Plk5, a Polo Box Domain-Only Protein with Specific Roles in Neuron Differentiation and Glioblastoma Suppression

Author:

de Cárcer Guillermo1,Escobar Beatriz1,Higuero Alonso M.2,García Laura1,Ansón Alejandra1,Pérez Gema3,Mollejo Manuela3,Manning Gerard4,Meléndez Bárbara3,Abad-Rodríguez José2,Malumbres Marcos1

Affiliation:

1. Cell Division and Cancer Group, Centro Nacional de Investigaciones Oncológicas, Madrid, Spain

2. Membrane Biology and Axonal Repair Laboratory, Hospital Nacional de Parapléjicos, Toledo, Spain

3. Unidad de Investigación de Patología Molecular, Hospital Virgen de la Salud, Toledo, Spain

4. Razavi Newman Center for Bioinformatics, Salk Institute, La Jolla, California

Abstract

ABSTRACT Polo-like kinases (Plks) are characterized by the presence of a specific domain, known as the polo box (PBD), involved in protein-protein interactions. Plk1 to Plk4 are involved in centrosome biology as well as the regulation of mitosis, cytokinesis, and cell cycle checkpoints in response to genotoxic stress. We have analyzed here the new member of the vertebrate family, Plk5, a protein that lacks the kinase domain in humans. Plk5 does not seem to have a role in cell cycle progression; in fact, it is downregulated in proliferating cells and accumulates in quiescent cells. This protein is mostly expressed in the brain of both mice and humans, and it modulates the formation of neuritic processes upon stimulation of the brain-derived neurotrophic factor (BDNF)/nerve growth factor (NGF)-Ras pathway in neurons. The human PLK5 gene is significantly silenced in astrocytoma and glioblastoma multiforme by promoter hypermethylation, suggesting a tumor suppressor function for this gene. Indeed, overexpression of Plk5 has potent apoptotic effects in these tumor cells. Thus, Plk5 seems to have evolved as a kinase-deficient PBD-containing protein with nervous system-specific functions and tumor suppressor activity in brain cancer.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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