Unusual features in the nucleotide sequence of a cDNA clone derived from the common region of avian sarcoma virus messenger RNA.

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Abstract
A recombinant plasmid containing a 700-base pair (bp) c[complementary]DNA copy of the common region present at the 3'' end of Schmidt-Ruppin avian sarcoma virus (ASV) 21S mRNA was constructed. The cDNA was inserted into [Escherichia coli] plasmid pBR322 at the Pst I site by the G-C tailing method. A restriction map of the cloned insert from a recombinant plasmid pSR1 indicates that it corresponds to the 3'' end of the ASV genome. R-loop analysis with ASV genomic RNA indicates that the insert is colinear with the ASV genome over most of its length. The sequence of 331 bp at the 3'' end of the DNA insert was determined and shows that the insert contains extra sequences not found at the 3'' end of ASV genomic RNA. Following the terminally redundant sequence of 20 bp that was found at the extreme 3'' end of genomic RNA is a sequence of 79 bp that is almost identical to that located immediately next to the 20-bp repeat at the 5'' end of ASV genomic RNA. This is followed by 18 bp of unique sequence, possibly of host origin. The structure of the clone suggests that ASV mRNA may differ from genomic RNA at its 3'' end and that 21S mRNA is transcribed from integrated ASV DNA and contains at its 3'' end sequences derived both from the 5'' end of the ASV genome and from host DNA adjacent to the site of integration. The presence of termination codons in all 3 reading frames suggests that the common region probably does not contain coding sequences. The presence of sequences that resemble probable promoter sites supports the possibility that this region may be involved in the regulation of transcription.