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- W4313646521 abstract "Fibrodysplasia ossificans progressiva (FOP), a rare disease characterized by progressive heterotopic ossification of muscle and connective tissues, is caused by autosomal dominant activating mutations in the type I receptor, ACVR1/ALK2. The classic human FOP variant, ACVR1R206H , shows increased bone morphogenetic protein (BMP) signaling and activation by activins.Here, we performed in vivo functional characterization of human ACVR1R206H and orthologous zebrafish Acvr1lR203H using early embryonic zebrafish dorsoventral patterning as a phenotypic readout for receptor activity. Our results showed that human ACVR1R206H and zebrafish Acvr1lR203H exhibit functional differences in early embryonic zebrafish, and that human ACVR1R206H retained its signaling activity in the absence of a ligand-binding domain (LBD). We also showed, for the first time, that zebrafish Acvr2ba/Acvr2bb receptors are required for human ACVR1R206H signaling in early embryonic zebrafish.Together, these data provide new insight into ACVR1R206H signaling pathways that may facilitate the design of new and effective therapies for FOP patients." @default.
- W4313646521 created "2023-01-07" @default.
- W4313646521 creator A5002571994 @default.
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- W4313646521 creator A5082117794 @default.
- W4313646521 date "2023-01-26" @default.
- W4313646521 modified "2023-09-26" @default.
- W4313646521 title "Functional comparison of human <scp>ACVR1</scp> and zebrafish Acvr1l <scp>FOP</scp>‐associated variants in embryonic zebrafish" @default.
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- W4313646521 doi "https://doi.org/10.1002/dvdy.566" @default.
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- W4313646521 hasPublicationYear "2023" @default.
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