Evidence map›Paper›PMID 25636411›Full record

ArticleJournal of the American Society of Nephrology : JASN2015

Genome-Wide Analysis of Wilms' Tumor 1-Controlled Gene Expression in Podocytes Reveals Key Regulatory Mechanisms.

Martin Kann, Sandrine Ettou, Youngsook L Jung, Maximilian O Lenz, Mary E Taglienti, Peter J Park, Bernhard Schermer, Thomas Benzing, Jordan A Kreidberg

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
6.3field-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

69 citing papers in PubMed, 117 citations in OpenAlex.

  1. Article
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  10. Gene regulatory networks in disease and ageing.Nature reviews. Nephrology · 2024
    Review
  11. Article
  12. Article
  13. EGF-Receptor-Dependent TLR7 Signaling in Macrophages Promotes Glomerular Injury in Crescentic Glomerulonephritis.Laboratory investigation; a journal of technical methods and pathology · 2023
    Article
  14. A single-cell multiomic analysis of kidney organoid differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. Principles of human and mouse nephron development.Nature reviews. Nephrology · 2022
    Review
  17. Article
  18. Antisense oligonucleotides ameliorate kidney dysfunction in podocyte-specific APOL1 risk variant mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

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

9 authors at 5 institutions in 2 countries.

Martin KannDivision of Nephrology, Department of Medicine and Department II of Internal Medicine and Center for Molecular Medicine Cologne and.
Sandrine EttouDivision of Nephrology, Department of Medicine and.
Youngsook L JungCenter for Biomedical Informatics, Harvard Medical School, Boston, Massachusetts; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts;
Maximilian O LenzDepartment II of Internal Medicine and Center for Molecular Medicine Cologne and.
Mary E TaglientiDivision of Nephrology, Department of Medicine and.
Peter J ParkCenter for Biomedical Informatics, Harvard Medical School, Boston, Massachusetts; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts; Informatics Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts;
Bernhard SchermerDepartment II of Internal Medicine and Center for Molecular Medicine Cologne and Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases, Cologne, Germany; and Systems Biology of Ageing Cologne, University of Cologne, Cologne, Germany;
Thomas BenzingDepartment II of Internal Medicine and Center for Molecular Medicine Cologne and Cluster of Excellence on Cellular Stress Responses in Ageing-Associated Diseases, Cologne, Germany; and Systems Biology of Ageing Cologne, University of Cologne, Cologne, Germany; jordan.kreidberg@childrens.harvard.edu thomas.benzing@uk-koeln.de.
Jordan A KreidbergDivision of Nephrology, Department of Medicine and Harvard Stem Cell Institute, Cambridge, Massachusetts jordan.kreidberg@childrens.harvard.edu thomas.benzing@uk-koeln.de.
Brigham and Women's Hospital · USCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEHarvard Stem Cell Institute · USHarvard University · USUniversity of Cologne · DE

Funding

WT-1 IN UROGENITAL DEVELOPMENT AND TUMORIGENESISR01DK050118 · NIDDK · CHILDREN'S HOSPITAL BOSTON · PI KREIDBERG, JORDAN A. · 1997 to 2007
$2.3M
BMP and FGF Signaling in kidney progenitor cellsR01DK087794 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI KREIDBERG, JORDAN A · 2010 to 2013
$1.5M
NIDDK NIH HHS R01 DK050118NIDDK NIH HHS R01 DK087794NIDDK NIH HHS R01-DK087794-A1
6 · The paper itself

Abstract

The transcription factor Wilms' tumor suppressor 1 (WT1) is key to podocyte development and viability; however, WT1 transcriptional networks in podocytes remain elusive. We provide a comprehensive analysis of the genome-wide WT1 transcriptional network in podocytes in vivo using chromatin immunoprecipitation followed by sequencing (ChIPseq) and RNA sequencing techniques. Our data show a specific role for WT1 in regulating the podocyte-specific transcriptome through binding to both promoters and enhancers of target genes. Furthermore, we inferred a podocyte transcription factor network consisting of WT1, LMX1B, TCF21, Fox-class and TEAD family transcription factors, and MAFB that uses tissue-specific enhancers to control podocyte gene expression. In addition to previously described WT1-dependent target genes, ChIPseq identified novel WT1-dependent signaling systems. These targets included components of the Hippo signaling system, underscoring the power of genome-wide transcriptional-network analyses. Together, our data elucidate a comprehensive gene regulatory network in podocytes suggesting that WT1 gene regulatory function and podocyte cell-type specification can best be understood in the context of transcription factor-regulatory element network interplay.

Indexed as

Gene Expression RegulationPodocytesTranscriptomeAnimalsBasic Helix-Loop-Helix ProteinsChromatin ImmunoprecipitationForkhead Transcription FactorsGenomicsHippo Signaling PathwayLIM-Homeodomain ProteinsMafB Transcription FactorMiceProtein Serine-Threonine KinasesRepressor ProteinsSequence Analysis, DNASequence Analysis, RNABasic Helix-Loop-Helix ProteinsForkhead Transcription FactorsLIM homeobox transcription factor 1 betaLIM-Homeodomain ProteinsMafb protein, mouseMafB Transcription FactorProtein Serine-Threonine KinasesRepressor ProteinsTcf21 protein, mouseTranscription FactorsWT1 protein, mouseWT1 Proteinsgene expressiongenetics and developmentgene transcriptionglomerular diseaseglomeruluspodocyte

Identifiers

PMID25636411
PMCPMC4552122
OpenAlexW2149336866

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.