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Cited 11 time in webofscience Cited 16 time in scopus
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dc.contributor.authorLiang, CY-
dc.contributor.authorRieder, E-
dc.contributor.authorHahm, B-
dc.contributor.authorJang, SK-
dc.contributor.authorPaul, A-
dc.contributor.authorWimmer, E-
dc.date.accessioned2016-04-01T02:15:32Z-
dc.date.available2016-04-01T02:15:32Z-
dc.date.created2009-08-19-
dc.date.issued2005-03-01-
dc.identifier.issn0042-6822-
dc.identifier.other2005-OAK-0000004883-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/24771-
dc.description.abstractGenotype I a is a most prevalent genotype of hepatitis C virus in North America yet HCV replication has been studied predominantly with genotype 1b subgenomic replicons under neomycin selection in Huh-7 cells. Development of la-related dicistronic replicons under neo selection proved difficult and required either "conditioned' Huh-7 cells and/or chimeric genomes harboring pre-engineered adaptive mutations. We report the construction of a novel dicistronic genotype la(H77C) replicon expressing the puromycin N-acetyltranferase (PAC) gene as a selectable marker that, without prior introduction of adaptive mutations, allows establishment of puromycin-resistant Huh-7 colonies after transfection of naive Huh-7 cells. The large majority of HCV1a/PAC replicons did not reveal any adaptive mutations on short-term passage of Huh-7 cells. Continued passage led to mutations in the non-structural genes although these mutations did not significantly enhance replication of the original replicon. Transfection with total cellular RNA isolated from HCV1a/PAC replicon-containing cells led to a significant increase in colony-forming ability. The data identify PAC as an efficient selectable marker for studies of HCV replication, which may be useful with different genotypes in different host cell systems. (C) 2005 Elsevier Inc. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.relation.isPartOfVIROLOGY-
dc.subjecthepatitis C virus-
dc.subjectRNA replication-
dc.subjectgenotype 1a replicon-
dc.subjectpuromycin resistance gene-
dc.subjectHEPATITIS-C VIRUS-
dc.subjectRIBOSOMAL ENTRY SITE-
dc.subjectVIRAL-RNA REPLICATION-
dc.subjectEFFICIENT REPLICATION-
dc.subjectNONTRANSLATED REGION-
dc.subjectADAPTIVE MUTATIONS-
dc.subjectCDNA-CLONE-
dc.subjectCULTURE-
dc.subjectELEMENTS-
dc.subjectGENOME-
dc.titleReplication of a novel subgenomic HCV genotype 1a replicon expressing a puromycin resistance gene in Huh-7 cells-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1016/j.virol.2004.12.031-
dc.author.googleLiang, CY-
dc.author.googleRieder, E-
dc.author.googleHahm, B-
dc.author.googleJang, SK-
dc.author.googlePaul, A-
dc.author.googleWimmer, E-
dc.relation.volume333-
dc.relation.issue1-
dc.relation.startpage41-
dc.relation.lastpage53-
dc.contributor.id10088382-
dc.relation.journalVIROLOGY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationVIROLOGY, v.333, no.1, pp.41 - 53-
dc.identifier.wosid000227119000005-
dc.date.tcdate2019-02-01-
dc.citation.endPage53-
dc.citation.number1-
dc.citation.startPage41-
dc.citation.titleVIROLOGY-
dc.citation.volume333-
dc.contributor.affiliatedAuthorJang, SK-
dc.identifier.scopusid2-s2.0-13544275714-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc10-
dc.type.docTypeArticle-
dc.subject.keywordPlusHEPATITIS-C VIRUS-
dc.subject.keywordPlusRIBOSOMAL ENTRY SITE-
dc.subject.keywordPlusRNA REPLICATION-
dc.subject.keywordPlusEFFICIENT REPLICATION-
dc.subject.keywordPlusNONTRANSLATED REGION-
dc.subject.keywordPlusCDNA-CLONE-
dc.subject.keywordPlusELEMENTS-
dc.subject.keywordPlusINTERFERON-ALPHA-2B-
dc.subject.keywordPlusEPIDEMIOLOGY-
dc.subject.keywordPlusINITIATION-
dc.subject.keywordAuthorhepatitis C virus-
dc.subject.keywordAuthorRNA replication-
dc.subject.keywordAuthorgenotype 1a replicon-
dc.subject.keywordAuthorpuromycin resistance gene-
dc.relation.journalWebOfScienceCategoryVirology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaVirology-

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