Graber H U, Stettler M, Zurbriggen A
Institut für Tierneurologie, Universität Bern.
Schweiz Arch Tierheilkd. 1996;138(2):99-103.
In the present work an adapted method of the reverse transcriptase polymerase chain reaction (RT-PCR) is described. This procedure was an important tool for cloning a variety of gene sequences derived from oligodendrocytes and canine distemper virus (CDV). Among other applications, the obtained clones were used to produce probes for in situ hybridization and to sequence the inserted DNAs. Due to these molecularbiological techniques new insights were gained into the pathogenesis of CDV-induced demyelination and CDV-persistence in the central nervous system.
在本研究中,描述了一种改进的逆转录聚合酶链反应(RT-PCR)方法。该程序是克隆源自少突胶质细胞和犬瘟热病毒(CDV)的多种基因序列的重要工具。在其他应用中,获得的克隆用于制备原位杂交探针和对插入的DNA进行测序。由于这些分子生物学技术,人们对CDV诱导的脱髓鞘病变的发病机制以及CDV在中枢神经系统中的持续存在有了新的认识。