PUBLICATION
The Zebrafish miR-183 Family Regulates Endoderm Convergence and Heart Development via S1Pr2 Signaling Pathway
- Authors
- Zeng, T., Liu, L., Lv, J., Xie, H., Shi, Q., Tao, G., Zheng, X., Zhu, L., Xiong, L., Xie, H.
- ID
- ZDB-PUB-251029-27
- Date
- 2025
- Source
- Biomolecules 15: (Journal)
- Registered Authors
- Xie, Huaping, Xiong, Lei, Zeng, Ting
- Keywords
- S1Pr2, cardia bifida, cardiac precursor cells, endoderm, zebrafish
- MeSH Terms
-
- Animals
- Animals, Genetically Modified
- Endoderm*/embryology
- Endoderm*/metabolism
- Gene Expression Regulation, Developmental
- Heart*/embryology
- MicroRNAs*/genetics
- MicroRNAs*/metabolism
- Organogenesis/genetics
- Signal Transduction
- Sphingosine-1-Phosphate Receptors*/genetics
- Sphingosine-1-Phosphate Receptors*/metabolism
- Zebrafish*/embryology
- Zebrafish*/genetics
- Zebrafish*/metabolism
- Zebrafish Proteins*/genetics
- Zebrafish Proteins*/metabolism
- PubMed
- 41154662 Full text @ Biomolecules
Citation
Zeng, T., Liu, L., Lv, J., Xie, H., Shi, Q., Tao, G., Zheng, X., Zhu, L., Xiong, L., Xie, H. (2025) The Zebrafish miR-183 Family Regulates Endoderm Convergence and Heart Development via S1Pr2 Signaling Pathway. Biomolecules. 15:.
Abstract
MicroRNA (miRNA), as a key post-transcriptional regulatory factor, plays a crucial role in embryonic development. The coordination of endoderm cell convergence and cardiac precursor cell (CPC) migration is critical for cardiac tube fusion. Defects in endoderm can impair the normal migration of CPCs towards the midline, leading to cardia bifida. Although the role of the microRNA-183 family (miR-183, miR-96 and miR-182) in cardiovascular diseases has been reported, the mechanism by which they regulate early heart development remains unclear. In this study, we used zebrafish as a model to elucidate the roles of the microRNA-183 family in early heart development. miRNA mimics were injected into Tg (cmlc2: eGFP) and Tg (sox17: eGFP) transgenic embryos to overexpress the miR-183 family. The results showed that, at 36 hpf, single or co-injection of miR-183/96/182 mimics caused defects in endoderm convergence, with a hole in the endoderm, and a significant down-regulation of the endoderm marker gene sox32. Additionally, embryos with single or co-injection of miR-183/96/182 mimics exhibited cardia bifida and tail blisters, with significantly down-regulated expression levels of genes related to heart development, including cmlc2, vmhc, amhc, nppa, gata4, gata5, nkx2.5, bmp2b, and bmp4. The phenotype caused by overexpression of the miR-183 family is highly consistent with loss of the sphingosine 1-phosphate receptor S1Pr2. Bioinformatics analysis result found that miR-183 can bind to 3'-UTR of the s1pr2 to regulate its expression; overexpression of miR-183 led to a significant decrease in the expression of the s1pr2 gene. Dual luciferase assay results suggest that s1pr2 is a bona fide target of miR-183. In summary, the miR-183 family regulates endoderm convergence and cardiac precursor cell migration via the S1Pr2 signaling pathway. This study reveals that the miR-183 family is a key regulatory factor in endoderm convergence and cardiac precursor cell migration during the early zebrafish development, elucidating the molecular mechanisms underlying early cardiac precursor cell and endoderm cell movement.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping