cDNA sequences for asialoglycoprotein receptor from human fetal liver

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dc.contributor.authorDong Gun Lee-
dc.contributor.authorSung Gu Lee-
dc.contributor.authorKil Lyong Kim-
dc.contributor.authorKyung Soo Hahm-
dc.date.accessioned2017-04-19T08:54:49Z-
dc.date.available2017-04-19T08:54:49Z-
dc.date.issued1997-
dc.identifier.issn1225-8687-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/4193-
dc.description.abstractThe asialoglycoprotein receptor (ASGPR) was the first described mammalian lectin that mediates the specific binding and internalization of galactose/N-acetylgalactosamine-terminating glycoproteins by hepatic parenchymal cells. H1 and H2 are known as essential subunits of the functional ASGPR. There were close similarities in ASGPR H2 subunits between cultured cell line HepG2 and normal human liver cells including identical sequences at both termini. It was therefore expected that there may be some similarities between the subunits from normal liver cells and fetal liver cells. The two subunits of human fetal liver ASGPR, designated FL-H1 and FL-H2, were cloned from cDNA library by PCR and the sequences were compared with the known H1 and H2 sequences of HepG2, and the H1 sequence of nomal human liver cells. The results showed that FL-H1 was identical to H1 of HepG2. Whereas FL-H2 contains a 15-bp miniexon, but missing 57-bp at the near upstream from the membrane-spanning domain compared to H2 of HepG2 and normal human liver cells indicating that FL-H2 resulted from a differential splicing compared to HepG2 and normal liver cells.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titlecDNA sequences for asialoglycoprotein receptor from human fetal liver-
dc.title.alternativecDNA sequences for asialoglycoprotein receptor from human fetal liver-
dc.typeArticle-
dc.citation.titleBMB Reports-
dc.citation.number4-
dc.citation.endPage301-
dc.citation.startPage299-
dc.citation.volume30-
dc.contributor.affiliatedAuthorDong Gun Lee-
dc.contributor.affiliatedAuthorSung Gu Lee-
dc.contributor.affiliatedAuthorKil Lyong Kim-
dc.contributor.affiliatedAuthorKyung Soo Hahm-
dc.contributor.alternativeName이동건-
dc.contributor.alternativeName이성구-
dc.contributor.alternativeName김길룡-
dc.contributor.alternativeName함경수-
dc.identifier.bibliographicCitationBMB Reports, vol. 30, no. 4, pp. 299-301-
dc.subject.keywordHepatitis B virus-
dc.subject.keywordHepG2-
dc.subject.keywordMiniexon-
dc.subject.keywordPolymerase chain reaction-
dc.subject.keywordpreS1-
dc.subject.localHepatitis B Virus-
dc.subject.localHepatitis B virus-
dc.subject.localHepatitis B virus (HBV)-
dc.subject.localhepatitis B Virus (HBV)-
dc.subject.localhepatitis B virus-
dc.subject.localhepatitis B virus (HBV)-
dc.subject.localHepG2-
dc.subject.localMiniexon-
dc.subject.localPolymerase Chain Reaction-
dc.subject.localPolymerase chain reaction-
dc.subject.localPolymerase chain reaction (PCR)-
dc.subject.localPCR-
dc.subject.localPCR, polymerase chain reaction-
dc.subject.localpolymerase chain reaction-
dc.subject.localPreS1-
dc.subject.localpreS1-
dc.description.journalClassY-
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