Curran J A, Quinn J P, Hoey E M, Martin S J, Rima B K
J Gen Virol. 1985 May;66 ( Pt 5):977-85. doi: 10.1099/0022-1317-66-5-977.
cDNA clones of the mumps virus N and P messenger RNAs were isolated from an infected cell cDNA library. The N and P clones selected the two predominant polyadenylated RNAs found in mumps virus-infected cells with mol. wt. of 0.69 X 10(6) and 0.51 X 10(6), respectively. In addition, clones of the P gene hybridized to and selected mRNAs of higher mol. wt. probably representing polycistronic transcripts of the mumps genome. Hybrid-select translation experiments confirmed the specificity of the clones as representing the nucleocapsid (N) and nucleocapsid-associated protein (P) genes.
从受感染细胞的cDNA文库中分离出腮腺炎病毒N和P信使RNA的cDNA克隆。所选择的N和P克隆确定了在腮腺炎病毒感染细胞中发现的两种主要的多聚腺苷酸化RNA,其分子量分别为0.69×10⁶和0.51×10⁶。此外,P基因的克隆与分子量更高的mRNA杂交并进行了选择,这些mRNA可能代表腮腺炎病毒基因组的多顺反子转录本。杂交选择翻译实验证实了这些克隆作为代表核衣壳(N)和核衣壳相关蛋白(P)基因的特异性。