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Species-Specific Differences in the Activity and Nuclear Localization of Murine and Bovine Phospholipase C Zeta 1

机译:小鼠和牛磷脂酶C Zeta 1的活性和核定位的物种特异性差异。

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摘要

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 ([Ca2+]i), 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 [Ca2+]i 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 [Ca2+]i oscillations at 10-fold lower concentrations than bovine PLCZ1, although in bovine oocytes bovine PLCZ1 was more effective than murine Plcz1 at inducing [Ca2+]i oscillations. Investigation of ITPR1 (IP3R1) 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.
机译:已显示,注射哺乳动物精子提取物或精子特异性磷脂酶C zeta 1(PLCZ1)的cRNA会触发游离钙([Ca 2 + ] i)浓度的重复振荡,从而导致迄今为止研究的所有哺乳动物的卵母细胞活化和胚胎发育。尽管PLCZ1具有跨物种的活性,但还观察到,在将PLCZ1 cRNA注入不同卵母细胞后,[Ca 2 + ] i振荡的频率和模式可能存在物种特异性差异。种类。因此,我们使用交叉设计策略直接研究鼠和牛卵母细胞中鼠和牛PLCZ1的活性。在鼠卵母细胞中,注射鼠Plcz1 cRNA诱导的[Ca 2 + ] i振荡的浓度比牛PLCZ1低10倍,尽管在牛卵母细胞中牛PLCZ1比鼠Plcz1更有效地诱导[Ca 2 + ] i振荡。研究PLCZ1 cRNA在牛卵母细胞中ITPR1(IP3R1)的下调也显示,牛PLCZ1在同源卵母细胞中更具活性。为了确定这些PLCZ是否表现出相似的细胞分布,将金星标记的PLCZ1 cRNA注入卵母细胞,并过表达PLCZ1。尽管具有假定的核定位信号,但牛PLCZ1未能在牛或鼠合子的原核(PN)中积累。相反,鼠PLCZ1累积在鼠和牛合子的PN中。这些结果表明,鼠类PLCZ1和牛PLCZ1在活性上具有物种特异性差异,并表明这两种物种之间蛋白质的作用方式存在潜在差异。物种之间精子PLCZ1蛋白含量的变化,以及卵母细胞特异性的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。

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