Methods for cDNA cloning and sequencing tobacco mosaic virus RNA
Identifieur interne : 004E39 ( Main/Exploration ); précédent : 004E38; suivant : 004E40Methods for cDNA cloning and sequencing tobacco mosaic virus RNA
Auteurs : Philip Goelet ; Jonathan KarnSource :
- Gene [ 0378-1119 ] ; 1984.
English descriptors
- Teeft :
- Alkaline hydrolysis, Bumhi, Bumhi linkers, Cdna, Cdna clones, Cdna fragments, Cdna products, Cdna recombinants, Cdna sequences, Cdna synthesis, Clone, Computer methods, Digestion, Dsdna, Dsdna synthesis, Genome, Klenow, Ligation, Linkers, Mike gait, Nuclease, Nucleotide, Oligonucleotide, Oligonucleotides, Phenol, Phenol extraction, Polymerase, Primer, Rapid cooling, Recombinant, Restriction endonucleases, Restriction fragments, Sau3a, Second strand, Sequence analysis, Sequencing, Short oligonucleotides, Specific cdna, Synthesis reaction, Synthetic oligonucleotides, Terminal transferase, Tobacco mosaic virus, Transcription, Transcription reaction, Transferase.
Abstract
Abstract: DNA complementary to tobacco mosaic virus (TMV) RNA (cDNA) was prepared by priming reverse transcription with synthetic oligonucleotides. The cDNAs terminated prematurely at many specific sites and no transcripts longer than about 2000 nucleotides were obtained. However, the entire 6395 nucleotide long TMV RNA could be copied into cDNA by specific priming with a series of 13 to 17 residue long oligonucleotides or by non-specific priming with short, 4 to 7 residue, oligonucleotides. A number of different priming methods were used to convert the cDNA into double-stranded DNA (dsDNA). The double-stranded cDNA was recovered by shotgun cloning into M13 and analysed by sequencing. The frequency at which cDNA clones were recovered has been used to compare various cDNA cloning strategies.
Url:
DOI: 10.1016/0378-1119(84)90062-3
Affiliations:
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Le document en format XML
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The cDNAs terminated prematurely at many specific sites and no transcripts longer than about 2000 nucleotides were obtained. However, the entire 6395 nucleotide long TMV RNA could be copied into cDNA by specific priming with a series of 13 to 17 residue long oligonucleotides or by non-specific priming with short, 4 to 7 residue, oligonucleotides. A number of different priming methods were used to convert the cDNA into double-stranded DNA (dsDNA). The double-stranded cDNA was recovered by shotgun cloning into M13 and analysed by sequencing. The frequency at which cDNA clones were recovered has been used to compare various cDNA cloning strategies.</div></front></TEI><affiliations><list></list><tree><noCountry><name sortKey="Goelet, Philip" sort="Goelet, Philip" uniqKey="Goelet P" first="Philip" last="Goelet">Philip Goelet</name><name sortKey="Karn, Jonathan" sort="Karn, Jonathan" uniqKey="Karn J" first="Jonathan" last="Karn">Jonathan Karn</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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