TY - JOUR
T1 - Regulation of the centrosome cycle
AU - Fujita, Hiroki
AU - Yoshino, Yuki
AU - Chiba, Natsuko
N1 - Funding Information:
This study was supported by grants-in-aid from the Ministry of Education, Culture Sports, Science and Technology, Japan Society for the Promotion of Science (JSPS KAKENHI Grant Numbers (24300327, 25640086), Project for Development of Innovative Research on Cancer Therapeutics (P-DIRECT), Program for interdisciplinary research in Frontier Research Institute for Interdisciplinary Sciences (FRIS), Tohoku University, the Takeda Science Foundation, Astellas Foundation for Research on Metabolic Disorders, the Yasuda Medical Foundation and the Princess Takamatsu Cancer Research Fund (14-24621).
Publisher Copyright:
© 2016, © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC. © 2016, © Hiroki Fujita, Yuki Yoshino, and Natsuko Chiba.
PY - 2016/3/3
Y1 - 2016/3/3
N2 - The centrosome, consisting of mother and daughter centrioles surrounded by the pericentriolar matrix (PCM), functions primarily as a microtubule organizing center (MTOC) in most animal cells. In dividing cells the centrosome duplicates once per cell cycle and its number and structure are highly regulated during each cell cycle to organize an effective bipolar spindle in the mitotic phase. Defects in the regulation of centrosome duplication lead to a variety of human diseases, including cancer, through abnormal cell division and inappropriate chromosome segregation. At the end of mitosis the daughter centriole disengages from the mother centriole. This centriole disengagement is an important licensing step for centrosome duplication. In S phase, one new daughter centriole forms perpendicular to each centriole. The centrosome recruits further PCM proteins in the late G2 phase and the two centrosomes separate at mitotic entry to form a bipolar spindle. Here, we summarize research findings in the field of centrosome biology, focusing on the mechanisms of regulation of the centrosome cycle in human cells.
AB - The centrosome, consisting of mother and daughter centrioles surrounded by the pericentriolar matrix (PCM), functions primarily as a microtubule organizing center (MTOC) in most animal cells. In dividing cells the centrosome duplicates once per cell cycle and its number and structure are highly regulated during each cell cycle to organize an effective bipolar spindle in the mitotic phase. Defects in the regulation of centrosome duplication lead to a variety of human diseases, including cancer, through abnormal cell division and inappropriate chromosome segregation. At the end of mitosis the daughter centriole disengages from the mother centriole. This centriole disengagement is an important licensing step for centrosome duplication. In S phase, one new daughter centriole forms perpendicular to each centriole. The centrosome recruits further PCM proteins in the late G2 phase and the two centrosomes separate at mitotic entry to form a bipolar spindle. Here, we summarize research findings in the field of centrosome biology, focusing on the mechanisms of regulation of the centrosome cycle in human cells.
KW - Cell cycle
KW - centriole
KW - centrosome
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U2 - 10.1080/23723556.2015.1075643
DO - 10.1080/23723556.2015.1075643
M3 - Review article
AN - SCOPUS:85044624466
SN - 2372-3556
VL - 3
JO - Molecular and Cellular Oncology
JF - Molecular and Cellular Oncology
IS - 2
M1 - e1075643
ER -