| First Author | Zou J | Year | 2023 |
| Journal | Cell Rep | Volume | 42 |
| Issue | 1 | Pages | 112018 |
| PubMed ID | 36662623 | Mgi Jnum | J:333036 |
| Mgi Id | MGI:7432246 | Doi | 10.1016/j.celrep.2023.112018 |
| Citation | Zou J, et al. (2023) Neddylation is required for perinatal cardiac development through stimulation of metabolic maturation. Cell Rep 42(1):112018 |
| abstractText | Cardiac maturation is crucial for postnatal cardiac development and is increasingly known to be regulated by a series of transcription factors. However, post-translational mechanisms regulating this process remain unclear. Here we report the indispensable role of neddylation in cardiac maturation. Mosaic deletion of NAE1, an essential enzyme for neddylation, in neonatal hearts results in the rapid development of cardiomyopathy and heart failure. NAE1 deficiency disrupts transverse tubule formation, inhibits physiological hypertrophy, and represses fetal-to-adult isoform switching, thus culminating in cardiomyocyte immaturation. Mechanistically, we find that neddylation is needed for the perinatal metabolic transition from glycolytic to oxidative metabolism in cardiomyocytes. Further, we show that HIF1alpha is a putative neddylation target and that inhibition of neddylation accumulates HIF1alpha and impairs fatty acid utilization and bioenergetics in cardiomyocytes. Together, our data show neddylation is required for cardiomyocyte maturation through promoting oxidative metabolism in the developing heart. |
