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Recurrent emergence of structural variants of LTR retrotransposon CsRn1 evolving novel expression strategy and their selective expansion in a carcinogenic liver fluke, Clonorchis sinensis

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dc.contributor.authorKim, Seon-Hee-
dc.contributor.authorKong, Yoon-
dc.contributor.authorBae, Young-An-
dc.date.available2020-02-27T18:43:00Z-
dc.date.created2020-02-06-
dc.date.issued2017-06-
dc.identifier.issn0166-6851-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/6095-
dc.description.abstractAutonomous retrotransposons, in which replication and transcription are coupled, encode the essential gag and pol genes as a fusion or separate overlapping form(s) that are expressed in single transcripts regulated by a common upstream promoter. The element-specific expression strategies have driven development of relevant translational recoding mechanisms including ribosomal frameshifting to satisfy the protein stoichiometry critical for the assembly of infectious virus-like particles. Retrotransposons with different recoding strategies exhibit a mosaic distribution pattern across the diverse families of reverse transcribing elements, even though their respective distributions are substantially skewed towards certain family groups. However, only a few investigations to date have focused on the emergence of retrotransposons evolving novel expression strategy and causal genetic drivers of the structural variants. In this study, the bulk of genomic and transcribed sequences of a Ty3/gypsy-like CsRn1 retrotransposon in Clonorchis sinensis were analyzed for the comprehensive examination of its expression strategy. Our results demonstrated that structural variants with single open reading frame (ORF) have recurrently emerged from precedential CsRn1 copies encoding overlapping gag-pol ORFs by a single nucleotide insertion in an upstream region of gag stop codon. In the parasite genome, some of the newly evolved variants appeared to undergo proliferative burst as active master lineages together with their ancestral copies. The genetic event was similarly observed in Opisthorchis viverrini, the closest neighbor of C. sinensis, whereas the resulting structural variants might have failed to overcome purifying selection and comprised minor remnant copies in the Opisthorchis genome. (C) 2017 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.relation.isPartOfMOLECULAR AND BIOCHEMICAL PARASITOLOGY-
dc.subjectVIRUS-LIKE PARTICLES-
dc.subjectDROSOPHILA 1731 RETROTRANSPOSON-
dc.subjectLONG TERMINAL REPEAT-
dc.subjectTRANSCRIPTIONAL SLIPPAGE-
dc.subjectINFECTIOUS RETROVIRUS-
dc.subjectTRANSPOSABLE ELEMENTS-
dc.subjectPHYLOGENETIC ANALYSIS-
dc.subjectESCHERICHIA-COLI-
dc.subjectMELANOGASTER-
dc.subjectPROTEIN-
dc.titleRecurrent emergence of structural variants of LTR retrotransposon CsRn1 evolving novel expression strategy and their selective expansion in a carcinogenic liver fluke, Clonorchis sinensis-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000404795200003-
dc.identifier.doi10.1016/j.molbiopara.2017.03.004-
dc.identifier.bibliographicCitationMOLECULAR AND BIOCHEMICAL PARASITOLOGY, v.214, pp.14 - 26-
dc.identifier.scopusid2-s2.0-85015980932-
dc.citation.endPage26-
dc.citation.startPage14-
dc.citation.titleMOLECULAR AND BIOCHEMICAL PARASITOLOGY-
dc.citation.volume214-
dc.contributor.affiliatedAuthorKim, Seon-Hee-
dc.contributor.affiliatedAuthorBae, Young-An-
dc.type.docTypeArticle-
dc.subject.keywordAuthorLTR retrotransposon-
dc.subject.keywordAuthorClonorchis sinensis-
dc.subject.keywordAuthorCsRn1-
dc.subject.keywordAuthorExpression strategy-
dc.subject.keywordAuthorORF fusion-
dc.subject.keywordAuthorFrameshifting-
dc.subject.keywordPlusVIRUS-LIKE PARTICLES-
dc.subject.keywordPlusDROSOPHILA 1731 RETROTRANSPOSON-
dc.subject.keywordPlusLONG TERMINAL REPEAT-
dc.subject.keywordPlusTRANSCRIPTIONAL SLIPPAGE-
dc.subject.keywordPlusINFECTIOUS RETROVIRUS-
dc.subject.keywordPlusTRANSPOSABLE ELEMENTS-
dc.subject.keywordPlusPHYLOGENETIC ANALYSIS-
dc.subject.keywordPlusESCHERICHIA-COLI-
dc.subject.keywordPlusMELANOGASTER-
dc.subject.keywordPlusPROTEIN-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaParasitology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryParasitology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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