Protein-protein interaction among hnRNPs shuttling between nucleus and cytoplasm

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dc.contributor.authorKim, JHko
dc.contributor.authorHahm, Bko
dc.contributor.authorKim, Yoon Kiko
dc.contributor.authorChoi, MYko
dc.contributor.authorJang, SKko
dc.date.accessioned2022-08-04T06:02:30Z-
dc.date.available2022-08-04T06:02:30Z-
dc.date.created2022-08-04-
dc.date.created2022-08-04-
dc.date.issued2000-05-
dc.identifier.citationJOURNAL OF MOLECULAR BIOLOGY, v.298, no.3, pp.395 - 405-
dc.identifier.issn0022-2836-
dc.identifier.urihttp://hdl.handle.net/10203/297791-
dc.description.abstractHeterogeneous nuclear ribonucleoproteins (hnRNPs) are involved in several RNA-related biological processes such as transcription, pre-mRNA processing, mature mRNA transport to the cytoplasm, and translation. About 20 major hnRNPs from A1 to U are known. Among them, hnRNP A, D, E, I, and K are known to shuttle between the nucleus and the cytoplasm. hnRNP E2 has been seen to stabilize alpha-globin mRNA and to enhance polioviral mRNA translation. hnRNP K modulates transcription and translation of some mRNAs. hnRNP I and its homologue hnRNP L have been suggested to enhance translation of some IRES-dependent mRNAs. In order to better understand the molecular mechanisms of the biological functions of hnRNPs, we investigated protein-protein interactions of six hnRNPs (hnRNP Al, C1, E2, I, K, and L) using the yeast two-hybrid system and in vitro co-precipitation assays. All of the hnRNPs tested exerted homomeric interactions, and hnRNP E2, I, K, and L interacted with each other. In the case of hnRNP E2 and hnRNP K, the N-terminal half of the proteins containing two KH (K homologous) domains were required for protein-protein interaction, and the second quarter of hnRNP I and hnRNP L containing RRM2 (RNA recognition motif 2) was essential for protein-protein interaction. hnRNP A1 and C1 did not form complexes with other hnRNPs in our assay systems. This suggests that the hnRNPs could fall into two groups: one group, including hnRNP A1 and C1, involved in hnRNP core complex formation and another group, including hnRNP E2, I, K, and L, involved in a variety of RNA-related biological processes. Different combinations of the proteins of the second group may facilitate different biological processes in conjunction with other factors. (C) 2000 Academic Press.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD-
dc.titleProtein-protein interaction among hnRNPs shuttling between nucleus and cytoplasm-
dc.typeArticle-
dc.identifier.wosid000086985100005-
dc.identifier.scopusid2-s2.0-0034607554-
dc.type.rimsART-
dc.citation.volume298-
dc.citation.issue3-
dc.citation.beginningpage395-
dc.citation.endingpage405-
dc.citation.publicationnameJOURNAL OF MOLECULAR BIOLOGY-
dc.identifier.doi10.1006/jmbi.2000.3687-
dc.contributor.localauthorKim, Yoon Ki-
dc.contributor.nonIdAuthorKim, JH-
dc.contributor.nonIdAuthorHahm, B-
dc.contributor.nonIdAuthorChoi, MY-
dc.contributor.nonIdAuthorJang, SK-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorshuttling hnRNPs-
dc.subject.keywordAuthorprotein-protein interaction-
dc.subject.keywordAuthoryeast two-hybrid-
dc.subject.keywordAuthorin vitro co-precipitation-
dc.subject.keywordAuthorRNA-related processes-
dc.subject.keywordPlusTRACT-BINDING-PROTEIN-
dc.subject.keywordPlusMESSENGER-RNA STABILITY-
dc.subject.keywordPlusINTERNAL RIBOSOMAL ENTRY-
dc.subject.keywordPlusRIBONUCLEOPROTEIN-K-
dc.subject.keywordPlusTRANSCRIPTION FACTOR-
dc.subject.keywordPlus5&apos-
dc.subject.keywordPlus-NONCODING REGION-
dc.subject.keywordPlusPOLIOVIRUS RNA-
dc.subject.keywordPlusC-PROTEINS-
dc.subject.keywordPlusVIRUS-RNA-
dc.subject.keywordPlusDOMAIN-
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