Centre for Reproduction and Development, Monash Institute of Medical Research, Monash University, Clayton, Victoria, Australia.
Biol Reprod. 2010 Jul;83(1):92-101. doi: 10.1095/biolreprod.109.079814. Epub 2010 Mar 31.
Injection of mammalian sperm extracts or cRNA of the sperm-specific phospholipase C zeta 1 (PLCZ1) has been shown to trigger repetitive oscillations in the concentration of free calcium (Ca(2+)), leading to oocyte activation and embryo development in all mammals studied to date. While PLCZ1 has cross-species activity, it has also been observed that species-specific differences may exist in the frequency and pattern of the resulting Ca(2+) oscillations following PLCZ1 cRNA injection into oocytes of different species. Accordingly, we used a crossover design strategy to directly investigate the activity of murine and bovine PLCZ1 in both murine and bovine oocytes. In murine oocytes, injection of murine Plcz1 cRNA induced Ca(2+) oscillations at 10-fold lower concentrations than bovine PLCZ1, although in bovine oocytes bovine PLCZ1 was more effective than murine Plcz1 at inducing Ca(2+) oscillations. Investigation of ITPR1 (IP(3)R1) down-regulation in bovine oocytes by PLCZ1 cRNA also showed that bovine PLCZ1 was more active in homologous oocytes. To determine whether these PLCZs exhibited similar cellular distribution, Venus-tagged PLCZ1 cRNA was injected into oocytes, and PLCZ1 was overexpressed. Bovine PLCZ1 failed to accumulate in the pronucleus (PN) of bovine or murine zygotes, despite possessing a putative nuclear localization signal. Conversely, murine PLCZ1 accumulated in the PN of both murine and bovine zygotes. These results demonstrate that murine PLCZ1 and bovine PLCZ1 possess species-specific differences in activity and suggest potential differences in the mode of action of the protein between the two species. Variation in sperm PLCZ1 protein content among species, along with oocyte-specific differences in the localization and availability of PLCZ1 substrates, may further contribute to optimize the activation stimulus to enhance embryo development.
向哺乳动物精子提取物或精子特异性磷脂酶 C ζ1 (PLCZ1) 的 cRNA 注射已被证明会引发游离钙浓度(Ca(2+))的重复振荡,从而导致迄今为止研究的所有哺乳动物的卵母细胞激活和胚胎发育。虽然 PLCZ1 具有跨物种活性,但也观察到在不同物种的卵母细胞中注射 PLCZ1 cRNA 后,Ca(2+)振荡的频率和模式可能存在种间差异。因此,我们使用交叉设计策略直接研究了 PLCZ1 在小鼠和牛卵母细胞中的活性。在小鼠卵母细胞中,注射小鼠 Plcz1 cRNA 可诱导 Ca(2+) 振荡,其浓度比牛 PLCZ1 低 10 倍,尽管在牛卵母细胞中,牛 PLCZ1 比小鼠 Plcz1 更有效地诱导 Ca(2+) 振荡。通过 PLCZ1 cRNA 对牛卵母细胞中 ITPR1(IP(3)R1)下调的研究也表明,牛 PLCZ1 在同源卵母细胞中更活跃。为了确定这些 PLCZ 是否表现出相似的细胞分布,将 Venus 标记的 PLCZ1 cRNA 注射到卵母细胞中,过表达 PLCZ1。尽管牛 PLCZ1 具有潜在的核定位信号,但它未能在牛或鼠受精卵的原核 (PN) 中积累。相反,鼠 PLCZ1 在鼠和牛受精卵的 PN 中积累。这些结果表明,鼠 PLCZ1 和牛 PLCZ1 在活性上具有种间差异,并表明该蛋白在两种物种中的作用模式可能存在差异。种间精子 PLCZ1 蛋白含量的变化,以及卵母细胞中 PLCZ1 底物的定位和可用性的差异,可能进一步有助于优化激活刺激以增强胚胎发育。