Evidence map›Paper›PMID 31511511›Full record

ArticleNature communications2019

The WT1-like transcription factor Klumpfuss maintains lineage commitment of enterocyte progenitors in the Drosophila intestine.

Jerome Korzelius, Sina Azami, Tal Ronnen-Oron, Philipp Koch, Maik Baldauf, Elke Meier, Imilce A Rodriguez-Fernandez, Marco Groth, Pedro Sousa-Victor, Heinrich Jasper

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  6. Notch Signaling in Drosophila Tumor Models.Advances in experimental medicine and biology · 2025
    Review
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  14. Review
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  16. Article
  17. Article
  18. The MicroRNAMetabolites · 2022
    Article
  19. Article
  20. I-KCKT allows dissection-free RNA profiling of adultDevelopment (Cambridge, England) · 2021
    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

10 authors at 2 institutions in 3 countries.

Jerome KorzeliusLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany. jkorzelius@age.mpg.de.
Sina AzamiLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany.ORCID http://orcid.org/0000-0002-8702-6881
Tal Ronnen-OronBuck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA, 94945-1400, USA.
Philipp KochLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany.ORCID http://orcid.org/0000-0003-2825-7943
Maik BaldaufLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany.
Elke MeierLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany.
Imilce A Rodriguez-FernandezImmunology Discovery, Genentech, Inc., 1 DNA Way, South San Francisco, CA, 94080, USA.
Marco GrothLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany.ORCID http://orcid.org/0000-0002-9199-8990
Pedro Sousa-VictorBuck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA, 94945-1400, USA.
Heinrich JasperLeibniz Institute on Aging-Fritz Lipmann Institute (FLI), Jena, Germany. jasper.heinrich@gene.com.
Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEBuck Institute for Research on Aging · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In adult epithelial stem cell lineages, the precise differentiation of daughter cells is critical to maintain tissue homeostasis. Notch signaling controls the choice between absorptive and entero-endocrine cell differentiation in both the mammalian small intestine and the Drosophila midgut, yet how Notch promotes lineage restriction remains unclear. Here, we describe a role for the transcription factor Klumpfuss (Klu) in restricting the fate of enteroblasts (EBs) in the Drosophila intestine. Klu is induced in Notch-positive EBs and its activity restricts cell fate towards the enterocyte (EC) lineage. Transcriptomics and DamID profiling show that Klu suppresses enteroendocrine (EE) fate by repressing the action of the proneural gene Scute, which is essential for EE differentiation. Loss of Klu results in differentiation of EBs into EE cells. Our findings provide mechanistic insight into how lineage commitment in progenitor cell differentiation can be ensured downstream of initial specification cues.

Indexed as

Cell LineageAnimalsCarcinogenesisCell DifferentiationCell ProliferationDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEnterocytesIntestinesModels, BiologicalProtein BindingReceptors, NotchSignal TransductionStem CellsTranscription FactorsDNA-Binding ProteinsDrosophila ProteinsKlu protein, DrosophilaReceptors, Notchsc protein, DrosophilaTranscription Factors

Identifiers

PMID31511511
PMCPMC6739418
OpenAlexW2972785092

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.