| Literature DB >> 29625039 |
Hyeshik Chang1, Jinah Yeo1, Jeong-Gyun Kim2, Hyunjoon Kim1, Jaechul Lim3, Mihye Lee1, Hyun Ho Kim2, Jiyeon Ohk4, Hee-Yeon Jeon5, Hyunsook Lee5, Hosung Jung4, Kyu-Won Kim2, V Narry Kim6.
Abstract
During 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.Entities:
Keywords: RNA decay; TAIL-seq; TUT4; TUT7; U tail; Zcchc11; Zcchc6; maternal-to-zygotic transition; poly(A) tail; uridylation
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Year: 2018 PMID: 29625039 DOI: 10.1016/j.molcel.2018.03.004
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970