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Terminal Uridylyltransferases Execute Programmed Clearance of Maternal Transcriptome in Vertebrate Embryos

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dc.contributor.authorHyeshik Chang-
dc.contributor.authorJinah Yeo-
dc.contributor.authorJeong-gyun Kim-
dc.contributor.authorHyunjoon Kim-
dc.contributor.authorJaechul Lim-
dc.contributor.authorMihye Lee-
dc.contributor.authorHyun Ho Kim-
dc.contributor.authorJiyeon Ohk-
dc.contributor.authorHee-Yeon Jeon-
dc.contributor.authorHyunsook Lee-
dc.contributor.authorHosung Jung-
dc.contributor.authorKyu-Won Kim-
dc.contributor.authorV. Narry Kim-
dc.date.available2018-07-18T02:03:43Z-
dc.date.created2018-06-21-
dc.date.issued2018-04-
dc.identifier.issn1097-2765-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/4554-
dc.description.abstractDuring the maternal-to-zygotic transition (MZT),maternal RNAs are actively degraded and replaced by newly synthesized zygotic transcripts in a highly coordinated manner. However, it remains largely unknown how maternal mRNA decay is triggered in early vertebrate embryos. Here, through genomewide profiling of RNA abundance and 30 modification, we show that uridylation is induced at the onset of maternal mRNA clearance. The temporal control of uridylation is conserved in vertebrates. When the homologs of terminal uridylyltransferases TUT4 and TUT7 (TUT4/7) are depleted in zebrafish and Xenopus, maternal mRNA clearance is significantly delayed, leading to developmental defects during gastrulation. Short-tailed mRNAs are selectively uridylated by TUT4/7, with the highly uridylated transcripts degraded faster during the MZT than those with unmodified poly(A) tails. Our study demonstrates that uridylation plays a crucial role in timely mRNA degradation, thereby allowing the progression of early development. (c) 2018 Elsevier Inc.-
dc.description.uri1-
dc.language영어-
dc.publisherCELL PRESS-
dc.titleTerminal Uridylyltransferases Execute Programmed Clearance of Maternal Transcriptome in Vertebrate Embryos-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000429301100009-
dc.identifier.scopusid2-s2.0-85044567635-
dc.identifier.rimsid63953ko
dc.contributor.affiliatedAuthorHyeshik Chang-
dc.contributor.affiliatedAuthorJinah Yeo-
dc.contributor.affiliatedAuthorHyunjoon Kim-
dc.contributor.affiliatedAuthorJaechul Lim-
dc.contributor.affiliatedAuthorMihye Lee-
dc.contributor.affiliatedAuthorV. Narry Kim-
dc.identifier.doi10.1016/j.molcel.2018.03.004-
dc.identifier.bibliographicCitationMOLECULAR CELL, v.70, no.1, pp.72 - 82-
dc.citation.titleMOLECULAR CELL-
dc.citation.volume70-
dc.citation.number1-
dc.citation.startPage72-
dc.citation.endPage82-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
Center for RNA Research(RNA 연구단) > 1. Journal Papers (저널논문)
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