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Updated: Apr 22, 2026

En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos
Published on: July 27, 2022
BAF200 is required for heart morphogenesis and coronary artery development
Lingjuan He1, Xueying Tian1, Hui Zhang1
1Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Graduate School of the Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.
The PBAF complex subunit BAF200 is crucial for embryonic development. BAF200 deficiency in mice leads to severe cardiac defects and impaired coronary artery formation, highlighting its role in heart morphogenesis.
Area of Science:
- Molecular Biology
- Developmental Biology
- Genetics
Background:
- ATP-dependent SWI/SNF chromatin remodeling complexes are vital for development and disease.
- Mammalian SWI/SNF complexes exist as BAF and PBAF subcomplexes.
- ARID2 (BAF200) is a subunit of the PBAF complex, but its in vivo function is unknown.
Purpose of the Study:
- To investigate the in vivo function of BAF200 in embryogenesis and organ development.
Main Methods:
- Generation of BAF200 mutant mice.
- Phenotypic analysis of mutant embryos, focusing on cardiac development and coronary artery formation.
Main Results:
- BAF200 mutant mice are embryonic lethal.
- Mutant embryos display significant cardiac abnormalities, including thin myocardium and septal defects.
- Reduced intramyocardial coronary arteries were observed in BAF200 mutants, indicating impaired angiogenesis.
Conclusions:
- BAF200 is essential for embryonic survival and proper heart development.
- The PBAF complex plays a critical role in heart morphogenesis and coronary artery angiogenesis.
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