Molecular cloning, characterization and expression analysis of lipopolysaccharide-induced TNF-a factor (LITAF) gene from rock bream

DC Field Value Language
dc.contributor.author 채영선 -
dc.contributor.author 김하나 -
dc.contributor.author 김주원 -
dc.contributor.author 황성돈 -
dc.contributor.author 정지현 -
dc.contributor.author 심원준 -
dc.contributor.author 박찬일 -
dc.date.accessioned 2020-07-16T09:31:48Z -
dc.date.available 2020-07-16T09:31:48Z -
dc.date.created 2020-02-11 -
dc.date.issued 2013-05-08 -
dc.identifier.uri https://sciwatch.kiost.ac.kr/handle/2020.kiost/27085 -
dc.description.abstract The lipopolysaccharide-induced TNF-a factor (LITAF) is an important cytokine toregulate the innate immunity which plays major roles in regulating inflammatory, apoptosisand immune related genes. In this study, we identified and characterized rock bream(Oplegnathusfasciatus) LITAF gene. The full-length cDNA of LITAF1 and LITAF2 consistof 163 and 138 amino acids with a conserved LITAF domain that contain Zinc (Zn2+)binding structure and two of CXXC motif by multiple alignment. The expression analysisof LITAF1 mRNA in various tissue were performed using Quantitative real-time PCR. Thehighest mRNA expression level was detected in intestine. On the other hand, mRNAexpression of LITAF2 was detected in gill. In the expression analysis, mRNA expressionlevel of LITAF1 was significantly induced when infected with E. tarda, whereas, theexpression level of LITAF2 was induced by infection of S. iniae. LITAFs could beinduced by LPS (lipopolysaccharide), Gram-negative bacterial outer membrane. LITAF2was induced by Gram-positive bacterial, S. iniae. LITAF1 and 2 of rock bream hasimportant roles in infection such as activation of TNFSF (tumor necrosis factorsuperfamily) promoter.rized rock bream(Oplegnathusfasciatus) LITAF gene. The full-length cDNA of LITAF1 and LITAF2 consistof 163 and 138 amino acids with a conserved LITAF domain that contain Zinc (Zn2+)binding structure and two of CXXC motif by multiple alignment. The expression analysisof LITAF1 mRNA in various tissue were performed using Quantitative real-time PCR. Thehighest mRNA expression level was detected in intestine. On the other hand, mRNAexpression of LITAF2 was detected in gill. In the expression analysis, mRNA expressionlevel of LITAF1 was significantly induced when infected with E. tarda, whereas, theexpression level of LITAF2 was induced by infection of S. iniae. LITAFs could beinduced by LPS (lipopolysaccharide), Gram-negative bacterial outer membrane. LITAF2was induced by Gram-positive bacterial, S. iniae. LITAF1 and 2 of rock bream hasimportant roles in infection such as activation of TNFSF (tumor necrosis factorsuperfamily) promoter. -
dc.description.uri 2 -
dc.language English -
dc.publisher 한국해양학회 -
dc.relation.isPartOf 한국해양학회 -
dc.title Molecular cloning, characterization and expression analysis of lipopolysaccharide-induced TNF-a factor (LITAF) gene from rock bream -
dc.type Conference -
dc.citation.conferencePlace KO -
dc.citation.endPage 2494 -
dc.citation.startPage 2494 -
dc.citation.title 한국해양학회 -
dc.contributor.alternativeName 채영선 -
dc.contributor.alternativeName 김하나 -
dc.contributor.alternativeName 정지현 -
dc.contributor.alternativeName 심원준 -
dc.identifier.bibliographicCitation 한국해양학회, pp.2494 -
dc.description.journalClass 2 -
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