1982
DOI: 10.1073/pnas.79.24.7644
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Cloning the double-stranded RNA genes of reovirus: sequence of the cloned S2 gene.

Abstract: The genes of the Dearing strain of reovirus serotype. 3, which consist of double-stranded RNA, have been cloned into pBR322 by tailing both strands ofeach gene with poly(A), transcribing them with reverse transcriptase, self-hybridizing the cognate plus and minus cDNA strands, incubating them with Ekcherichia coli DNA polymerase I to ensure that they are complete, and cloning the double-stranded cDNA molecules by standard procedures. The sequence of the cloned S2 gene has been determined. The sequences at the … Show more

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Cited by 78 publications
(57 citation statements)
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“…The sequence of the $2 gene of reovirus (Cashdollar et al, 1982) confirms the corresponding part of these data. From measurements of sequenced dsDNA standards by electron microscopy (Priess et al, 1980) a number of 1.91 × 106 mol.…”
supporting
confidence: 71%
“…The sequence of the $2 gene of reovirus (Cashdollar et al, 1982) confirms the corresponding part of these data. From measurements of sequenced dsDNA standards by electron microscopy (Priess et al, 1980) a number of 1.91 × 106 mol.…”
supporting
confidence: 71%
“…A genomic cDNA library from porcine C60 rotavirus was constructed using pUC 13 as cloning vector. In brief, total viral genomic dsRNA was 3' polyadenylated with E. coli poly(A) polymerase (Both et al, 1982;Cashdollar et al, 1982) and reverse transcribed by priming with oligo(dT) (Maniatis et al, 1982). The second cDNA strand was synthesized according to the method of Gubler & Hoffman (1983) and the ds cDNAs were blunt-end ligated to SmaI-cleaved and dephosphorylated pUC13.…”
Section: Cells and Virusesmentioning
confidence: 99%
“…The cDNA library of RGDV genome segments was made by the method of Cashdollar et al (1982). All dsRNA of RGDV was incubated in 90~ DMSO at 50 °C for 45 min, and then polyadenylated using poly(A) polymerase (Bethesda Research Laboratories).…”
mentioning
confidence: 99%