Evidence map›Paper›PMID 16580660›Full record

ArticleDevelopmental biology2006

A switch from MafB to MafA expression accompanies differentiation to pancreatic beta-cells.

Wataru Nishimura, Takuma Kondo, Therese Salameh, Ilham El Khattabi, Rikke Dodge, Susan Bonner-Weir, Arun Sharma

Abstract read
In one paragraph

Article in Developmental biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 175 papers.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed
18.5field-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

175 citing papers in PubMed, 294 citations in OpenAlex.

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  20. MafB MaintainsMolecular and cellular biology · 2022
    Article

115 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

7 authors at 1 institution in 1 country.

Wataru NishimuraSection of Islet Transplantation and Cell Biology, Joslin Diabetes Center, Boston, MA 02215, USA.
Takuma Kondo
Therese Salameh
Ilham El Khattabi
Rikke Dodge
Susan Bonner-Weir
Arun Sharma
Joslin Diabetes Center · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 1986 to 2026
$50.5M
RIPE3b1, An Important Insulin Gene Transcription FactorR01DK060127 · NIDDK · JOSLIN DIABETES CENTER · PI SHARMA, ARUN J · 2003 to 2010
$2.5M
NIDDK NIH HHS DK060127NIDDK NIH HHS DK-36836NIDDK NIH HHS P30 DK036836NIDDK NIH HHS R01 DK060127
6 · The paper itself

Abstract

Major insulin gene transcription factors, such as PDX-1 or NeuroD1, have equally important roles in pancreatic development and the differentiation of pancreatic endocrine cells. Previously, we identified and cloned another critical insulin gene transcription factor MafA (RIPE3b1) and reported that other Maf factors were expressed in pancreatic endocrine cells. Maf factors are important regulators of cellular differentiation; to understand their role in differentiation of pancreatic endocrine cells, we analyzed the expression pattern of large-Maf factors in the pancreas of embryonic and adult mice. Ectopically expressed large-Maf factors, MafA, MafB, or cMaf, induced expression from insulin and glucagon reporter constructs, demonstrating a redundancy in their function. Yet in adult pancreas, cMaf was expressed in both alpha- and beta-cells, and MafA and MafB showed selective expression in the beta- and alpha-cells, respectively. Interestingly, during embryonic development, a significant proportion of MafB-expressing cells also expressed insulin. In embryos, MafB is expressed before MafA, and our results suggest that the differentiation of beta-cells proceeds through a MafB+ MafA- Ins+ intermediate cell to MafB- MafA+ Ins+ cells. Furthermore, the MafB to MafA transition follows induction of PDX-1 expression (Pdx-1(high)) in MafB+ Ins+ cells. We suggest that MafB may have a dual role in regulating embryonic differentiation of both beta- and alpha-cells while MafA may regulate replication/survival and function of beta-cells after birth. Thus, this redundancy in the function and expression of the large-Maf factors may explain the normal islet morphology observed in the MafA knockout mice at birth.

Indexed as

AnimalsBase SequenceCell DifferentiationCell ProliferationFemaleGene Expression Regulation, DevelopmentalGenes, ReporterGlucagonHeLa CellsHumansInsulinIslets of LangerhansMafB Transcription FactorMaf Transcription Factors, LargeMiceMice, Inbred C57BLGlucagonInsulinMafa protein, mouseMafb protein, mouseMafB Transcription FactorMaf Transcription Factors, LargeRNA, Messenger

Identifiers

PMID16580660
PMCPMC2390934
OpenAlexW2139943786

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.