Nek7 kinase accelerates microtubule dynamic instability

被引:28
作者
Cohen, Sivan [1 ]
Aizer, Adva [1 ]
Shav-Tal, Yaron [1 ]
Yanai, Amiel [1 ]
Motro, Benny [1 ]
机构
[1] Bar Ilan Univ, Mina & Everard Goodman Fac Life Sci, IL-52900 Ramat Gan, Israel
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2013年 / 1833卷 / 05期
基金
以色列科学基金会;
关键词
NIMA kinase; Nek7; Microtubule dynamics; siRNA; Gene targeting; NIMA-FAMILY KINASE; MITOTIC SPINDLE FORMATION; PROTEIN-KINASE; BINDING PROTEIN; CELL; CANCER; EXPRESSION; MITOSIS; GROWTH; END;
D O I
10.1016/j.bbamcr.2012.12.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The NIMA-related kinases (NRK or Nek) are emerging as conserved and crucial regulators of mitosis and cilia formation. The microtubule (MT) network has long been suspected as a major target of the Neks. However, the underlying mechanism remains unclear. Using the PlusTipTracker software, recently developed by the Danuser group, we followed the consequences of alterations in Nek7 levels on MT dynamic instability. siRNA-mediated downregulation of Nek7 in HeLa cells resulted in lower speeds of MT growth and catastrophe, reduction of the relative time spent in catastrophe, and considerably lowered the overall MT dynamicity. Co-expression of Nek7 with the siRNA treatment rescued the MT phenotypes, while ectopic overexpression of Nek7 yielded inverse characteristics compared to Nek7 downregulation. MT dynamics in mouse embryonic fibroblasts derived from targeted null mutants for Nek7 recapitulated the siRNA downregulation phenotypes. Precise MT dynamic instability is critical for accurate shaping of the mitotic spindle and for cilium formation, and higher MT dynamicity is associated with tumorigenicity. Thus, our results can supply a mechanistic explanation for Nek involvement in these processes. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1104 / 1113
页数:10
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