Evidence mapPaperPMID 40326666Full record

ArticleDevelopment (Cambridge, England)2025

A function of Spalt proteins in heterochromatin organization and maintenance of genomic DNA integrity.

Cristina M Ostalé, Natalia Azpiazu, Ana Peropadre, Mercedes Martín, Mireya Ruiz-Losada, Ana López-Varea, Rebecca R Viales, Charles Girardot, Eileen E M Furlong, Jose F de Celis

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Cristina M OstaléCentro de Biología Molecular 'Severo Ochoa', Department of Tissue and Organ Homeostasis, CSIC and Universidad Autónoma de Madrid, Madrid 28049, Spain.
Natalia AzpiazuCentro de Biología Molecular 'Severo Ochoa', Department of Tissue and Organ Homeostasis, CSIC and Universidad Autónoma de Madrid, Madrid 28049, Spain.ORCID 0000-0002-1085-2341
Ana PeropadreDepartment of Biology, Universidad Autónoma de Madrid, Madrid 28049, Spain.ORCID 0000-0002-0787-9391
Mercedes MartínCentro de Biología Molecular 'Severo Ochoa', Department of Tissue and Organ Homeostasis, CSIC and Universidad Autónoma de Madrid, Madrid 28049, Spain.
Mireya Ruiz-LosadaCentro de Biología Molecular 'Severo Ochoa', Department of Tissue and Organ Homeostasis, CSIC and Universidad Autónoma de Madrid, Madrid 28049, Spain.ORCID 0000-0001-5125-4674
Ana López-VareaCentro de Biología Molecular 'Severo Ochoa', Department of Tissue and Organ Homeostasis, CSIC and Universidad Autónoma de Madrid, Madrid 28049, Spain.
Rebecca R VialesEuropean Molecular Biology Laboratory, Genome Biology Department, Heidelberg 69117, Germany.ORCID 0000-0003-3739-7438
Charles GirardotEuropean Molecular Biology Laboratory, Genome Biology Department, Heidelberg 69117, Germany.ORCID 0000-0003-4301-3920
Eileen E M FurlongEuropean Molecular Biology Laboratory, Genome Biology Department, Heidelberg 69117, Germany.
Jose F de CelisCentro de Biología Molecular 'Severo Ochoa', Department of Tissue and Organ Homeostasis, CSIC and Universidad Autónoma de Madrid, Madrid 28049, Spain.ORCID 0000-0003-4808-9844

Funding

Consejo Superior de Investigaciones CientíficasDeutsche Forschungsgemeinschaft DFG-SPP 2202European Research Council DeCRyPT (787611)Secretaría de Estado de Investigación, Desarrollo e Innovación PID2022-141894OB-C21Spanish National Plan for Scientific and Technical Research and Innovation PID2022-141894OB-C21
6 · The paper itself

Abstract

The conserved Spalt proteins regulate gene expression and cell fate choices during multicellular development, generally acting as transcriptional repressors in different gene regulatory networks. In addition to their roles as DNA sequence-specific transcription factors, Spalt proteins show a consistent localization to heterochromatic regions. Vertebrate Spalt-like proteins can act through the nucleosome remodeling and deacetylase complex to promote closing of open chromatin domains, but their activities also rely on interactions with DNA methyltransferases or with the lysine-specific histone demethylase LSD1, suggesting that they participate in multiple regulatory mechanisms. Here, we describe several consequences of loss of Spalt function in Drosophila cells, including changes in chromatin accessibility, generation of DNA damage, alterations in the localization of chromosomes within the nucleus in the salivary glands and misexpression of transposable elements. We suggest that these effects are related to roles of Spalt proteins in the regulation of heterochromatin formation and chromatin organization. We propose that Drosophila Spalt proteins have two complementary functions, acting as sequence-specific transcriptional repressors on specific target genes and regulating more global gene silencing through the generation or maintenance of heterochromatic domains.

Indexed as

DNADrosophila ProteinsHeterochromatinAnimalsDNA DamageDNA Transposable ElementsDrosophilaDrosophila melanogasterRepressor ProteinsSalivary GlandsTranscription FactorsDNADNA Transposable ElementsDrosophila ProteinsHeterochromatinRepressor ProteinsTranscription FactorsDrosophilaGene expressionHeterochromatinNuclear laminaNucleolusSpalt proteins

Identifiers

PMID40326666
PMCPMC12091872

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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 Socratic graph.