the meiotic cell cycle and in G2 if cells are already undergoing premeiotic S phase. Concomitantly, cells down-regulate genes required for cell cycle progression, meiotic differentiation, and spore formation in a highly coordinated manner. Decreased expression of these genes is likely to be responsible for halting both cell cycle progression and meiotic development. Our results point towards the existence of a novel surveillance mechanism of microtubule integrity that may be particularly important during specialized cell cycles when coordination of cell cycle progression with a developmental program is necessary.
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U2 - 10.1128/MCB.25.11.4767-4781.2005
DO - 10.1128/MCB.25.11.4767-4781.2005
M3 - Article
C2 - 15899877
AN - SCOPUS:18944381109
SN - 0270-7306
VL - 25
SP - 4767
EP - 4781
JO - Molecular and cellular biology
JF - Molecular and cellular biology
IS - 11
ER -