NIMA-related kinase 1 (NEK1) regulates meiosis I spindle assembly by altering the balance between α-Adducin and Myosin X

被引:16
作者
Brieno-Enriquez, Miguel A. [1 ]
Moak, Stefannie L.
Holloway, J. Kim
Cohen, Paula E.
机构
[1] Cornell Univ, Dept Biomed Sci, Ithaca, NY 14850 USA
关键词
POLYCYSTIC KIDNEY-DISEASE; CALMODULIN-BINDING DOMAIN; SEXUAL-DIMORPHISM; CHROMOSOME SEGREGATION; MICROTUBULE-BINDING; MAMMALIAN MEIOSIS; PROTEIN-KINASE; GERM-CELLS; CENTROSOME; PHOSPHORYLATION;
D O I
10.1371/journal.pone.0185780
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
NIMA-related kinase 1 (NEK1) is a serine/threonine and tyrosine kinase that is highly expressed in mammalian germ cells. Mutations in Nek1 induce anemia, polycystic kidney and infertility. In this study we evaluated the role of NEK1 in meiotic spindle formation in both male and female gametes. Our results show that the lack of NEK1 provokes an abnormal organization of the meiosis I spindle characterized by elongated and/or multipolar spindles, and abnormal chromosome congression. The aberrant spindle structure is concomitant with the disruption in localization and protein levels of myosin X (MYO10) and alpha-adducin (ADD1), both of which are implicated in the regulation of spindle formation during mitosis. Interaction of ADD1 with MYO10 is dependent on phosphorylation, whereby phosphorylation of ADD1 enables its binding to MYO10 on mitotic spindles. Reduction in ADD1 protein in NEK1 mutant mice is associated with hyperphosphorylation of ADD1, thereby preventing the interaction with MYO10 during meiotic spindle formation. Our results reveal a novel regulatory role for NEK1 in the regulation of spindle architecture and function during meiosis.
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页数:18
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