pubmed-article:9041391 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9041391 | lifeskim:mentions | umls-concept:C0949920 | lld:lifeskim |
pubmed-article:9041391 | lifeskim:mentions | umls-concept:C1527239 | lld:lifeskim |
pubmed-article:9041391 | lifeskim:mentions | umls-concept:C0025663 | lld:lifeskim |
pubmed-article:9041391 | lifeskim:mentions | umls-concept:C0205147 | lld:lifeskim |
pubmed-article:9041391 | lifeskim:mentions | umls-concept:C0035681 | lld:lifeskim |
pubmed-article:9041391 | lifeskim:mentions | umls-concept:C1335440 | lld:lifeskim |
pubmed-article:9041391 | lifeskim:mentions | umls-concept:C1555029 | lld:lifeskim |
pubmed-article:9041391 | lifeskim:mentions | umls-concept:C0242494 | lld:lifeskim |
pubmed-article:9041391 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:9041391 | pubmed:dateCreated | 1997-6-2 | lld:pubmed |
pubmed-article:9041391 | pubmed:abstractText | Amplification of a 3-kb genome region from the RNA polymerase gene to the 3' poly(A) tail of small round-structured virus (SRSV) by reverse transcription-PCR (RT-PCR) has been difficult to achieve because of a stable secondary structure in a region between the RNA polymerase gene and the 5' end of the second open reading frame. We have developed a one-tube RT-PCR method to efficiently amplify this region. The method comprises three procedures: purification of poly(A)+ RNA from a starting RNA solution by oligo(dT)30 covalently linked to latex particles, buffer exchange, and continuous RT and PCR in a single tube containing all reaction components. The key elements of this method are (i) first-strand cDNA synthesis with the Superscript II version of RNase H- Moloney murine leukemia virus reverse transcriptase at 50 degrees C for 10 min by using the RNA-oligo(dT)30 hybrid on the latex particles as the template and primer, and (ii) PCR by Taq and Pwo DNA polymerases mixed together with a mixture of 12 phased oligo(dT)25 antisense primers. The detection threshold of the one-tube RT-PCR method was as little as 0.2 ng of the crude RNA used as the source of the template. Using this method, we obtained 3-kb products from 24 SRSV strains previously characterized into four genetic groups. These included 5 P1-A, 4 P1-B, 5 P2-A, and 10 P2-B strains. Because SRSVs have not yet been cultivated in vitro, this novel method should facilitate molecular characterization of SRSVs to provide a firm scientific foundation for improvements and refinements of SRSV diagnostics. | lld:pubmed |
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pubmed-article:9041391 | pubmed:language | eng | lld:pubmed |
pubmed-article:9041391 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9041391 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:9041391 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:9041391 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9041391 | pubmed:month | Mar | lld:pubmed |
pubmed-article:9041391 | pubmed:issn | 0095-1137 | lld:pubmed |
pubmed-article:9041391 | pubmed:author | pubmed-author:AndoTT | lld:pubmed |
pubmed-article:9041391 | pubmed:author | pubmed-author:GlassR IRI | lld:pubmed |
pubmed-article:9041391 | pubmed:author | pubmed-author:NoelJ SJS | lld:pubmed |
pubmed-article:9041391 | pubmed:author | pubmed-author:MonroeS SSS | lld:pubmed |
pubmed-article:9041391 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9041391 | pubmed:volume | 35 | lld:pubmed |
pubmed-article:9041391 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9041391 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9041391 | pubmed:pagination | 570-7 | lld:pubmed |
pubmed-article:9041391 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:9041391 | pubmed:year | 1997 | lld:pubmed |
pubmed-article:9041391 | pubmed:articleTitle | A one-tube method of reverse transcription-PCR to efficiently amplify a 3-kilobase region from the RNA polymerase gene to the poly(A) tail of small round-structured viruses (Norwalk-like viruses). | lld:pubmed |
pubmed-article:9041391 | pubmed:affiliation | Viral Gastroenteritis Section, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA. txa5@CIDDVD1.em.cdc.gov | lld:pubmed |
pubmed-article:9041391 | pubmed:publicationType | Journal Article | lld:pubmed |
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