scispace - formally typeset
Open AccessJournal ArticleDOI

Polo-like kinases: a team that plays throughout mitosis

David M. Glover, +2 more
- 15 Dec 1998 - 
- Vol. 12, Iss: 24, pp 3777-3787
Reads0
Chats0
TLDR
The current status of the understanding of the functions of plks is reviewed from the time of commitment to M phase in the activation of Cdc25, through theactivation of the anaphase promoting complex (APC), to the regulation of late mitotic events essential for cytokinesis.
Abstract
When the first mutant allele of the Drosophila genepolo was first characterized over 10 years ago, attention focused on the defects that centrosome behavior exhibited at various stages of development (Sunkel and Glover 1988). The subsequent realization that the serine-threonine kinase it encodes is highly conserved from yeasts to humans has provoked a flurry of investigation into the function of the enzyme. A role for the polo-like kinases (plks) in regulating centrosome behavior has been borne out in several organisms, and the enzymes have attracted further attention recently with the realization that they regulate multiple stages of mitotic progression. In this article we review the current status of our understanding of the functions of plks from the time of commitment to M phase in the activation of Cdc25, through the activation of the anaphase promoting complex (APC), to the regulation of late mitotic events essential for cytokinesis. We discuss how to reconcile the sometimes apparently disparate observations made upon plk function in different organisms.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Mitotic kinases as regulators of cell division and its checkpoints

TL;DR: An overview of the many mitotic kinases that regulate cell division and the fidelity of chromosome transmission is given.
Journal ArticleDOI

Targeting polo-like kinase 1 for cancer therapy

TL;DR: The structural features of the kinase domain and the unique polo-box domain ofPLK1 that are most suited for drug development are addressed and the current understanding of the therapeutic potential of PLK1 is discussed.
Journal ArticleDOI

The molecular basis for phosphodependent substrate targeting and regulation of Plks by the Polo-box domain.

TL;DR: Mutations that specifically disrupt phosphodependent interactions abolish cell-cycle-dependent localization and provide compelling phenotypic evidence that PBD-phospholigand binding is necessary for proper mitotic progression.
Journal ArticleDOI

Proteomic Screen Finds pSer/pThr-Binding Domain Localizing Plk1 to Mitotic Substrates

TL;DR: This finding reveals how Plk1 can localize to specific sites within cells in response to Cdk phosphorylation at those sites and provides a structural mechanism for targeting the PlK1 kinase domain to its substrates.
Journal ArticleDOI

Molecular Interaction Map of the Mammalian Cell Cycle Control and DNA Repair Systems

TL;DR: The map shows how multiprotein complexes could assemble and function at gene promoter sites and at sites of DNA damage and portrays the richness of connections between the p53-Mdm2 subsystem and other parts of the network.
References
More filters
Journal ArticleDOI

Universal control mechanism regulating onset of M-phase

TL;DR: The onset of M-phase is regulated by a mechanism common to all eukaryotic cells and requires p34cdc2 dephosphorylation and association with cyclin.
Journal ArticleDOI

Mutations of mitotic checkpoint genes in human cancers

TL;DR: It is shown that CIN is consistently associated with the loss of function of a mitotic checkpoint in cancers displaying CIN, and in some cancersThe loss of this checkpoint wasassociated with the mutational inactivation of a human homologue of the yeast BUB1 gene; BUB 1 controls mitotic checkpoints and chromosome segregation in yeast.
Journal ArticleDOI

Uncoupling of obesity from insulin resistance through a targeted mutation in aP2, the adipocyte fatty acid binding protein.

TL;DR: Results indicate that aP2 is central to the pathway that links obesity to insulin resistance, possibly by linking fatty acid metabolism to expression of TNF-α.
Journal ArticleDOI

Genetic control of the cell division cycle in the fission yeast Schizosaccharomyces pombe

TL;DR: Physiological characterisation of the mutants has shown that DNA synthesis and nuclear division form a cycle of mutually dependent events which can operate in the absence of cell plate formation.
Journal ArticleDOI

Abnormal Centrosome Amplification in the Absence of p53

TL;DR: In mouse embryonic fibroblasts lacking the p53 tumor suppressor protein, multiple copies of functionally competent centrosomes are generated during a single cell cycle, implicate p53 in the regulation of centrosome duplication and suggest one possible mechanism by which the loss of p53 may cause genetic instability.
Related Papers (5)