Wiggins T L, Tucciarone L M, Lanclos K D
Mol Cell Biochem. 1978 Nov 16;21(3):145-51. doi: 10.1007/BF00240133.
Total Xenopus liver cytoplasmic RNA isolated following long-term estrogen administration (14 days) was fractioned using Sepharose 4B chromatography. One of the Sepharose 4B peaks was shown to contain RNA with a molecular weight reported for vitellogenin mRNA (approximately 34S). The presence of estrogen-induced vitellogenin mRNA in the peak 5 RNA was determined by translation of the RNA in the oocyte and analysis of the oocyte translational products by immunoprecipitation with anti-vitellogenin. Sepharose 4B peaks 2 and 3 were also observed to contain estrogen induced mRNA populations sedimenting between 9--18S. These findings suggest that Sepharose 4B chromatography might prove useful in separating different mRNA populations following estrogen-induced gene activation.
长期给予雌激素(14天)后分离得到的非洲爪蟾肝脏细胞质总RNA,使用琼脂糖4B层析法进行分级分离。琼脂糖4B层析的一个峰显示含有分子量与卵黄蛋白原mRNA报道值(约34S)相符的RNA。通过在卵母细胞中翻译该RNA并用抗卵黄蛋白原进行免疫沉淀分析卵母细胞翻译产物,确定了峰5 RNA中存在雌激素诱导的卵黄蛋白原mRNA。还观察到琼脂糖4B层析的峰2和峰3含有沉降系数在9 - 18S之间的雌激素诱导的mRNA群体。这些发现表明,琼脂糖4B层析可能在分离雌激素诱导的基因激活后的不同mRNA群体方面很有用。