Evidence map›Paper›PMID 9315659›Full record

ArticleMolecular and cellular biology1997

Hepatocyte nuclear factor 3beta is involved in pancreatic beta-cell-specific transcription of the pdx-1 gene.

K L Wu, M Gannon, M Peshavaria, M F Offield, E Henderson, M Ray, A Marks, L W Gamer, C V Wright, R Stein

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
10.3field-weighted citation impact, top 1% 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

93 citing papers in PubMed, 255 citations in OpenAlex.

  1. Review
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  9. CRISPR/Cas9Frontiers in endocrinology · 2021
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  12. Article
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  14. Article
  15. Article
  16. Article
  17. Pancreatic regulation of glucose homeostasis.Experimental & molecular medicine · 2016
    Review
  18. Review
  19. Article
  20. Review

33 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

10 authors at 2 institutions in 2 countries.

K L WuDepartment of Molecular Physiology and Biophysics, Vanderbilt Medical Center, Nashville, Tennessee 37232, USA.
M Gannon
M Peshavaria
M F Offield
E Henderson
M Ray
A Marks
L W Gamer
C V Wright
R Stein
Vanderbilt University Medical Center · USInstitute of Molecular Biology and Biophysics · RU

Funding

PDX-1,A TRANSCRIPTIONAL ACTIVATOR OF THE INSULIN GENER01DK050203 · NIDDK · VANDERBILT UNIVERSITY · PI BASS, JOSEPH, STEIN, ROLAND W · 1995 to 2020
$6.8M
HOMEOBOX GENES IN VERTEBRATE EMBRYONIC ENDODERMR01HD028062 · NICHD · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V. · 1991 to 1995
–
NICHD NIH HHS R01 HD 28062NIDDK NIH HHS DK42502NIDDK NIH HHS R01 DK50203
6 · The paper itself

Abstract

The mammalian homeobox gene pdx-1 is expressed in pluripotent precursor cells in the dorsal and ventral pancreatic bud and duodenal endoderm, which will produce the pancreas and the rostral duodenum. In the adult, pdr-1 is expressed principally within insulin-secreting pancreatic islet beta cells and cells of the duodenal epithelium. Our objective in this study was to localize sequences within the mouse pdx-1 gene mediating selective expression within the islet. Studies of transgenic mice in which a genomic fragment of the mouse pdx-1 gene from kb -4.5 to +8.2 was used to drive a beta-galactosidase reporter showed that the control sequences sufficient for appropriate developmental and adult specific expression were contained within this region. Three nuclease-hypersensitive sites, located between bp -2560 and -1880 (site 1), bp -1330 and -800 (site 2), and bp -260 and +180 (site 3), were identified within the 5'-flanking region of the endogenous pdx-1 gene. Pancreatic beta-cell-specific expression was shown to be controlled by sequences within site 1 from an analysis of the expression pattern of various pdr-1-herpes simplex virus thymidine kinase promoter expression constructs in transfected beta-cell and non-beta-cell lines. Furthermore, we also established that this region was important in vivo by demonstrating that expression from a site 1-driven beta-galactosidase reporter construct was directed to islet beta-cells in transgenic mice. The activity of the site 1-driven constructs was reduced substantially in beta-cell lines by mutating a hepatocyte nuclear factor 3 (HNF3)-like site located between nucleotides -2007 and -1996. Gel shift analysis indicated that HNF3beta present in islet beta cells binds to this element. Immunohistochemical studies revealed that HNF3beta was present within the nuclei of almost all islet beta cells and subsets of pancreatic acinar cells. Together, these results suggest that HNF3beta, a key regulator of endodermal cell lineage development, plays an essential role in the cell-type-specific transcription of the pdx-1 gene in the pancreas.

Indexed as

Transcription FactorsAnimalsCells, CulturedDNADNA-Binding ProteinsGene Expression Regulation, DevelopmentalHepatocyte Nuclear Factor 3-betaHomeodomain ProteinsHumansIslets of LangerhansMiceMice, Inbred ICRMice, TransgenicNuclear ProteinsOrgan SpecificityPancreasDNADNA-Binding ProteinsFOXA2 protein, humanFoxa2 protein, mouseHepatocyte Nuclear Factor 3-betaHomeodomain ProteinsNuclear Proteinspancreatic and duodenal homeobox 1 proteinRecombinant Fusion ProteinsRNA, MessengerTrans-ActivatorsTranscription Factors

Identifiers

PMID9315659
PMCPMC232449
OpenAlexW1992517228

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.