Polo-like kinase 1 promotes Cdc42-induced actin polymerization for asymmetric division in oocytes. Issue 3 (8th March 2023)

• Record Type: Journal Article
• Authors: Yuen, Wai Shan; Zhang, Qing Hua; Bourdais, Anne; Adhikari, Deepak; Halet, Guillaume; Carroll, John
• Is Part Of: Open biology. Volume 13:Issue 3(2023)
• Publication Date: 2023-03-08
• Subjects: Plk1 -- Cdc42 -- actin -- meiosis -- oocyte -- polarity; Biology -- Periodicals; 570
• DOI: 10.1098/rsob.220326
• Languages: English
• ISSNs: 2046-2441

Abstract

Abstract : Abstract : Polo-like kinase I (Plk1) is a highly conserved seronine/threonine kinase essential in meiosis and mitosis for spindle formation and cytokinesis. Here, through temporal application of Plk1 inhibitors, we identify a new role for Plk1 in the establishment of cortical polarity essential for highly asymmetric cell divisions of oocyte meiosis. Application of Plk1 inhibitors in late metaphase I abolishes pPlk1 from spindle poles and prevents the induction of actin polymerization at the cortex through inhibition of local recruitment of Cdc42 and Neuronal Wiskott-Aldrich Syndrome protein (N-WASP). By contrast, an already established polar actin cortex is insensitive to Plk1 inhibitors, but if the polar cortex is first depolymerized, Plk1 inhibitors completely prevent its restoration. Thus, Plk1 is essential for establishment but not maintenance of cortical actin polarity. These findings indicate that Plk1 regulates recruitment of Cdc42 and N-Wasp to coordinate cortical polarity and asymmetric cell division.