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PMID: 8091677 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Canine oral papillomavirus genomic sequence: a unique 1.5-kb intervening sequence between the E2 and L2 open reading frames.

Virology ·Vol. 204 ·No. 1 ·1994-10-00 ·Pages 447-52

Delius H, Van Ranst MA, Jenson AB, zur Hausen H, Sundberg JP

Abstract

The canine oral papillomavirus (COPV) is associated with oropharyngeal papillomatosis in dogs, coyotes, and wolves. We have determined the complete nucleotide sequence of COPV, the largest of all known PV genomes (8607 bp). The genomic architecture of the COPV genome is similar to that of other PVs except for a unique and large noncoding region of 1.5 kb between the end of the early region (E2) and the beginning of the late region (L2) and a small (345 bp) upstream regulatory region between the end of L1 and the beginning of E6. Although COPV displays a primarily mucosal tropism, the COPV nucleotide sequence showed the highest overall similarity to cutaneous papillomaviruses such as HPV-1, HPV-63, CRPV (cottontail rabbit PV), FdPV (Felis domesticus PV), and MnPV (Mastomys natalensis PV).

MeSH Terms
Amino Acid Sequence Animals Base Sequence Dogs Genome, Viral Introns/genetics Molecular Sequence Data Open Reading Frames/genetics Papillomaviridae/genetics Sequence Analysis, DNA Sequence Homology, Nucleic Acid
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Delius H
Forschungsschwerpunkt Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg, Germany.
Van Ranst M A
Jenson A B
zur Hausen H
Sundberg J P
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1994-10-00
Pages
447-52
Language
English
Region
United States
NLM ID
0110674
Subset
IM
Grants
NCI NIH HHS · CA50182 · United States
NCI NIH HHS · CA57934 · United States
Databases
GENBANK
L22695
Analysis Services
Analysis Services

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