Evidence map›Paper›PMID 39962064›Full record

ArticleNature communications2025

BMP signaling promotes zebrafish heart regeneration via alleviation of replication stress.

Mohankrishna Dalvoy Vasudevarao, Denise Posadas Pena, Michaela Ihle, Chiara Bongiovanni, Pallab Maity, Dominik Geissler, Hossein Falah Mohammadi, Melanie Rall-Scharpf, Julian Niemann, Mathilda T M Mommersteeg and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

20 authors.

Mohankrishna Dalvoy Vasudevarao *Institute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Denise Posadas Pena *Institute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Michaela IhleDepartment of Obstetrics and Gynecology, Ulm University, Prittwitzstraße 43, 89075, Ulm, Germany.
Chiara BongiovanniDepartment of Medical and Surgical Sciences, University of Bologna, via Massarenti 9, 40138, Bologna, Italy.
Pallab MaityDepartment of Dermatology and Allergic Diseases, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0001-9769-3533
Dominik GeisslerInstitute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.ORCID http://orcid.org/0009-0001-6839-7046
Hossein Falah MohammadiInstitute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Melanie Rall-ScharpfDepartment of Obstetrics and Gynecology, Ulm University, Prittwitzstraße 43, 89075, Ulm, Germany.ORCID http://orcid.org/0000-0003-2991-5223
Julian NiemannInstitute of Molecular Medicine, Ulm University, Meyerhofstrasse N27, 89081, Ulm, Germany.
Mathilda T M MommersteegDepartment of Physiology, Anatomy and Genetics, University of Oxford, South Parks Road, Oxford, OX1 3PT, United Kingdom.ORCID http://orcid.org/0000-0001-6624-3038
Simone RedaelliInstitute of Biomedical Ethics and History of Medicine, University of Zurich, Winterthurerstrasse 30, 8006, Zurich, Switzerland.
Kathrin HappInstitute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Chi-Chung WuInstitute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Arica BeisawInstitute of Experimental Cardiology, Heidelberg University, Im Neuenheimer Feld 669, 69120, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-6658-6978
Karin Scharffetter-KochanekDepartment of Dermatology and Allergic Diseases, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0002-9655-685X
Gabriele D'UvaDepartment of Medical and Surgical Sciences, University of Bologna, via Massarenti 9, 40138, Bologna, Italy.
Mona Malek MohammadiInstitute of Physiology I, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.ORCID http://orcid.org/0000-0001-8410-7865
Lisa WiesmüllerDepartment of Obstetrics and Gynecology, Ulm University, Prittwitzstraße 43, 89075, Ulm, Germany.ORCID http://orcid.org/0000-0002-2397-5041
Hartmut GeigerInstitute of Molecular Medicine, Ulm University, Meyerhofstrasse N27, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0002-5794-5430
Gilbert WeidingerInstitute of Biochemistry and Molecular Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany. gilbert.weidinger@uni-ulm.de.ORCID http://orcid.org/0000-0003-3599-6760

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In contrast to mammals, adult zebrafish achieve complete heart regeneration via proliferation of cardiomyocytes. Surprisingly, we found that regenerating cardiomyocytes experience DNA replication stress, which represents one reason for declining tissue regeneration during aging in mammals. Pharmacological inhibition of ATM and ATR kinases revealed that DNA damage response signaling is essential for zebrafish heart regeneration. Manipulation of Bone Morphogenetic Protein (BMP)-Smad signaling using transgenics and mutants showed that BMP signaling alleviates cardiomyocyte replication stress. BMP signaling also rescues neonatal mouse cardiomyocytes, human fibroblasts and human hematopoietic stem and progenitor cells (HSPCs) from replication stress. DNA fiber spreading assays indicate that BMP signaling facilitates re-start of replication forks after replication stress-induced stalling. Our results identify the ability to overcome replication stress as key factor for the elevated zebrafish heart regeneration capacity and reveal a conserved role for BMP signaling in promotion of stress-free DNA replication.

Indexed as

Bone Morphogenetic ProteinsDNA ReplicationHeartRegenerationSignal TransductionZebrafishZebrafish ProteinsAnimalsAnimals, Genetically ModifiedAtaxia Telangiectasia Mutated ProteinsCell ProliferationDNA DamageFibroblastsHematopoietic Stem CellsHumansMiceAtaxia Telangiectasia Mutated ProteinsBone Morphogenetic ProteinsSmad ProteinsZebrafish Proteins

Identifiers

PMID39962064
PMCPMC11832743

What Socratic 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 Socratic graph.