Evidence map›Paper›PMID 26932670›Full record

ArticleDevelopment (Cambridge, England)2016

GATA4 and GATA6 regulate pancreatic endoderm identity through inhibition of hedgehog signaling.

Shouhong Xuan, Lori Sussel

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
9.4field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Predictive control of human pancreatic cell fate using a digital model ofbioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Development of the Pancreatic Ducts and Their Contribution to Organogenesis.Advances in anatomy, embryology, and cell biology · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

2 authors at 1 institution in 1 country.

Shouhong XuanDepartment of Genetics and Development, Columbia University, New York, NY 10032, USA.
Lori SusselDepartment of Genetics and Development, Columbia University, New York, NY 10032, USA lgs2@cumc.columbia.edu.
Columbia University · US

Funding

Translational Biomarker Analytical Core (TBAC)P30DK063608 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI DOMENICO ACCILI · 2003 to 2026
$36.7M
Regulation of exocrine pancreas formationR01DK087711 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SUSSEL, LORI · 2010 to 2014
$1.7M
The role of Gata 4 in exocrine pancreas developmentR01DK064146 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI SUSSEL, LORI · 2003 to 2007
$1.3M
NIDDK NIH HHS P30 DK063608NIDDK NIH HHS R01 DK064146NIDDK NIH HHS R01 DK087711
6 · The paper itself

Abstract

GATA4 and GATA6 are zinc finger transcription factors that have important functions in several mesodermal and endodermal organs, including heart, liver and pancreas. In humans, heterozygous mutations of either factor are associated with pancreatic agenesis; however, homozygous deletion of both Gata4 and Gata6 is necessary to disrupt pancreas development in mice. In this study, we demonstrate that arrested pancreatic development in Gata4(fl/fl); Gata6(fl/fl); Pdx1:Cre (pDKO) embryos is accompanied by the transition of ventral and dorsal pancreatic fates into intestinal or stomach lineages, respectively. These results indicate that GATA4 and GATA6 play essential roles in maintaining pancreas identity by regulating foregut endodermal fates. Remarkably, pancreatic anlagen derived from pDKO embryos also display a dramatic upregulation of hedgehog pathway components, which are normally absent from the presumptive pancreatic endoderm. Consistent with the erroneous activation of hedgehog signaling, we demonstrate that GATA4 and GATA6 are able to repress transcription through the sonic hedgehog (Shh) endoderm-specific enhancer MACS1 and that GATA-binding sites within this enhancer are necessary for this repressive activity. These studies establish the importance of GATA4/6-mediated inhibition of hedgehog signaling as a major mechanism regulating pancreatic endoderm specification during patterning of the gut tube.

Indexed as

AnimalsBase SequenceBody PatterningCell LineageChromatin ImmunoprecipitationCoenzyme A LigasesEndodermGATA4 Transcription FactorGATA6 Transcription FactorGene Expression Regulation, DevelopmentalHedgehog ProteinsHeterozygoteMiceMice, KnockoutMitochondrial ProteinsMutationAcsm1 protein, mouseCoenzyme A LigasesGata4 protein, mouseGATA4 Transcription FactorGata6 protein, mouseGATA6 Transcription FactorHedgehog ProteinsMitochondrial ProteinsForegut endodermGATA4GATA6HedgehogMousePancreas

Identifiers

PMID26932670
PMCPMC4813334
OpenAlexW2313294278

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.