Ddx3xa mutations drive cardiac defects in a zebrafish model via dysregulation of wnt/β-catenin signaling

This study provides the first evidence that <i>ddx3xa</i> regulates cardiac morphogenesis by modulating the Wnt/β-catenin signaling pathway, offering direct experimental insight into the mechanisms underlying cardiac comorbidities in DDX3X syndrome. It also highlights the unique value of the zebrafish model for dissecting conserved pathogenic pathways and exploring targeted therapeutic strategies.

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Publication Details

Journal
Frontiers in Molecular Biosciences
Published
2025-11-27
DOI
https://doi.org/10.3389/fmolb.2025.1689202
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
0.00

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article

Ddx3xa mutations drive cardiac defects in a zebrafish model via dysregulation of wnt/β-catenin signaling

Lin Mei, Xiongwei Fan, Yi Kang, Ping Zhu et al.
Frontiers in Molecular Biosciences
Congenital heart defects research
article

Ddx3xa mutations drive cardiac defects in a zebrafish model via dysregulation of wnt/β-catenin signaling

Lin Mei, Xiongwei Fan, Yi Kang, Ping Zhu, Fang Li, Yu Chen, Haochen Wang, Yongqing Li, Yingze Zhang, Xueting Yang, Xiaoyan Cai, Zhigang Jiang, Xiushan Wu, Wuzhou Yuan, Yuequn Wang, Z. Jiao
article en

Abstract

This study provides the first evidence that <i>ddx3xa</i> regulates cardiac morphogenesis by modulating the Wnt/β-catenin signaling pathway, offering direct experimental insight into the mechanisms underlying cardiac comorbidities in DDX3X syndrome. It also highlights the unique value of the zebrafish model for dissecting conserved pathogenic pathways and exploring targeted therapeutic strategies.

Frontiers in Molecular BiosciencesVol. 12
Hunan Normal University (CN), Guangdong Academy of Medical Sciences (CN), Guangdong Provincial People's Hospital (CN), Southern Medical University (CN)
National Natural Science Foundation of China, Guangdong Special Support Plan
Openalex Percentile: Top 67%
Congenital heart defects research
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