Abstract
The position of an alternative polyadenylation [poly(A)] site at the 3' end of the polyomavirus middle T antigen (T-Ag) coding sequences suggests the possibility of a functional role for this site in early gene regulation. The fine structure of this alternative poly(A) site was determined by cDNA sequence and 3' S1 analyses. Cleavage-poly(A) was found to be heterogeneous, occurring at multiple CA dinucleotides downstream from the AATAAA signal sequence. About 50% of the alternative poly(A) takes place upstream from the middle T-Ag stop codon. In addition, the pattern of splicing of transcripts with the alternative poly(A) site differed from that with the major poly(A) site at the end of the early region. The ratio of the small and middle T-Ag splices to the large T-Ag splice for the alternative poly(A)+ mRNAs is about 2.5 times that found for mRNAs with the major poly(A) site. The altered splicing pattern and 3'-end heterogeneity of the alternative poly(A)+ mRNAs would result in preferential translation of small T-Ag (to a greater degree) and middle T-Ag over large T-Ag at later times in the polyomavirus lytic cycle.
MeSH Terms
Animals
Antigens, Polyomavirus Transforming/genetics
Base Sequence
Cell Line
Cell Line, Transformed
Fibroblasts
Gene Expression Regulation
Genes, Viral
Nucleic Acid Hybridization
Poly A/genetics
Polyomavirus/genetics,immunology
Protein Biosynthesis
RNA Splicing
RNA, Messenger/genetics
RNA, Viral/genetics
Transcription, Genetic
Chemicals
Antigens, Polyomavirus Transforming
RNA, Messenger
RNA, Viral
Poly A
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Norbury C J
Tumour Virus Genetics Laboratory, Imperial Cancer Research Fund, London, England.
Fried M
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