Single polysome analysis of mRNP

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dc.contributor.authorKim Byungjuko
dc.contributor.authorPark Yeonkyoungko
dc.contributor.authorHwang Hyun Jungko
dc.contributor.authorChang Jeeyoonko
dc.contributor.authorKim Yoon Kiko
dc.contributor.authorLee Jong-Bongko
dc.date.accessioned2022-08-10T01:00:09Z-
dc.date.available2022-08-10T01:00:09Z-
dc.date.created2022-08-09-
dc.date.created2022-08-09-
dc.date.created2022-08-09-
dc.date.created2022-08-09-
dc.date.created2022-08-09-
dc.date.created2022-08-09-
dc.date.issued2022-08-
dc.identifier.citationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.618, pp.73 - 78-
dc.identifier.issn0006-291X-
dc.identifier.urihttp://hdl.handle.net/10203/297908-
dc.description.abstractEukaryotic translation is a complex process that involves the interplay of various translation factors to convert genetic information into a specific amino acid chain. According to an elegant model of eukaryotic translation initiation, the 3' poly(A) tail of an mRNA, which is occupied by poly(A)-binding proteins (PABPs), communicates with the 5'-cap bound by eIF4E to enhance translation. Although the circulari-zation of mRNA resulting from the communication is widely understood, it has yet to be directly observed. To explore mRNA circularization in translation, we analyzed the level of colocalization of eIF4E, eIF4G, and PABP on individual mRNAs in polysomal and subpolysomal fractions using single polysome analysis. Our results show that the three tested proteins barely coexist in mRNA in either polysomal or subpolysomal fractions, implying that the closed-loop structure generated by the communication be-tween eIF4E, eIF4G, and PAPB may be transient during translation. (C) 2022 The Authors. Published by Elsevier Inc.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleSingle polysome analysis of mRNP-
dc.typeArticle-
dc.identifier.wosid000827684400011-
dc.identifier.scopusid2-s2.0-85132360662-
dc.type.rimsART-
dc.citation.volume618-
dc.citation.beginningpage73-
dc.citation.endingpage78-
dc.citation.publicationnameBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.identifier.doi10.1016/j.bbrc.2022.06.017-
dc.contributor.localauthorKim Yoon Ki-
dc.contributor.nonIdAuthorKim Byungju-
dc.contributor.nonIdAuthorPark Yeonkyoung-
dc.contributor.nonIdAuthorHwang Hyun Jung-
dc.contributor.nonIdAuthorChang Jeeyoon-
dc.contributor.nonIdAuthorLee Jong-Bong-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorPoly(A) tail-
dc.subject.keywordAuthormRNA-
dc.subject.keywordAuthorTranslation-
dc.subject.keywordAuthorClosed-loop model-
dc.subject.keywordAuthorPolysome-
dc.subject.keywordAuthorPABP(PABPC1)-
dc.subject.keywordPlusEUKARYOTIC TRANSLATION INITIATION-
dc.subject.keywordPlusPOLY(A) TAIL LENGTH-
dc.subject.keywordPlusCLOSED-LOOP MODEL-
dc.subject.keywordPlusPOLY(A)-BINDING PROTEIN-
dc.subject.keywordPlusRNA MOLECULES-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusREVEALS-
dc.subject.keywordPlusPABP-
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