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Cloning and sequence analysis of the phosphoprotein gene of rinderpest virus

M. S. Shaila

AFRC Institute for Animal Health, Pirbright Laboratory, Ash Road, Woking, Surrey GU24 0NF, U.K.

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.

Present address: Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 56001, India.

Received 7 July 1992; accepted 29 September 1992.

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