Recent Progress on the Localization of the Spindle Assembly Checkpoint Machinery to Kinetochores

被引:35
作者
Dou, Zhen [1 ]
Prifti, Diogjena Katerina [2 ]
Gui, Ping [1 ,3 ]
Liu, Xing [1 ,3 ]
Elowe, Sabine [2 ,4 ,5 ]
Yao, Xuebiao [1 ,6 ]
机构
[1] Univ Sci & Technol China, Anhui Key Lab Cellular Dynam & Chem Biol, Hefei Natl Sci Ctr Phys Sci Microscale, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
[2] Univ Laval, Fac Med, Programme Mol & Cellular Biol, Bur 4633, 1050 Ave Med, Quebec City, PQ G1V 0A6, Canada
[3] Morehouse Sch Med, Keck Ctr Cellular Dynam & Organoids Plast, Atlanta, GA 30310 USA
[4] Univ Laval, Ctr Rech CHU Quebec, Bur 4633, 1050 Ave Med, Quebec City, PQ G1V 0A6, Canada
[5] Univ Laval, Fac Med, Dept Pediat, Bur 4633, 1050 Ave Med, Quebec City, PQ G1V 0A6, Canada
[6] CAS Ctr Excellence Mol Cell Sci, Hefei 230027, Anhui, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
spindle assembly checkpoint (SAC); kinetochore; microtubule; kinase; localization; CHROMOSOMAL PASSENGER COMPLEX; AURORA-B KINASE; MITOTIC CHECKPOINT; MICROTUBULE ATTACHMENT; OUTER KINETOCHORE; MPS1; KINASE; CENP-E; UNATTACHED KINETOCHORES; PHOSPHO-REGULATION; YEAST KINETOCHORE;
D O I
10.3390/cells8030278
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Faithful chromosome segregation during mitosis is crucial for maintaining genome stability. The spindle assembly checkpoint (SAC) is a surveillance mechanism that ensures accurate mitotic progression. Defective SAC signaling leads to premature sister chromatid separation and aneuploid daughter cells. Mechanistically, the SAC couples the kinetochore microtubule attachment status to the cell cycle progression machinery. In the presence of abnormal kinetochore microtubule attachments, the SAC prevents the metaphase-to-anaphase transition through a complex kinase-phosphatase signaling cascade which results in the correct balance of SAC components recruited to the kinetochore. The correct kinetochore localization of SAC proteins is a prerequisite for robust SAC signaling and, hence, accurate chromosome segregation. Here, we review recent progresses on the kinetochore recruitment of core SAC factors.
引用
收藏
页数:15
相关论文
共 134 条
[11]   Human Zw10 and ROD ave mitotic checkpoint proteins that bind to kinetochores [J].
Chan, GKT ;
Jablonski, SA ;
Starr, DA ;
Goldberg, ML ;
Yen, TJ .
NATURE CELL BIOLOGY, 2000, 2 (12) :944-947
[12]   Molecular architecture of the kinetochore-microtubule interface [J].
Cheeseman, Iain M. ;
Desai, Arshad .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (01) :33-46
[13]   The conserved KMN network constitutes the core microtubule-binding site of the kinetochore [J].
Cheeseman, Iain M. ;
Chappie, Joshua S. ;
Wilson-Kubalek, Elizabeth M. ;
Desai, Arshad .
CELL, 2006, 127 (05) :983-997
[14]   A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension [J].
Cheeseman, IM ;
Niessen, S ;
Anderson, S ;
Hyndman, F ;
Yates, JR ;
Oegema, K ;
Desai, A .
GENES & DEVELOPMENT, 2004, 18 (18) :2255-2268
[15]   Phospho-regulation of kinetochore-microtubule attachments by the aurora kinase Ipl1p [J].
Cheeseman, LM ;
Anderson, S ;
Jwa, M ;
Green, EM ;
Kang, JS ;
Yates, JR ;
Chan, CSM ;
Drubin, DG ;
Barnes, G .
CELL, 2002, 111 (02) :163-172
[16]   Phosphorylation and activation of Bub1 on unattached chromosomes facilitate the spindle checkpoint [J].
Chen, RH .
EMBO JOURNAL, 2004, 23 (15) :3113-3121
[17]   The spindle checkpoint of budding yeast depends on a tight complex between the Mad1 and Mad2 proteins [J].
Chen, RH ;
Brady, DM ;
Smith, D ;
Murray, AW ;
Hardwick, KG .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (08) :2607-2618
[18]   BubR1 is essential for kinetochore localization of other spindle checkpoint proteins and its phosphorylation requires Mad1 [J].
Chen, RH .
JOURNAL OF CELL BIOLOGY, 2002, 158 (03) :487-496
[19]   Implications for kinetochore-microtubule attachment from the structure of an engineered Ndc80 complex [J].
Ciferri, Claudio ;
Pasqualato, Sebastiano ;
Screpanti, Emanuela ;
Varetti, Gianluca ;
Santaguida, Stefano ;
Dos Reis, Gabriel ;
Maiolica, Alessio ;
Polka, Jessica ;
De Luca, Jennifer G. ;
De Wulf, Peter ;
Salek, Mogjiborahman ;
Rappsilber, Juri ;
Moores, Carolyn A. ;
Salmon, Edward D. ;
Musacchio, Andrea .
CELL, 2008, 133 (03) :427-439
[20]   Mps1 Phosphorylates Its N-Terminal Extension to Relieve Autoinhibition and Activate the Spindle Assembly Checkpoint [J].
Combes, Guillaume ;
Barysz, Helena ;
Garand, Chantal ;
Braga, Luciano Gama ;
Alharbi, Ibrahim ;
Thebault, Philippe ;
Murakami, Luc ;
Bryne, Dominic P. ;
Stankovic, Stasa ;
Eyers, Patrick A. ;
Bolanos-Garcia, Victor M. ;
Earnshaw, William C. ;
Maciejowski, John ;
Jallepalli, Prasad V. ;
Elowe, Sabine .
CURRENT BIOLOGY, 2018, 28 (06) :872-+