Evidence map›Paper›PMID 23821034›Full record

ArticleDevelopment (Cambridge, England)2013

The miR-310/13 cluster antagonizes β-catenin function in the regulation of germ and somatic cell differentiation in the Drosophila testis.

Raluca Pancratov, Felix Peng, Peter Smibert, Shiuan Yang, Emily Ruth Olson, Ciaran Guha-Gilford, Amol J Kapoor, Feng-Xia Liang, Eric C Lai, Maria Sol Flaherty and 1 more

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.3field-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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  11. The role of integrins inDevelopment (Cambridge, England) · 2019
    Article
  12. Review
  13. Review
  14. Article
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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

11 authors at 2 institutions in 1 country.

Raluca PancratovDepartment of Pharmacology and the NYU Cancer Institute, New York University Langone Medical Center, 522 First Avenue, SRB #1211, New York, NY 10016, USA.
Felix Peng
Peter Smibert
Shiuan Yang
Emily Ruth Olson
Ciaran Guha-Gilford
Amol J Kapoor
Feng-Xia Liang
Eric C Lai
Maria Sol Flaherty
Ramanuj DasgGupta
NYU Langone Health · USKettering University · US

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
Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Targeted Screen for Novel Chemical Modulators of Wnt/Beta-Cat Signaling Pathway.R01CA155125 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DASGUPTA, RAMANUJ, DYNLACHT, BRIAN D · 2012 to 2015
$1.5M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA155125NIGMS NIH HHS R01 GM083300NIGMS NIH HHS R01-GM083300NIGMS NIH HHS R01 GM084947NIGMS NIH HHS R01-GM084947
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are regulators of global gene expression and function in a broad range of biological processes. Recent studies have suggested that miRNAs can function as tumor suppressors or oncogenes by modulating the activities of evolutionarily conserved signaling pathways that are commonly dysregulated in cancer. We report the identification of the miR-310 to miR-313 (miR-310/13) cluster as a novel antagonist of Wingless (Drosophila Wnt) pathway activity in a functional screen for Drosophila miRNAs. We demonstrate that miR-310/13 can modulate Armadillo (Arm; Drosophila β-catenin) expression and activity by directly targeting the 3'-UTRs of arm and pangolin (Drosophila TCF) in vivo. Notably, the miR-310/13-deficient flies exhibit abnormal germ and somatic cell differentiation in the male gonad, which can be rescued by reducing Arm protein levels or activity. Our results implicate a previously unrecognized function for miR-310/13 in dampening the activity of Arm in early somatic and germline progenitor cells, whereby inappropriate/sustained activation of Arm-mediated signaling or cell adhesion may impact normal differentiation in the Drosophila male gonad.

Indexed as

Cell Differentiation3' Untranslated RegionsAnimalsArmadillo Domain ProteinsDrosophilaDrosophila ProteinsGerm CellsMaleMicroRNAsRepressor ProteinsSignal TransductionTestisTranscription Factors3' Untranslated RegionsArmadillo Domain ProteinsARM protein, DrosophilaDrosophila ProteinsMicroRNAsMIRN310 microRNA, Drosophilapan protein, DrosophilaRepressor ProteinsTranscription FactorsArmadilloBeta-cateninMicroRNAStem cellsWingless

Identifiers

PMID23821034
PMCPMC3699279
OpenAlexW2140962206

What OpenQuestion holds

Textmetadata
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.