TY - JOUR
T1 - Nek7 kinase accelerates microtubule dynamic instability
AU - Cohen, Sivan
AU - Aizer, Adva
AU - Shav-Tal, Yaron
AU - Yanai, Amiel
AU - Motro, Benny
N1 - Funding Information:
We thank Kathryn T. Applegate and Gaudenz Danuser from Harvard University for making the PlusTipTracker software package available to the scientific community, and to Sebastien Besson from Danuser's lab for advice. We thank Niels Galjart from Erasmus Medical Center, Rotterdam, for providing the EB3-GFP construct. We thank Joan Roig, IRB Barcelona, for critical reading of the manuscript. This research was supported by the Israel Science Foundation (grant no. 768/11 to BM).
PY - 2013/5
Y1 - 2013/5
N2 - 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.
AB - 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.
KW - Gene targeting
KW - Microtubule dynamics
KW - NIMA kinase
KW - Nek7
KW - SiRNA
UR - http://www.scopus.com/inward/record.url?scp=84874547670&partnerID=8YFLogxK
U2 - 10.1016/j.bbamcr.2012.12.021
DO - 10.1016/j.bbamcr.2012.12.021
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C2 - 23313050
AN - SCOPUS:84874547670
SN - 0167-4889
VL - 1833
SP - 1104
EP - 1113
JO - Biochimica et Biophysica Acta - Molecular Cell Research
JF - Biochimica et Biophysica Acta - Molecular Cell Research
IS - 5
ER -