Kalland K H, Endresen C, Haukenes G
Department of Microbiology and Immunology, Gade Institute, Bergen, Norway.
APMIS. 1988 Mar;96(3):265-72. doi: 10.1111/j.1699-0463.1988.tb05300.x.
Several cDNA libraries have been generated from poly(A)RNA from Vero cells infected for 24 hours with measles virus. Different protocols for cDNA library construction were compared and some critical steps were evaluated. From these libraries, a measles virus specific sequence corresponding to 885 of 1600 nucleotides of the measles virus phosphoprotein gene has been cloned. The phosphoprotein gene accounts for 1% of the total cDNA library after 24 hours of infection at 37 degrees C. The technique of differential colony hybridization was used to analyze the distribution and change of the poly(A)-RNA expression in uninfected Vero cells and in cells infected with measles virus for 24 hours.
已经从感染麻疹病毒24小时的Vero细胞的聚腺苷酸RNA中构建了几个cDNA文库。比较了构建cDNA文库的不同方案,并评估了一些关键步骤。从这些文库中,克隆到了与麻疹病毒磷蛋白基因1600个核苷酸中885个核苷酸相对应的麻疹病毒特异性序列。在37℃感染24小时后,磷蛋白基因占总cDNA文库的1%。采用差异菌落杂交技术分析了未感染的Vero细胞和感染麻疹病毒24小时的细胞中聚腺苷酸RNA表达的分布和变化。