Motor activity of centromere-associated protein-E contributes to its localization at the center of the midbody to regulate cytokinetic abscission

被引:10
作者
Ohashi, Akihiro [1 ]
Ohori, Momoko [1 ]
Iwai, Kenichi [1 ]
机构
[1] Takeda Pharmaceut Co Ltd, Div Pharmaceut Res, Oncol Drug Discovery Unit, Osaka, Japan
关键词
CENP-E; cytokinetic abscission; midbody localization; PRC1; CENP-E inhibitor; MICROTUBULE CROSS-LINKING; CENP-E; CENTRAL SPINDLE; CHROMOSOME ALIGNMENT; KINETOCHORE PROTEIN; MITOTIC CHECKPOINT; MIDZONE FORMATION; DNA-DAMAGE; AURORA B; PRC1;
D O I
10.18632/oncotarget.13206
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accurate control of cytokinesis is critical for genomic stability to complete high-fidelity transmission of genetic material to the next generation. A number of proteins accumulate in the intercellular bridge (midbody) during cytokinesis, and the dynamics of these proteins are temporally and spatially orchestrated to complete the process. In this study, we demonstrated that localization of centromere-associated protein-E (CENP-E) at the midbody is involved in cytokinetic abscission. The motor activity of CENP-E and the C-terminal midbody localization domain, which includes amino acids 2659-2666 (RYFDNSSL), are involved in the anchoring of CENP-E to the center of the midbody. Furthermore, CENP-E motor activity contributes to the accumulation of protein regulator of cytokinesis 1 (PRC1) in the midbody during cytokinesis. Midbody localization of PRC1 is critical to the antiparallel microtubule structure and recruitment of other midbody-associated proteins. Therefore, CENP-E motor activity appears to play important roles in the organization of these proteins to complete cytokinetic abscission. Our findings will be helpful for understanding how each step of cytokinesis is regulated to complete cytokinetic abscission.
引用
收藏
页码:79964 / 79980
页数:17
相关论文
共 44 条
  • [1] Microtubule detyrosination guides chromosomes during mitosis
    Barisic, Marin
    Silva e Sousa, Ricardo
    Tripathy, Suvranta K.
    Magiera, Maria M.
    Zaytsev, Anatoly V.
    Pereira, Ana L.
    Janke, Carsten
    Grishchuk, Ekaterina L.
    Maiato, Helder
    [J]. SCIENCE, 2015, 348 (6236) : 799 - 803
  • [2] KIF4A and PP2A-B56 form a spatially restricted feedback loop opposing Aurora B at the anaphase central spindle
    Bastos, Ricardo Nunes
    Cundell, Michael J.
    Barr, Francis A.
    [J]. JOURNAL OF CELL BIOLOGY, 2014, 207 (06) : 683 - 693
  • [3] Aurora B suppresses microtubule dynamics and limits central spindle size by locally activating KIF4A
    Bastos, Ricardo Nunes
    Gandhi, Sapan R.
    Baron, Ryan D.
    Gruneberg, Ulrike
    Nigg, Erich A.
    Barr, Francis A.
    [J]. JOURNAL OF CELL BIOLOGY, 2013, 202 (04) : 605 - 621
  • [4] A Minimal Midzone Protein Module Controls Formation and Length of Antiparallel Microtubule Overlaps
    Bieling, Peter
    Telley, Ivo A.
    Surrey, Thomas
    [J]. CELL, 2010, 142 (03) : 420 - 432
  • [5] Chromosome congression in the absence of kinetochore fibres
    Cai, Shang
    O'Connell, Christopher B.
    Khodjakov, Alexey
    Walczak, Claire E.
    [J]. NATURE CELL BIOLOGY, 2009, 11 (07) : 832 - U118
  • [6] Incisive Imaging and Computation for Cellular Mysteries: Lessons from Abscission
    Elia, Natalie
    Ott, Carolyn
    Lippincott-Schwartz, Jennifer
    [J]. CELL, 2013, 155 (06) : 1220 - 1231
  • [7] Crystal structure of the motor domain of the human kinetochore protein CENP-E
    Garcia-Saez, I
    Yen, T
    Wade, RH
    Kozielski, F
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (05) : 1107 - 1116
  • [8] The molecular requirements for cytokinesis
    Glotzer, M
    [J]. SCIENCE, 2005, 307 (5716) : 1735 - 1739
  • [9] The 3Ms of central spindle assembly: microtubules, motors and MAPs
    Glotzer, Michael
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (01) : 9 - 20
  • [10] KIF14 and citron kinase act together to promote efficient cytokinesis
    Gruneberg, U
    Neef, R
    Li, XL
    Chan, EHY
    Chalamalasetty, RB
    Nigg, EA
    Barr, FA
    [J]. JOURNAL OF CELL BIOLOGY, 2006, 172 (03) : 363 - 372