Evidence map›Paper›PMID 26145174›Full record

ArticleMolecular cell2015

Selective Suppression of the Splicing-Mediated MicroRNA Pathway by the Terminal Uridyltransferase Tailor.

Diane Bortolamiol-Becet, Fuqu Hu, David Jee, Jiayu Wen, Katsutomo Okamura, Ching-Jung Lin, Stefan L Ameres, Eric C Lai

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 70 citations in OpenAlex.

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  7. The biogenesis and regulation of animal microRNAs.Nature reviews. Molecular cell biology · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

Diane Bortolamiol-BecetSloan-Kettering Institute, Department of Developmental Biology, 1275 York Avenue, Box 252, New York, NY 10065, USA.
Fuqu HuSloan-Kettering Institute, Department of Developmental Biology, 1275 York Avenue, Box 252, New York, NY 10065, USA.
David JeeSloan-Kettering Institute, Department of Developmental Biology, 1275 York Avenue, Box 252, New York, NY 10065, USA; Biochemistry Cell and Molecular Biology Program, Weill Graduate School of Medical Sciences, Cornell University, New York, NY 10065, USA.
Jiayu WenSloan-Kettering Institute, Department of Developmental Biology, 1275 York Avenue, Box 252, New York, NY 10065, USA.
Katsutomo OkamuraTemasek Life Sciences Laboratory, 1 Research Link, National University of Singapore, Singapore 117604, Singapore; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore 639798, Singapore.
Ching-Jung LinSloan-Kettering Institute, Department of Developmental Biology, 1275 York Avenue, Box 252, New York, NY 10065, USA; Biochemistry Cell and Molecular Biology Program, Weill Graduate School of Medical Sciences, Cornell University, New York, NY 10065, USA.
Stefan L AmeresInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Dr. Bohr-Gasse 3, 1030 Vienna, Austria.
Eric C LaiSloan-Kettering Institute, Department of Developmental Biology, 1275 York Avenue, Box 252, New York, NY 10065, USA. Electronic address: laie@mskcc.org.
Kettering University · USCornell University · USInstitute of Molecular Biotechnology · ATNational University of Singapore · SG

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Selective regulatory and biogenesis mechanisms for microRNAsR01GM083300 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI Eric C Lai · 2007 to 2026
$9.8M
Mechanism and regulation of Hu family RNA binding proteins during neural alternative polyadenylationR01NS083833 · NINDS · SLOAN-KETTERING INST CAN RESEARCH · PI LAI, ERIC C · 2014 to 2023
$5.4M
TRAINING PROGRAM IN MOLECULAR AND CELLULAR BIOLOGYT32GM008539 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BROWN, ANTHONY M.C. · 1995 to 2020
$5.0M
NCI NIH HHS P30 CA008748NIGMS NIH HHS R01 GM083300NIGMS NIH HHS R01-GM083300NIGMS NIH HHS T32 GM008539NINDS NIH HHS R01 NS083833NINDS NIH HHS R01-NS083833
6 · The paper itself

Abstract

Several terminal uridyltransferases (TUTases) are known to modulate small RNA biogenesis and/or function via diverse mechanisms. Here, we demonstrate that Drosophila splicing-derived pre-miRNAs (mirtrons) are efficiently modified by the previously uncharacterized TUTase, Tailor. Tailor is necessary and sufficient for mirtron hairpin uridylation, and this modification inhibits mirtron biogenesis. Genome-wide analyses demonstrate that mirtrons are dominant Tailor substrates, and three features contribute to substrate specificity. First, reprogramming experiments show Tailor preferentially identifies splicing-derived miRNAs. Second, in vitro tests indicate Tailor prefers substrate hairpins over mature miRNAs. Third, Tailor exhibits sequence preference for 3'-terminal AG, a defining mirtron characteristic. Our work supports the notion that Tailor preferentially suppresses biogenesis of mirtrons, an evolutionarily adventitious pre-miRNA substrate class. Moreover, we detect preferential activity of Tailor on 3'-G canonical pre-miRNAs, and specific depletion of such loci from the pool of conserved miRNAs. Thus, Tailor activity may have had collateral impact on shaping populations of canonical miRNAs.

Indexed as

RNA SplicingAnimalsBase SequenceDrosophila melanogasterDrosophila ProteinsEvolution, MolecularFemaleGene Knockdown TechniquesGenes, InsectMicroRNAsNucleic Acid ConformationOvaryRNA NucleotidyltransferasesRNA Processing, Post-TranscriptionalSubstrate SpecificityDrosophila ProteinsMicroRNAsRNA NucleotidyltransferasesUTP-RNA uridylyltransferase

Identifiers

PMID26145174
PMCPMC4517475
OpenAlexW1556835664

What OpenQuestion holds

Textmetadata
LicenceTDM
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.