γ-Taxilin temporally regulates centrosome disjunction in a Nek2A-dependent manner

Journal Article · Mon Jan 15 04:00:00 EST 2018 · Experimental Cell Research

DOI:https://doi.org/10.1016/J.YEXCR.2017.12.004· OSTI ID:23082490

Makiyama, Tomohiko ^[1]; Higashi, Satoru ^[1]; Sakane, Hiroshi ^[1]; Nogami, Satoru ^[1]; Shirataki, Hiromichi ^[1]

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1. Department of Molecular and Cell Biology, Graduate School of Medicine, Dokkyo Medical University, 880 Kitakobayashi, Mibu-town, Tochigi 321-0293 (Japan)

Highlights: • γ-Taxilin co-localizes with Nek2A at the centrosome during interphase. • γ-Taxilin interacts with Nek2A in yeast two-hybrid and pull-down assays. • γ-Taxilin protein expression levels decrease at the onset of mitosis. • γ-Taxilin depletion induces immature splitting of centrosomes. • The immature splitting of centrosomes induced by γ-taxilin depletion depends on Nek2A. Never in mitosis A-related kinase 2A (Nek2A), a centrosomal serine/threonine kinase, is involved in mitotic progression by regulating the centrosome cycle. Particularly, Nek2A is necessary for dissolution of the intercentriole linkage between the duplicated centrosomes prior to mitosis. Nek2A activity roughly parallels its cell cycle-dependent expression levels, but the precise mechanism regulating its activity remains unclear. In this study, we found that γ-taxilin co-localized with Nek2A at the centrosome during interphase and interacted with Nek2A in yeast two-hybrid and pull-down assays and that γ-taxilin regulated centrosome disjunction in a Nek2A-dependent manner. γ-Taxilin depletion increased the number of cells with striking splitting of centrosomes. The precocious splitting of centrosomes induced by γ-taxilin depletion was attenuated by Nek2A depletion, suggesting that γ-taxilin depletion induces the Nek2A-mediated dissolution of the intercentriole linkage between the duplicated centrosomes nevertheless mitosis does not yet begin. Taken together with the result that γ-taxilin protein expression levels were decreased at the onset of mitosis, we propose that γ-taxilin participates in Nek2A-mediated centrosome disjunction as a negative regulator through its interaction with Nek2A.

• OSTI ID: 23082490
• Journal Information: Experimental Cell Research, Journal Name: Experimental Cell Research Journal Issue: 2 Vol. 362; ISSN 0014-4827; ISSN ECREAL
• Country of Publication: United States
• Language: English

Related Subjects

60 APPLIED LIFE SCIENCES
CELL CYCLE
MITOSIS
PHOSPHOTRANSFERASES
SERINE
THREONINE
YEASTS