Polo-like kinases: structural variations lead to multiple functions

被引:376
作者
Zitouni, Sihem [1 ]
Nabais, Catarina [1 ]
Jana, Swadhin Chandra [1 ]
Guerrero, Adan [1 ]
Bettencourt-Dias, Monica [1 ]
机构
[1] Inst Gulbenkian Ciencias, P-2780156 Oeiras, Portugal
基金
欧洲研究理事会;
关键词
CELL-CYCLE ARREST; REGULATES CENTRIOLE DUPLICATION; SPINDLE-ASSEMBLY CHECKPOINT; PROTEIN PHOSPHATASE 2A; C.-ELEGANS; CENTROSOME DUPLICATION; PLK1; PHOSPHORYLATION; DNA-DAMAGE; AURORA-A; TUMOR-SUPPRESSOR;
D O I
10.1038/nrm3819
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Members of the polo-like kinase (PLK) family are crucial regulators of cell cycle progression, centriole duplication, mitosis, cytokinesis and the DNA damage response. PLKs undergo major changes in abundance, activity, localization and structure at different stages of the cell cycle. They interact with other proteins in a tightly controlled spatiotemporal manner as part of a network that coordinates key cell cycle events. Their essential roles are highlighted by the fact that alterations in PLK function are associated with cancers and other diseases. Recent knowledge gained from PLK crystal structures, evolution and interacting molecules offers important insights into the mechanisms that underlie their regulation and activity, and suggests novel functions unrelated to cell cycle control for this family of kinases.
引用
收藏
页码:433 / 452
页数:20
相关论文
共 208 条
[41]   Asterless is a scaffold for the onset of centriole assembly [J].
Dzhindzhev, Nikola S. ;
Yu, Quan D. ;
Weiskopf, Kipp ;
Tzolovsky, George ;
Cunha-Ferreira, Ines ;
Riparbelli, Maria ;
Rodrigues-Martins, Ana ;
Bettencourt-Dias, Monica ;
Callaini, Giuliano ;
Glover, David M. .
NATURE, 2010, 467 (7316) :714-U104
[42]   Polo-like kinases and oncogenesis [J].
Eckerdt, F ;
Yuan, JP ;
Strebhardt, K .
ONCOGENE, 2005, 24 (02) :267-276
[43]   Identification of a Polo-like Kinase 4-Dependent Pathway for De Novo Centriole Formation [J].
Eckerdt, Frank ;
Yamamoto, Tomomi M. ;
Lewellyn, Andrea L. ;
Maller, James L. .
CURRENT BIOLOGY, 2011, 21 (05) :428-432
[44]   The molecular basis for phosphodependent substrate targeting and regulation of Plks by the Polo-box domain [J].
Elia, AEH ;
Rellos, P ;
Haire, LF ;
Chao, JW ;
Ivins, FJ ;
Hoepker, K ;
Mohammad, D ;
Cantley, LC ;
Smerdon, SJ ;
Yaffe, MB .
CELL, 2003, 115 (01) :83-95
[45]   Proteomic screen finds pSer/pThr-binding domain localizing Plk1 to mitotic substrates [J].
Elia, AEH ;
Cantley, LC ;
Yaffe, MB .
SCIENCE, 2003, 299 (5610) :1228-1231
[46]   Ste20-like kinase (SLK), a regulatory kinase for polo-like kinase (Plk) during the G2/M transition in somatic cells [J].
Ellinger-Ziegelbauer, H ;
Karasuyama, H ;
Yamada, E ;
Tsujikawa, K ;
Todokoro, K ;
Nishida, E .
GENES TO CELLS, 2000, 5 (06) :491-498
[47]   Tension-sensitive Plk1 phosphorylation on BubR1 regulates the stability of kinetochore-microtubule interactions [J].
Elowe, Sabine ;
Huemmer, Stefan ;
Uldschmid, Andreas ;
Li, Xiuling ;
Nigg, Erich A. .
GENES & DEVELOPMENT, 2007, 21 (17) :2205-2219
[48]   Polo-like kinase 4 transcription is activated via CRE and NRF1 elements, repressed by DREAM through CDE/CHR sites and deregulated by HPV E7 protein [J].
Fischer, Martin ;
Quaas, Marianne ;
Wintsche, Axel ;
Mueller, Gerd A. ;
Engeland, Kurt .
NUCLEIC ACIDS RESEARCH, 2014, 42 (01) :163-180
[49]   Formation of stable attachments between kinetochores and microtubules depends on the B56-PP2A phosphatase [J].
Foley, Emily A. ;
Maldonado, Maria ;
Kapoor, Tarun M. .
NATURE CELL BIOLOGY, 2011, 13 (10) :1265-U216
[50]   CDK11p58 Is Required for Centriole Duplication and Plk4 Recruitment to Mitotic Centrosomes [J].
Franck, Nathalie ;
Montembault, Emilie ;
Rome, Pierre ;
Pascal, Aude ;
Cremet, Jean-Yves ;
Giet, Regis .
PLOS ONE, 2011, 6 (01)