CYK-4 functions independently of its centralspindlin partner ZEN-4 to cellularize oocytes in germline syncytia

Kian-Yong Lee 1, 2 Rebecca A Green 1, 2 Edgar Gutierrez 3 J Sebastian Gomez-Cavazos 1, 2 Irina Kolotuev 4 Shaohe Wang 1, 2 Arshad Desai 1, 2 Alex Groisman 3 Karen Oegema 1, 2
1 Ludwig Institute for Cancer Research
2 CMM - Department of Cellular and Molecular Medicine
3 UC San Diego - University of California [San Diego]
4 MRic - Centre de Microscopie de Rennes
Abstract : Throughout metazoans, germ cells undergo incomplete cytokinesis to form syncytia connected by intercellular bridges. Gamete formation ultimately requires bridge closure, yet how bridges are reactivated to close is not known. The most conserved bridge component is centralspindlin, a complex of the Rho family GTPase-activating protein (GAP) CYK-4/MgcRacGAP and the microtubule motor ZEN-4/kinesin-6. Here, we show that oocyte production by the syncytial Caenorhabditis elegans germline requires CYK-4 but not ZEN-4, which contrasts with cytokinesis, where both are essential. Longitudinal imaging after conditional inactivation revealed that CYK-4 activity is important for oocyte cellularization, but not for the cytokinesis-like events that generate syncytial compartments. CYK-4's lipid-binding C1 domain and the GTPase-binding interface of its GAP domain were both required to target CYK-4 to intercellular bridges and to cellularize oocytes. These results suggest that the conserved C1-GAP region of CYK-4 constitutes a targeting module required for closure of intercellular bridges in germline syncytia.
Keywords : C. elegans Kinesin-6 MgcRacGAP cell biology centralspindlin ring canal intercellular bridge germline syncytia
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Kian-Yong Lee, Rebecca A Green, Edgar Gutierrez, J Sebastian Gomez-Cavazos, Irina Kolotuev, et al.. CYK-4 functions independently of its centralspindlin partner ZEN-4 to cellularize oocytes in germline syncytia. eLife, eLife Sciences Publication, 2018, 7, pp.e36919. ⟨10.7554/eLife.36919⟩. ⟨hal-01862598⟩

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