Endres M J, Jacoby D R, Janssen R S, Gonzalez-Scarano F, Nathanson N
Department of Microbiology, School of Medicine, University of Pennsylvania, Philadelphia 19104.
J Gen Virol. 1989 Jan;70 ( Pt 1):223-8. doi: 10.1099/0022-1317-70-1-223.
Reassortant bunyaviruses derived from two members of the California serogroup (La Crosse/original and Tahyna/181-57) viruses were used to demonstrate that the large Mr viral protein (L) is encoded by the L RNA segment. Radiolabelled viral proteins were analysed by discontinuous SDS-PAGE. The L protein of La Crosse virus was observed to migrate ahead of its Tahyna virus counterpart when electrophoresed through a 5% acrylamide resolving gel. Among the reassortant viruses, the L protein phenotype segregated with the viral L RNA segment. After confirming the genotype of the viruses used in this study, it was concluded that the L RNA species of California serogroup viruses codes for the L protein, the presumed viral polymerase.
源自加利福尼亚血清群的两个成员(拉克罗斯病毒/原始毒株和塔希纳病毒/181 - 57)的重配布尼亚病毒被用于证明病毒大分子量蛋白(L)由L RNA片段编码。通过不连续SDS - PAGE分析放射性标记的病毒蛋白。当通过5%丙烯酰胺分离凝胶进行电泳时,观察到拉克罗斯病毒的L蛋白比其塔希纳病毒对应物迁移得更快。在重配病毒中,L蛋白表型与病毒L RNA片段分离。在确认本研究中使用的病毒基因型后,得出结论:加利福尼亚血清群病毒的L RNA种类编码L蛋白,即推测的病毒聚合酶。