Evidence map›Paper›PMID 20627934›Full record

ArticleDiabetes2010

MafA and MafB regulate genes critical to beta-cells in a unique temporal manner.

Isabella Artner, Yan Hang, Magdalena Mazur, Tsunehiko Yamamoto, Min Guo, Jill Lindner, Mark A Magnuson, Roland Stein

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 160 papers.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed
14.5field-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

160 citing papers in PubMed, 242 citations in OpenAlex.

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  19. MafB MaintainsMolecular and cellular biology · 2022
    Article
  20. Review

100 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

8 authors at 2 institutions in 2 countries.

Isabella ArtnerDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee, USA. isabella.artner@med.lu.se
Yan Hang
Magdalena Mazur
Tsunehiko Yamamoto
Min Guo
Jill Lindner
Mark A Magnuson
Roland Stein
Vanderbilt University · USLund University · SE

Funding

Coordinating Center for Beta Cell Biology ConsortiumU01DK072473 · NIDDK · VANDERBILT UNIVERSITY · PI MAGNUSON, MARK A · 2005 to 2014
$61.0M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI POWERS, ALVIN C · 1986 to 2011
$28.1M
Ketosis, Vascular Inflammation and Its Therapy in Type 1 Diabetic PatientsR01DK072433 · NIDDK · LOUISIANA STATE UNIV HSC SHREVEPORT · PI JAIN, SUSHIL K · 2007 to 2010
$1.3M
TRANSGENIC MICE COREP01DK042502 · NIDDK · VANDERBILT UNIVERSITY · PI MAGNUSON, MARK A · 1990 to 2000
$994k
NIDDK NIH HHS DK-72433NIDDK NIH HHS P01 DK042502NIDDK NIH HHS P01 DK-42502NIDDK NIH HHS P60 DK020593NIDDK NIH HHS P60 DK-20593NIDDK NIH HHS R01 DK072433NIDDK NIH HHS U01 DK072473
6 · The paper itself

Abstract

objectiveSeveral transcription factors are essential to pancreatic islet β-cell development, proliferation, and activity, including MafA and MafB. However, MafA and MafB are distinct from others in regard to temporal and islet cell expression pattern, with β-cells affected by MafB only during development and exclusively by MafA in the adult. Our aim was to define the functional relationship between these closely related activators to the β-cell. RESEARCH DESIGN AND

methodsThe distribution of MafA and MafB in the β-cell population was determined immunohistochemically at various developmental and perinatal stages in mice. To identify genes regulated by MafB, microarray profiling was performed on wild-type and MafB(-/-) pancreata at embryonic day 18.5, with candidates evaluated by quantitative RT-PCR and in situ hybridization. The potential role of MafA in the expression of verified targets was next analyzed in adult islets of a pancreas-wide MafA mutant (termed MafA(ΔPanc)).

resultsMafB was produced in a larger fraction of β-cells than MafA during development and found to regulate potential effectors of glucose sensing, hormone processing, vesicle formation, and insulin secretion. Notably, expression from many of these genes was compromised in MafA(ΔPanc) islets, suggesting that MafA is required to sustain expression in adults.

conclusionsOur results provide insight into the sequential manner by which MafA and MafB regulate islet β-cell formation and maturation.

Indexed as

AgingAnimalsEmbryonic DevelopmentGene Expression Regulation, DevelopmentalGlucagonGlucose-6-PhosphataseInsulinInsulin-Secreting CellsMafB Transcription FactorMaf Transcription Factors, LargeMiceOligonucleotide Array Sequence AnalysisProteinsRetinol-Binding Proteins, PlasmaReverse Transcriptase Polymerase Chain ReactionRNAG6pc2 protein, mouseGlucagonGlucose-6-PhosphataseInsulinMafa protein, mouseMafb protein, mouseMafB Transcription FactorMaf Transcription Factors, LargeProteinsRbp4 protein, mouseRetinol-Binding Proteins, PlasmaRNARNA, Messenger

Identifiers

PMID20627934
PMCPMC3279542
OpenAlexW2103306919

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.