PLCζ is the physiological trigger of the Ca2+ oscillations that induce embryogenesis in mammals but conception can occur in its absence

Activation of the egg by the sperm is the first, vital stage of embryogenesis. The sperm protein PLC zeta has been proposed as the physiological agent that triggers the Ca2+ oscillations that normally initiate embryogenesis. Consistent with this, recombinant PLC zeta induces Ca2+ oscillations in eggs and debilitating mutations in the PLCZ1 gene are associated with infertility in men. However, there has been no evidence that knockout of the gene encoding PLC. abolishes the ability of sperm to induce Ca2+ oscillations in eggs. Here, we show that sperm derived from Plcz1(-/-) male mice fail to trigger Ca2+ oscillations in eggs, cause polyspermy and thus demonstrate that PLC zeta is the physiological trigger of these Ca2+ oscillations. Remarkably, some eggs fertilized by PLC zeta-null sperm can develop, albeit at greatly reduced efficiency, and after a significant time-delay. In addition, Plcz1(-/-) males are subfertile but not sterile, suggesting that in the absence of PLC zeta, spontaneous egg activation can eventually occur via an alternative route. This is the first demonstration that in vivo fertilization without the normal physiological trigger of egg activation can result in offspring. PLC zeta-null sperm now make it possible to resolve long-standing questions in fertilization biology, and to test the efficacy and safety of procedures used to treat human infertility.Activation of the egg by the sperm is the first, vital stage of embryogenesis. The sperm protein PLC zeta has been proposed as the physiological agent that triggers the Ca2+ oscillations that normally initiate embryogenesis. Consistent with this, recombinant PLC zeta induces Ca2+ oscillations in eggs and debilitating mutations in the PLCZ1 gene are associated with infertility in men. However, there has been no evidence that knockout of the gene encoding PLC. abolishes the ability of sperm to induce Ca2+ oscillations in eggs. Here, we show that sperm derived from Plcz1(-/-) male mice fail to trigger Ca2+ oscillations in eggs, cause polyspermy and thus demonstrate that PLC zeta is the physiological trigger of these Ca2+ oscillations. Remarkably, some eggs fertilized by PLC zeta-null sperm can develop, albeit at greatly reduced efficiency, and after a significant time-delay. In addition, Plcz1(-/-) males are subfertile but not sterile, suggesting that in the absence of PLC zeta, spontaneous egg activation can eventually occur via an alternative route. This is the first demonstration that in vivo fertilization without the normal physiological trigger of egg activation can result in offspring. PLC zeta-null sperm now make it possible to resolve long-standing questions in fertilization biology, and to test the efficacy and safety of procedures used to treat human infertility.A