Evidence map›Paper›PMID 25330008›Full record

ArticlePLoS genetics2014

An integrated cell purification and genomics strategy reveals multiple regulators of pancreas development.

Cecil M Benitez, Kun Qu, Takuya Sugiyama, Philip T Pauerstein, Yinghua Liu, Jennifer Tsai, Xueying Gu, Amar Ghodasara, H Efsun Arda, Jiajing Zhang and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. RUNX1T1 function in cell fate.Stem cell research & therapy · 2022
    Review
  7. Single-cell transcriptome and accessible chromatin dynamics during endocrine pancreas development.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Mitofusin2 PromotesStem cells international · 2022
    Article
  9. Review
  10. Review
  11. The evolving landscape of NMolecular therapy : the journal of the American Society of Gene Therapy · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. The role of mMolecular cancer · 2019
    Review
  20. Article
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

14 authors at 3 institutions in 1 country.

Cecil M BenitezDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Kun QuProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Takuya SugiyamaDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Philip T PauersteinDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Yinghua LiuDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Jennifer TsaiDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Xueying GuDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Amar GhodasaraDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
H Efsun ArdaDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Jiajing ZhangProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, California, United States of America.
Joseph D DekkerInstitute for Cellular and Molecular Biology and Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas, United States of America.
Haley O TuckerInstitute for Cellular and Molecular Biology and Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas, United States of America.
Howard Y ChangProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, California, United States of America; Department of Dermatology, Stanford University School of Medicine,, Stanford, California, United States of America; Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California, United States of America.
Seung K KimDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America; Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California, United States of America; Department of Medicine (Oncology Division), Stanford University School of Medicine, Stanford, California, United States of America.
Stanford University · USThe University of Texas at Austin · USHoward Hughes Medical Institute · US

Funding

GENETICS TRAINING PROGRAM FOR PHD CANDIDATEST32GM007790 · NIGMS · STANFORD UNIVERSITY · PI BRUNET, ANNE, KINGSLEY, DAVID M · 1985 to 2020
$12.8M
GenomeSpace: A community web environment for integrative genomic analysisP01HG005062 · NHGRI · BROAD INSTITUTE, INC. · PI MESIROV, JILL P. · 2009 to 2013
$9.1M
MAR MEDIATED GENETIC SWITCH FOR IGH ENHANCER CONTROLR01CA031534 · NCI · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI TUCKER, HALEY O · 1985 to 2012
$2.9M
Howard Hughes Medical InstituteNCI NIH HHS CA-31534NCI NIH HHS R01 CA031534NHGRI NIH HHS P01 HG005062NHGRI NIH HHS P01-HG005062NIGMS NIH HHS T32 GM007790
6 · The paper itself

Abstract

The regulatory logic underlying global transcriptional programs controlling development of visceral organs like the pancreas remains undiscovered. Here, we profiled gene expression in 12 purified populations of fetal and adult pancreatic epithelial cells representing crucial progenitor cell subsets, and their endocrine or exocrine progeny. Using probabilistic models to decode the general programs organizing gene expression, we identified co-expressed gene sets in cell subsets that revealed patterns and processes governing progenitor cell development, lineage specification, and endocrine cell maturation. Purification of Neurog3 mutant cells and module network analysis linked established regulators such as Neurog3 to unrecognized gene targets and roles in pancreas development. Iterative module network analysis nominated and prioritized transcriptional regulators, including diabetes risk genes. Functional validation of a subset of candidate regulators with corresponding mutant mice revealed that the transcription factors Etv1, Prdm16, Runx1t1 and Bcl11a are essential for pancreas development. Our integrated approach provides a unique framework for identifying regulatory genes and functional gene sets underlying pancreas development and associated diseases such as diabetes mellitus.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBasic Helix-Loop-Helix ProteinsCell SeparationGenomicsInsulin-Secreting CellsMice, Mutant StrainsMice, TransgenicModels, StatisticalNerve Tissue ProteinsPancreasReproducibility of ResultsSOX9 Transcription FactorStem CellsBasic Helix-Loop-Helix ProteinsNerve Tissue ProteinsNeurog3 protein, mouseSox9 protein, mouseSOX9 Transcription Factor

Identifiers

PMID25330008
PMCPMC4199491
OpenAlexW1989163969

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.