Presenter: Maithri Sarangam
Mentor: Kryn Stankunas
AM Poster Presentation
Poster 43
Congenital heart diseases are one of the most common types of birth defects. Studying the development of this complex organ may provide insight into the causes of such defects. It has been shown that chromatin remodeling complexes play a role in directing developmental processes. They affect expression of genes by modifying chromatin, the DNA-protein complex in the nucleus. One particular chromatin remodeling complex, the BAF complex, has been shown to be important in heart development. We believe the BAF complex is required during the remodeling and elongation phase of aortic valve development. The aortic valve controls blood flow from the heart through the aorta. We used mouse models and complex genetic techniques to study the role of the BAF complex in mammalian heart valve development. Using a crelox system, we induced a loss of function of the BAF complex in endocardial cells, which make up the lining the heart, by knocking out Brg1, the key ATP-ase required for the complex to function. We then used various histological and immunofluorescence stains to study the resulting phenotype at different time points during the elongation and remodeling phase. The aortic valve phenotypes in the mutant embryos deviated from that of their wild type litter-mates, suggesting that the BAF complex does have a role in this phase of valve development.