Year: 2020
Type: article
Abstract: β-catenin has been widely studied in many animal and organ systems across evolution, and gain or loss of function has been linked to a number of human diseases. Yet fundamental knowledge regarding its protein expression and localization remains poorly described. Thus, we sought to define whether there was a temporal and cell-specific regulation of β-catenin activities that correlate with distinct cardiac morphological events. Our findings indicate that activated nuclear β-catenin is primarily evident early in gestation. As development proceeds, nuclear β-catenin is down-regulated and becomes restricted to the membrane in a subset of cardiac progenitor cells. After birth, little β-catenin is detected in the heart. The co-expression of β-catenin with its main transcriptional co-factor, Lef1, revealed that Lef1 and β-catenin expression domains do not extensively overlap in the cardiac valves. These data indicate mutually exclusive roles for Lef1 and β-catenin in most cardiac cell types during development. Additionally, these data indicate diverse functions for β-catenin within the nucleus and membrane depending on cell type and gestational timing. Cardiovascular studies should take into careful consideration both nuclear and membrane β-catenin functions and their potential contributions to cardiac development and disease.
DOI: 10.3390/jcdd7030031
Institution: Medical University of South Carolina
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $1,056
Awards: G1250730630, G150219179, G2201271997, G2591975879, G2934836127, G3207227387, G3255071938, G350062807, G3777309589, G4109466933, G4483406021, G5173863161, G547628071, G5514089648, G6106915579, EXTRAMURAL RESEARCH FACILITIES CONSTRUCTION, G6781035106, G6842549510, G7556331398, Dzip1 and Mitral Valve Prolapse, G8971373830
OpenAlex ID: W3049348349
