PUBLICATION

Ddx61-enriched condensates refine heart regeneration programs

Authors
Pronobis, M.I., DeLuca, S., Lee, S., Garcia, L., Ou, J., Bursac, N., Poss, K.D.
ID
ZDB-PUB-251010-8
Date
2025
Source
Nature communications   16: 89928992 (Journal)
Registered Authors
Poss, Kenneth D., Pronobis, Mira
Keywords
none
Datasets
GEO:GSE246577
MeSH Terms
  • Animals
  • Cell Proliferation
  • Cells, Cultured
  • DEAD-box RNA Helicases*/genetics
  • DEAD-box RNA Helicases*/metabolism
  • Heart*/physiology
  • Humans
  • Intercellular Signaling Peptides and Proteins/genetics
  • Intercellular Signaling Peptides and Proteins/metabolism
  • Mice
  • Myocytes, Cardiac*/cytology
  • Myocytes, Cardiac*/metabolism
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Regeneration*/genetics
  • Regeneration*/physiology
  • Zebrafish/genetics
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/metabolism
PubMed
41068075 Full text @ Nat. Commun.
Abstract
Gene regulatory mechanisms that underlie tissue regeneration have been largely studied at the level of transcription. Here, proximity labeling methods identify increased presence of the RNA helicase and P-body marker Ddx61 in adult zebrafish cardiomyocytes induced to divide by injury or mitogens. Ddx61 molecules form complex condensates in cardiomyocytes during cardiogenic settings in zebrafish, developing mice, and cultured human cells. ddx61 mutations disrupt cardiomyocyte proliferation and heart regeneration indices in adult zebrafish, and DDX6 knockdown reduces proliferation of cultured human cardiomyocytes. During heart regeneration, Ddx61 associates with and is required to restrain expression of mRNA encoding Chordin, a secreted BMP inhibitor that impedes regeneration if present at high levels. Our experiments indicate that mRNA sorting by context-dependent condensates can impact tissue regenerative capacity.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping