Green M, Graves P N, Zehavi-Willner T, McInnes J, Pestka S
Proc Natl Acad Sci U S A. 1975 Jan;72(1):224-8. doi: 10.1073/pnas.72.1.224.
Total poly(A)-containing mRNA was isolated from the MOPC-315 and MOPC-315 NR plasmacytomas. The RNA was further fractionated on sodium dodecyl sulfate-sucrose gradients. The MOPC-315 mRNA fractions directed the synthesis of both the heavy chain and light chain precursor of the MOPC-315 IgA protein in a cell-free extract of Ehrlich ascites tumor cells. None of the MOPC-315 NR mRNA fractions tested programmed the synthesis of the heavy chain in this system. Analysis of cell-free products by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and by immunoprecipitation demonstrated that no translatable heavy chain mRNA could be extracted from the MOPC-315 NR variant plasmacytoma.
从MOPC - 315和MOPC - 315 NR浆细胞瘤中分离出总含聚腺苷酸(poly(A))的mRNA。RNA进一步在十二烷基硫酸钠 - 蔗糖梯度上进行分级分离。MOPC - 315 mRNA级分在艾氏腹水瘤细胞的无细胞提取物中指导合成MOPC - 315 IgA蛋白的重链和轻链前体。在该系统中,所测试的MOPC - 315 NR mRNA级分均未编程重链的合成。通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳和免疫沉淀对无细胞产物进行分析表明,无法从MOPC - 315 NR变异浆细胞瘤中提取出可翻译的重链mRNA。