Evidence map›Paper›PMID 22820919›Full record

ArticleMolecules and cells2012

Glis3 regulates neurogenin 3 expression in pancreatic β-cells and interacts with its activator, Hnf6.

Yong-Sik Kim, Hong Soon Kang, Yukimasa Takeda, Lisa Hom, Ho-Yeon Song, Jan Jensen, Anton M Jetten

Abstract read
In one paragraph

Article in Molecules and cells, 2012. 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
2.9field-weighted citation impact, top 9% 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, 36 citations in OpenAlex.

  1. Predictive control of human pancreatic cell fate using a digital model ofbioRxiv : the preprint server for biology · 2026
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  20. Expanding the Clinical Spectrum Associated With GLIS3 Mutations.The Journal of clinical endocrinology and metabolism · 2015
    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

7 authors at 3 institutions in 2 countries.

Yong-Sik KimDepartment of Microbiology, College of Medicine, Soonchunhyang University, Cheonan 314-864, Korea. yongsikkim@sch.ac.kr
Hong Soon Kang
Yukimasa Takeda
Lisa Hom
Ho-Yeon Song
Jan Jensen
Anton M Jetten
National Institute of Environmental Health Sciences · USCleveland Clinic Lerner College of Medicine · USSoonchunhyang University · KR

Funding

Mechanism Of Action And Functions Of The Gli-related Proteins Glis 1-3ZIAES100485 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI JETTEN, ANTON M · 2009 to 2025
$35.9M
Epigenomics and DNA SequencingZICES102545 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI WADE, PAUL A · 2012 to 2025
$27.4M
Mechanism Of Action And Functions Of The Gli-related Proteins Glis 1-3Z01ES100485 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI JETTEN, ANTON M · 2002 to 2008
$2.3M
Intramural NIH HHS Z01 ES100485
6 · The paper itself

Abstract

The Krüppel-like zinc finger transcription factor, Glis3, has been associated with neonatal diabetes in humans and mice, and implicated in the regulation of pancreatic β-cell generation. However, its precise function in the development of pancreatic β-cells has not yet been elucidated. In this study, we provide evidence that Glis3 regulates Neurogenin 3 (Ngn3) through its distal promoter region. Previous studies showed that the distal region and proximal region of Ngn3 promoter contains various transcription binding sites, including binding sites for pancreatic and duodenal homeobox 1 (Pdx1), Hnf1β and Hnf6. Interestingly, putative Glis3 binding sites (Glis3BS) were found in the distal region of Ngn3 promoter close to the Hnf6 binding sites. This suggested that along with Hnf6, Glis3 may also be involved in the regulation of Ngn3 expression. This hypothesis is supported by data showing that Glis3 can bind to the Ngn3 promoter directly and activate Ngn3 transcriptional activity. Additionally, Glis3 can interact directly with Hnf6 in vitro and in vivo. The amino-terminus in Glis3 and the homeodomain of Hnf6 are critical for this interaction. These data suggest that crosstalk between Glis3 and Hnf6 may play an important role in the regulation of Ngn3 during pancreatic endocrine progenitor cell specification and development.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsHEK293 CellsHepatocyte Nuclear Factor 6Hep G2 CellsHumansInsulin-Secreting CellsIslets of LangerhansMiceNerve Tissue ProteinsPromoter Regions, GeneticProtein BindingRatsRepressor ProteinsResponse ElementsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsGlis3 protein, mouseHepatocyte Nuclear Factor 6Nerve Tissue ProteinsNeurog3 protein, mouseRepressor ProteinsTrans-Activators

Identifiers

PMID22820919
PMCPMC3465161
OpenAlexW2085165789

What OpenQuestion holds

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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.