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Selenocysteine tRNA[Ser]Sec, the central component of selenoprotein biosynthesis: Isolation, identification, modification, and sequencing

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dc.contributor.authorCarlson, Bradley A.-
dc.contributor.authorLee, Byeong Jae-
dc.contributor.authorTsuji, Petra A.-
dc.contributor.authorCopeland, Paul R.-
dc.contributor.authorSchweizer, Ulrich-
dc.contributor.authorGladyshev, Vadim N.-
dc.contributor.authorHatfield, Dolph L.-
dc.date.accessioned2024-05-27T08:48:25Z-
dc.date.available2024-05-27T08:48:25Z-
dc.date.created2020-10-26-
dc.date.issued2018-01-
dc.identifier.citationMethods in molecular biology (Clifton, N.J.), Vol.1661, pp.43-60-
dc.identifier.issn1064-3745-
dc.identifier.urihttps://hdl.handle.net/10371/203819-
dc.description.abstract© 2018, Springer Science+Business Media LLC.The selenocysteine (Sec) tRNA[Ser]Sec population consists of two isoforms that differ from each other by a single 2′-O-methylribosyl moiety at position 34 (Um34). These two isoforms, which are encoded in a single gene, Trsp, and modified posttranscriptionally, are involved individually in the synthesis of two subclasses of selenoproteins, designated housekeeping and stress-related selenoproteins. Techniques used in obtaining these isoforms for their characterization include extraction of RNA from mammalian cells and tissues, purifying the tRNA[Ser]Sec population by one or more procedures, and finally resolving the two isoforms from each other. Since some of the older techniques for isolating tRNA[Ser]Sec and resolving the isoforms are used in only a few laboratories, these procedures will be discussed briefly and references provided for more detailed information, while the more recently developed procedures are discussed in detail. In addition, a novel technique that was developed in sequencing tRNA[Ser]Sec for identifying their occurrence in other organisms is also presented.-
dc.language영어-
dc.publisherHumana Press, Inc.-
dc.titleSelenocysteine tRNA[Ser]Sec, the central component of selenoprotein biosynthesis: Isolation, identification, modification, and sequencing-
dc.typeArticle-
dc.identifier.doi10.1007/978-1-4939-7258-6_4-
dc.citation.journaltitleMethods in molecular biology (Clifton, N.J.)-
dc.identifier.scopusid2-s2.0-85029600081-
dc.citation.endpage60-
dc.citation.startpage43-
dc.citation.volume1661-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorLee, Byeong Jae-
dc.type.docTypeChapter-
dc.description.journalClass1-
dc.subject.keywordAuthorChromatography-
dc.subject.keywordAuthorGel electrophoresis-
dc.subject.keywordAuthorSelenium-
dc.subject.keywordAuthorSelenocysteine tRNA-
dc.subject.keywordAuthorSelenocysteine tRNA detection-
dc.subject.keywordAuthorSelenocysteine tRNA gene modification-
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