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Bone morphogenetic protein-mediated Ventx3.2 regulates mesendoderm patterning and gut morphogenesis during Xenopus
Ravi Shankar Goutam1, Vijay Kumar2, Unjoo Lee3
1Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University, Chuncheon, Gangwon-do, 24252, Republic of Korea.
Biochemical and Biophysical Research Communications
|September 18, 2025
Summary
Ventx3.2 is crucial for gastrointestinal tract development in Xenopus laevis, linking bone morphogenetic protein (BMP) signaling to organogenesis. This study clarifies Ventx3.2
Area of Science:
- Developmental Biology
- Molecular Biology
- Genetics
Background:
- Bone morphogenetic protein (BMP) signaling is vital for vertebrate development, influencing germ layer specification and organogenesis.
- BMP signaling activates Ventx homeobox transcription factors, crucial for mesendoderm fate in Xenopus laevis.
- The specific role of Ventx3.2 in mesendoderm development and organogenesis is not well understood.
Purpose of the Study:
- To elucidate the function of Ventx3.2 in mesendoderm development and organogenesis using Xenopus laevis.
- To investigate the link between BMP signaling, Ventx3.2, and gastrointestinal tract formation.
Main Methods:
- Gain- and loss-of-function experiments in Xenopus laevis.
- Analysis of Ventx3.2 expression patterns during development.
- Gene expression profiling and morphological analyses of developing embryos.
Main Results:
- Ventx3.2 is expressed in the vegetal hemisphere during gastrulation and later in the ventral trunk and tail.
- Ventx3.2 plays a significant role in the specification and morphogenesis of mesendoderm-derived tissues, especially the gastrointestinal tract.
- Optimal Ventx3.2 expression is essential for normal gastrointestinal tract development and coiling.
Conclusions:
- Ventx3.2 is a critical downstream target of BMP signaling.
- Ventx3.2 bridges early mesendoderm patterning with gastrointestinal tract organogenesis.
- This study provides new insights into the molecular mechanisms regulating vertebrate organogenesis.

