| Literature DB >> 35775922 |
Guolong Mo1,2, Ruizhen Li1, Zachary Swider3,4, Julie Leblanc1, William M Bement3,4,5, X Johné Liu1,2,6.
Abstract
Polar body emission is a special form of cytokinesis in oocyte meiosis that ensures the correct number of chromosomes in reproduction-competent eggs. The molecular mechanism of the last step, polar body abscission, is poorly understood. While it has been proposed that Ca2+ signaling plays important roles in embryonic cytokinesis, to date transient increases in intracellular free Ca2+ have been difficult to document in oocyte meiosis except for the global Ca2+ wave induced by sperm at fertilization. Here, we find that microinjection of the calcium chelator dibromo-BAPTA inhibits polar body abscission in Xenopus laevis oocytes. Using a novel, microtubule-targeted ratio-metric calcium sensor, we detected a calcium transient that is focused at the contractile ring-associated plasma membrane and which occurred after anaphase and constriction of the contractile ring but prior to abscission. This calcium transient was confirmed by mobile calcium probes. Further, the Ca2+-sensitive protein kinase Cβ C2 domain transiently translocated to the contractile ring-associated membrane simultaneously with the calcium transient. Collectively, these results demonstrate that a calcium transient, apparently originating at the contractile ring-associated plasma membrane, promotes polar body abscission.Entities:
Keywords: Xenopus oocytes; abscission; calcium; meiosis; polar body
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Year: 2022 PMID: 35775922 PMCID: PMC9586590 DOI: 10.1080/15384101.2022.2092815
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 5.173