Ca2+ Oscillations Promote APC/C-Dependent Cyclin B1 Degradation during Metaphase Arrest and Completion of Meiosis in Fertilizing Mouse Eggs

• Published in: Current biology Vol. 12; no. 9; pp. 746 - 750
• Main Authors: Nixon, Victoria L., Levasseur, Mark, McDougall, Alex, Jones, Keith T.
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01.04.2002; Elsevier
• Subjects: Cellular Biology; Life Sciences
• ISSN: 0960-9822; 1879-0445
• DOI: 10.1016/S0960-9822(02)00811-4

Cyclin B1, the regulatory component of M phase-promoting factor (MPF), is degraded during the metaphase-anaphase transition in an anaphase-promoting complex/cyclosome (APC/C)-dependent process [1]. MPF activity is stable in eggs, and a sperm-triggered Ca2+ signal is needed to promote cyclin degradation [2]. In frogs, a single Ca2+ spike promotes cell cycle resumption, but, in mammals, the Ca2+ signal is more complex, consisting of a series of spikes that stop several hours after sperm fusion [3]. Using dual imaging in mouse eggs, we have examined how the Ca2+ signal generates cyclin B1 destruction using destructible and nondestructible GFP-tagged constructs. APC/C activity was present in unfertilized eggs, giving cyclin B1 a half-life of 1.15 ± 0.28 hr. However, APC/C-dependent cyclin degradation was elevated 6-fold when sperm raised cytosolic Ca2+ levels above 600 nM. This activation was transitory since cyclin B1 levels recovered between Ca2+ spikes. For continued cyclin degradation at basal Ca2+ levels, multiple spikes were needed. APC/C-mediated degradation was observed until eggs had completed meiosis with the formation of pronuclei, and, at this time, Ca2+ spikes stopped. Therefore, the physiological need for a repetitive Ca2+ signal in mammals is to ensure long-term cyclin destruction during a protracted exit from meiosis.