Evidence map›Paper›PMID 23594738›Full record

ArticleNature2013

A role for the Perlman syndrome exonuclease Dis3l2 in the Lin28-let-7 pathway.

Hao-Ming Chang, Robinson Triboulet, James E Thornton, Richard I Gregory

Open access · greenAbstract read
In one paragraph

Article in Nature, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 221 papers.

0numbers the graph read from it
0cells of the map it votes in
221citing papers in PubMed
16.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

221 citing papers in PubMed, 338 citations in OpenAlex.

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  12. The biogenesis and regulation of animal microRNAs.Nature reviews. Molecular cell biology · 2025
    Review
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161 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Hao-Ming ChangStem Cell Program, Boston Children's Hospital, Massachusetts 02115, USA.
Robinson Triboulet
James E Thornton
Richard I Gregory
Harvard Stem Cell Institute · USBoston Children's Hospital · USHarvard University · US

Funding

Regulation of microRNA Biogenesis in Stem CellsR01GM086386 · NIGMS · BOSTON CHILDREN'S HOSPITAL · PI GREGORY, RICHARD I. · 2009 to 2018
$3.1M
NIGMS NIH HHS R01 GM086386NIGMS NIH HHS R01GM086386
6 · The paper itself

Abstract

The pluripotency factor Lin28 blocks the expression of let-7 microRNAs in undifferentiated cells during development, and functions as an oncogene in a subset of cancers. Lin28 binds to let-7 precursor (pre-let-7) RNAs and recruits 3' terminal uridylyl transferases to selectively inhibit let-7 biogenesis. Uridylated pre-let-7 is refractory to processing by Dicer, and is rapidly degraded by an unknown RNase. Here we identify Dis3l2 as the 3'-5' exonuclease responsible for the decay of uridylated pre-let-7 in mouse embryonic stem cells. Biochemical reconstitution assays show that 3' oligouridylation stimulates Dis3l2 activity in vitro, and knockdown of Dis3l2 in mouse embryonic stem cells leads to the stabilization of pre-let-7. Our study establishes 3' oligouridylation as an RNA decay signal for Dis3l2, and identifies the first physiological RNA substrate of this new exonuclease, which is mutated in the Perlman syndrome of fetal overgrowth and causes a predisposition to Wilms' tumour development.

Indexed as

RNA StabilityAnimalsCells, CulturedEmbryonic Stem CellsExonucleasesExoribonucleasesFetal MacrosomiaHEK293 CellsHumansMiceMicroRNAsRibonucleasesRNA-Binding ProteinsRNA PrecursorsRNA Processing, Post-TranscriptionalSubstrate Specificity3'-uridylic acidDis3l2 protein, mouseExonucleasesExoribonucleasesLin-28 protein, mouseMicroRNAsmirnlet7 microRNA, mouseRibonucleasesRNA-Binding ProteinsRNA PrecursorsUridine Monophosphate

Identifiers

PMID23594738
PMCPMC3651781
OpenAlexW2163636666

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.