TY - JOUR
T1 - Two distinct cytokinesis pathways drive trypanosome cell division initiation from opposite cell ends
AU - Zhou, Qing
AU - Gu, Jianhua
AU - Lun, Zhao Rong
AU - Ayala, Francisco J.
AU - Li, Ziyin
N1 - Funding Information:
ACKNOWLEDGMENTS: We thank Drs. Arthur Günzl, Christopher de Graffenried, and Cynthia He for providing the epitope tagging vectors, the PS54 antibody, and the anti-CC2D antibody, respectively. This work was supported by NIH R01 Grant AI101437 (to Z.L.); National Natural Science Foundation of China Grant 31472058; and Natural Science Foundation of Guangdong Province Grant 2015A030311042 (to Z.-R.L.).
PY - 2016/3/22
Y1 - 2016/3/22
N2 - Cytokinesis in Trypanosoma brucei, an early branching protozoan, occurs along its longitudinal axis uni-directionally from the anterior tip of the new flagellum attachment zone filament toward the cell's posterior end. However, the underlying mechanisms remain elusive. Here we report that cytokinesis in T. brucei is regulated by a concerted action of Polo-like kinase, Aurora B kinase, and a trypanosome- specific protein CIF1. Phosphorylation of CIF1 by Polo-like kinase targets it to the anterior tip of the new flagellum attachment zone filament, where it subsequently recruits Aurora B kinase to initiate cytokinesis. Consistent with its role, CIF1 depletion inhibits cytokinesis initiation from the anterior end of the cell, but, surprisingly, triggers cytokinesis initiation from the posterior end of the cell, suggesting the activation of an alternative cytokinesis from the opposite cell end. Our results reveal the mechanistic roles of CIF1 and Polo-like kinase in cytokinesis initiation and elucidate the mechanism underlying the recruitment of Aurora B kinase to the cytokinesis initiation site at late anaphase. These findings also delineate a signaling cascade controlling cytokinesis initiation from the anterior end of the cell and uncover a backup cytokinesis that is initiated from the posterior end of the cell when the typical anterior-to-posterior cytokinesis is compromised.
AB - Cytokinesis in Trypanosoma brucei, an early branching protozoan, occurs along its longitudinal axis uni-directionally from the anterior tip of the new flagellum attachment zone filament toward the cell's posterior end. However, the underlying mechanisms remain elusive. Here we report that cytokinesis in T. brucei is regulated by a concerted action of Polo-like kinase, Aurora B kinase, and a trypanosome- specific protein CIF1. Phosphorylation of CIF1 by Polo-like kinase targets it to the anterior tip of the new flagellum attachment zone filament, where it subsequently recruits Aurora B kinase to initiate cytokinesis. Consistent with its role, CIF1 depletion inhibits cytokinesis initiation from the anterior end of the cell, but, surprisingly, triggers cytokinesis initiation from the posterior end of the cell, suggesting the activation of an alternative cytokinesis from the opposite cell end. Our results reveal the mechanistic roles of CIF1 and Polo-like kinase in cytokinesis initiation and elucidate the mechanism underlying the recruitment of Aurora B kinase to the cytokinesis initiation site at late anaphase. These findings also delineate a signaling cascade controlling cytokinesis initiation from the anterior end of the cell and uncover a backup cytokinesis that is initiated from the posterior end of the cell when the typical anterior-to-posterior cytokinesis is compromised.
KW - Aurora B kinase
KW - Backup cytokinesis
KW - Cytokinesis
KW - Polo-like kinase
KW - Trypanosoma brucei
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U2 - 10.1073/pnas.1601596113
DO - 10.1073/pnas.1601596113
M3 - Article
C2 - 26929336
AN - SCOPUS:84962254286
VL - 113
SP - 3287
EP - 3292
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
SN - 0027-8424
IS - 12
ER -