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Terminal Uridylyltransferases Execute Programmed Clearance of Maternal Transcriptome in Vertebrate Embryos

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dc.contributor.author정호성-
dc.date.accessioned2018-08-28T17:13:09Z-
dc.date.available2018-08-28T17:13:09Z-
dc.date.issued2018-
dc.identifier.issn1097-2765-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/162378-
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 genome-wide profiling of RNA abundance and 3' 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.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherCell Press-
dc.relation.isPartOfMOLECULAR CELL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleTerminal Uridylyltransferases Execute Programmed Clearance of Maternal Transcriptome in Vertebrate Embryos-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Anatomy-
dc.contributor.googleauthorHyeshik Chang-
dc.contributor.googleauthorJinah Yeo-
dc.contributor.googleauthorJeong-Gyun Kim-
dc.contributor.googleauthorHyunjoon Kim-
dc.contributor.googleauthorJaechul Lim-
dc.contributor.googleauthorMihye Lee-
dc.contributor.googleauthorHyun Ho Kim-
dc.contributor.googleauthorJiyeon Ohk-
dc.contributor.googleauthorHee-Yeon Jeon-
dc.contributor.googleauthorHyunsook Lee-
dc.contributor.googleauthorHosung Jung-
dc.contributor.googleauthorKyu-Won Kim-
dc.contributor.googleauthorV Narry Kim-
dc.identifier.doi10.1016/j.molcel.2018.03.004-
dc.contributor.localIdA03786-
dc.relation.journalcodeJ02256-
dc.identifier.eissn1097-4164-
dc.identifier.pmid29625039-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1097276518301850-
dc.subject.keywordRNA decay-
dc.subject.keywordTAIL-seq-
dc.subject.keywordTUT4-
dc.subject.keywordTUT7-
dc.subject.keywordU tail-
dc.subject.keywordZcchc11-
dc.subject.keywordZcchc6-
dc.subject.keywordmaternal-to-zygotic transition-
dc.subject.keywordpoly(A) tail-
dc.subject.keyworduridylation-
dc.contributor.alternativeNameJung, Ho Sung-
dc.contributor.affiliatedAuthorJung, Ho Sung-
dc.citation.volume70-
dc.citation.number1-
dc.citation.startPage72-
dc.citation.endPage82.e7-
dc.identifier.bibliographicCitationMOLECULAR CELL, Vol.70(1) : 72-82.e7, 2018-
dc.identifier.rimsid59962-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Anatomy (해부학교실) > 1. Journal Papers

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