共 31 条
Lin28 recruits the TUTase Zcchc11 to inhibit let-7 maturation in mouse embryonic stem cells
被引:408
作者:

Hagan, John P.
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机构:
Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol,Stem Cell Program, Childrens Hosp Boston,Harvard Med Sch, Boston, MA 02115 USA
Ohio State Univ, Med Ctr, Coll Med, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol,Stem Cell Program, Childrens Hosp Boston,Harvard Med Sch, Boston, MA 02115 USA

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Gregory, Richard I.
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机构:
Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol,Stem Cell Program, Childrens Hosp Boston,Harvard Med Sch, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol,Stem Cell Program, Childrens Hosp Boston,Harvard Med Sch, Boston, MA 02115 USA
机构:
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol,Stem Cell Program, Childrens Hosp Boston,Harvard Med Sch, Boston, MA 02115 USA
[2] Ohio State Univ, Med Ctr, Coll Med, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
关键词:
GENOME-WIDE ASSOCIATION;
MESSENGER-RNA;
IDENTIFICATION;
LOCI;
AGE;
MICRORNAS;
LIN-28;
OLIGOURIDYLATION;
URIDYLATION;
PATHWAYS;
D O I:
10.1038/nsmb.1676
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Lin28 and Lin28B, two developmentally regulated RNA-binding proteins and likely proto-oncogenes, selectively inhibit the maturation of let-7 family microRNAs (miRNAs) in embryonic stem cells and certain cancer cell lines. Moreover, let-7 precursors (pre-let-7) were previously found to be terminally uridylated in a Lin28-dependent fashion. Here we identify Zcchc11 ( zinc finger, CCHC domain containing 11) as the 3' terminal uridylyl transferase (TUTase) responsible for Lin28-mediated pre-let-7 uridylation and subsequent blockade of let-7 processing in mouse embryonic stem cells. We demonstrate that Zcchc11 activity is UTP-dependent, selective for let-7 and recruited by Lin28. Furthermore, knockdown of either Zcchc11 or Lin28, or overexpression of a catalytically inactive TUTase, relieves the selective inhibition of let-7 processing and leads to the accumulation of mature let-7 miRNAs and repression of let-7 target reporter genes. Our results establish a role for Zcchc11-catalyzed pre-let-7 uridylation in the control of miRNA biogenesis.
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页码:1021 / U33
页数:6
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