Evidence map›Paper›PMID 42830491›Full record

ArticleDevelopment, growth & differentiation2026

Ptbp1 Condensates With Phase Separation-Like Features in Cardiomyocyte Nuclei Regulate Splicing of Proliferative Genes in Neonatal Cardiomyocytes.

Tai Sada, Akane Sakaguchi, Yoichi Shinkai, Reiko Nakagawa, Chiharu Tanegashima, Mitsutaka Kadota, Takefumi Kondo, Wataru Kimura

Abstract read
In one paragraph

Article in Development, growth & differentiation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

8 authors.

Tai SadaLaboratory for Heart Regeneration, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.ORCID https://orcid.org/0009-0000-3087-4890
Akane SakaguchiLaboratory for Heart Regeneration, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.ORCID https://orcid.org/0000-0003-1449-0840
Yoichi ShinkaiCellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan.ORCID https://orcid.org/0000-0001-8366-6278
Reiko NakagawaMass Spectrometry Analysis Team, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.ORCID https://orcid.org/0000-0002-6178-2945
Chiharu TanegashimaGenomics Research and Analysis Support Team, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.
Mitsutaka KadotaGenomics Research and Analysis Support Team, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.ORCID https://orcid.org/0000-0002-1674-6697
Takefumi KondoGenomics Research and Analysis Support Team, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.ORCID https://orcid.org/0000-0001-8127-1141
Wataru KimuraLaboratory for Heart Regeneration, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.ORCID https://orcid.org/0000-0001-6548-6353

Funding

Bristol-Myers SquibbHoansha FoundationJapan Agency for Medical Research and DevelopmentJapanese Circulation SocietyJapanese Society of Gout and Uric & Nucleic AcidsJapan Science and Technology Agency JPMJFR210OJapan Science and Technology Agency JPMJSP2138Japan Society for the Promotion of Science 17H05083Japan Society for the Promotion of Science 19K22629Japan Society for the Promotion of Science 20H03680Japan Society for the Promotion of Science 21K18273Japan Society for the Promotion of Science 23H02913Mitsubishi FoundationMiyata Cardiac Research Promotion FoundationMochida Memorial Foundation for Medical and Pharmaceutical ResearchNaito FoundationPrincess Takamatsu Cancer Research FundRIKENSenri Life Science FoundationTakeda Science FoundationToray Science FoundationUehara Memorial FoundationYakult Bio-Science Foundation
6 · The paper itself

Abstract

Cardiovascular diseases remain the leading cause of morbidity and mortality worldwide; however, effective clinical therapies that achieve myocardial regeneration are still lacking, underscoring the urgent need for novel therapeutic strategies. In this study, we identified an RNA-binding protein Ptbp1, a key component of RNA metabolism, as a critical regulator of cardiomyocyte proliferation via the formation of biomolecular condensates. We found that Ptbp1 exhibits granule-like structures in cardiomyocyte nuclei during fetal to early postnatal stages. These Ptbp1 foci are phase-separated liquid droplets formed via its multivalent RNA binding domains. Functional analyses revealed that Ptbp1 is essential for cardiomyocyte proliferation in neonatal mouse primary culture assays. Furthermore, proximity labeling using a primary antibody-based approach combined with RIP-seq in highly purified cardiomyocyte populations demonstrated that these condensates are enriched with multiple proliferation-associated factors. Our findings identify a novel phase-separated condensate in cardiomyocytes and provide a new potential therapeutic target for cardiac regeneration.

Indexed as

Cell NucleusCell ProliferationHeterogeneous-Nuclear RibonucleoproteinsMyocytes, CardiacPolypyrimidine Tract-Binding ProteinRNA SplicingAnimalsAnimals, NewbornCells, CulturedMicePhase SeparationHeterogeneous-Nuclear RibonucleoproteinsPolypyrimidine Tract-Binding ProteinPtbp1 protein, mousecardiomyocyte proliferationHnrnph1Matr3phase separationPNCPtbp1RNA binding proteins

Identifiers

PMID42830491
PMCPMC13635472

What OpenQuestion holds

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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 OpenQuestion graph.