Ho Y, Doherty A S, Schultz R M
Department of Biology, University of Pennsylvania, Philadelphia 19104-6018.
Mol Reprod Dev. 1994 Jun;38(2):131-41. doi: 10.1002/mrd.1080380203.
Results of previous studies indicate that culture of preimplantation mouse embryos in SOM medium containing 85 mM NaCl promotes better development in vitro, as well as supporting higher rates of protein synthesis, when compared to culture in SOM containing 125 mM NaCl (Anbari and Schultz, 1993, Mol Reprod Dev 35:24-28; Biggers et al., 1993, Mol Reprod Dev 34:380-390). In the present study we compare the effect of culturing embryos in these 2 media on several aspects of RNA synthesis and gene expression in order to determine whether the reduced development in SOM containing 125 mM NaCl and lower rates of protein synthesis are correlated with decreases in RNA synthesis and stability and changes in gene expression. Although no apparent differences in the metabolism of [3H]uridine to UMP, UDP, and UTP and its incorporation into total RNA are observed when 2-cell embryos are cultured to the morula stage in either medium, a 20% decrease in the rate of mRNA synthesis is found when embryos are cultured in SOM containing 125 mM NaCl. In addition, pulse-chase experiments reveal that total mRNA is less stable when the embryos are cultured in SOM containing 125 mM NaCl. Using a reverse transcription-polymerase chain reaction to assay for changes in the relative amounts of specific mRNAs, the relative amounts of mRNAs for IGF-I and IGF-II and their cognate receptors are dramatically reduced in embryos cultured in SOM containing 125 mM NaCl, whereas only a mild reduction is observed in the relative amount of actin mRNA. In contrast, when freshly isolated morulae are cultured to the blastocyst stage in either of these 2 media, similar amounts of these mRNAs are observed. Last, high-resolution, 2-dimensional gel electrophoresis reveals significant changes in the pattern of protein synthesis when the embryos are cultured in SOM containing 125 mM NaCl. Results of these experiments suggest that culture of embryos in medium containing lower concentrations of NaCl that are normally present in various culture media results in higher rates of mRNA synthesis and greater mRNA stability. These changes in RNA synthesis may underlie, at least in part, the improved development in vitro that is fostered by SOM containing 85 mM NaCl.
先前研究的结果表明,与在含有125 mM NaCl的SOM培养基中培养相比,将植入前小鼠胚胎在含有85 mM NaCl的SOM培养基中培养可促进更好的体外发育,并支持更高的蛋白质合成速率(安巴里和舒尔茨,1993年,《分子生殖与发育》35:24 - 28;比格斯等人,1993年,《分子生殖与发育》34:380 - 390)。在本研究中,我们比较了在这两种培养基中培养胚胎对RNA合成和基因表达几个方面的影响,以确定在含有125 mM NaCl的SOM中发育减少以及蛋白质合成速率降低是否与RNA合成和稳定性的降低以及基因表达的变化相关。尽管当将2 - 细胞胚胎在任一种培养基中培养至桑椹胚阶段时,未观察到[3H]尿苷代谢为UMP、UDP和UTP及其掺入总RNA的代谢有明显差异,但当胚胎在含有125 mM NaCl的SOM中培养时,发现mRNA合成速率降低了20%。此外,脉冲追踪实验表明,当胚胎在含有125 mM NaCl的SOM中培养时,总mRNA的稳定性较低。使用逆转录 - 聚合酶链反应来检测特定mRNA相对量的变化,在含有125 mM NaCl的SOM中培养的胚胎中,IGF - I和IGF - II及其同源受体的mRNA相对量显著降低,而肌动蛋白mRNA的相对量仅轻微降低。相反,当将新鲜分离的桑椹胚在这两种培养基中的任一种中培养至囊胚阶段时,观察到这些mRNA的量相似。最后,高分辨率二维凝胶电泳显示,当胚胎在含有125 mM NaCl的SOM中培养时,蛋白质合成模式有显著变化。这些实验结果表明,在含有通常存在于各种培养基中较低浓度NaCl的培养基中培养胚胎会导致更高的mRNA合成速率和更高的mRNA稳定性。RNA合成的这些变化可能至少部分地是由含有85 mM NaCl的SOM所促进的体外发育改善的基础。