Baron M D, Shaila M S, Barrett T
AFRC Institute for Animal Health, Pirbright Laboratory, Woking, Surrey, U.K.
J Gen Virol. 1993 Feb;74 ( Pt 2):299-304. doi: 10.1099/0022-1317-74-2-299.
We have cloned several cDNAs derived from the P gene of rinderpest virus. One of these, derived from a bicistronic N-P mRNA, has been sequenced in its entirety. Sequencing of a section of the others, and comparison with the genome sequence, showed that P gene transcripts, as for other morbilliviruses, were variable; non-templated Gs could be added at a site resembling the normal stop transcription site. Primer extension analysis showed that about half the transcripts were edited. Sequences of the P, C and V proteins encoded by the normal and edited transcripts were compared with those of other morbilliviruses and with those of the more distantly related paramyxoviruses.
我们克隆了几个源自牛瘟病毒P基因的cDNA。其中一个源自双顺反子N-P mRNA,已对其进行了全序列测定。对其他部分进行测序,并与基因组序列进行比较,结果表明,与其他麻疹病毒一样,P基因转录本是可变的;在一个类似于正常终止转录位点的位置可以添加非模板化的G。引物延伸分析表明,约一半的转录本被编辑。将正常转录本和编辑转录本编码的P、C和V蛋白的序列与其他麻疹病毒以及亲缘关系更远的副粘病毒的序列进行了比较。