Why the study?
Endothelin convert enzyme-1 (ECE-1) plays a significant role in cardiovascular development, but the functions of its four isoforms remain unclear.
Does the expression of human ECE-1 isoforms enhance Bax-induced apoptosis in a yeast model?
Does the expression of human ECE-1 isoforms enhance Bax-induced apoptosis in a yeast model?
Human ECE-1 isoforms, particularly ECE-1c, enhance Bax-induced apoptosis in a yeast model, suggesting a potential mechanism underlying congenital heart disease.
Yeast model for ECE-1 isoforms in apoptosis may aid CHD research; leaves open clinical translation.
Endothelin convert enzyme-1(ECE-1) plays a significant role in cardiovascular development including four isoforms with unclear function. Therefore, we are interested in studying the function of ECE-1 isoforms through mitochondria due to the high correlation between congenital heart disease (CHD) and apoptosis. Since the expression of human Bax and Bcl-xL in budding yeast ( Saccharomyces cerevisiae ) results in similar effects in mammalian cells, a yeast system was generated for mimicking human Bax-induced apoptosis and the expression of human ECE-1 isoforms was involved. The correlation between Bax-induced growth defect and the candidates of apoptosis via mitochondrial pathway was preliminarily investigated in this system. Furthermore, the phenotypes of ECE-1 isoforms have been identified through yeast growth defect. Individual ECE-1 isoform does not affect yeast growth but act as enhancers for the Bax-induced growth defect. ECE-1c is the strongest enhancer that affect the expression of candidates of outer membrane translocases. This study indicates that ECE-1 might play an important role in inducing apoptosis and we speculate these findings are possible to provide new perspectives with clarifying the mechanism of CHD.
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Huang et al. (2023) studied this question.
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