Long-Chain Acyl-CoA Synthetase 4A Regulates Smad Activity and Dorsoventral Patterning in the Zebrafish Embryo
- Authors
- Miyares, R.L., Stein, C., Renisch, B., Anderson, J.L., Hammerschmidt, M., and Farber, S.A.
- ID
- ZDB-PUB-140210-23
- Date
- 2013
- Source
- Developmental Cell 27(6): 635-647 (Journal)
- Registered Authors
- Anderson, Jennifer, Anderson, Jennifer, Farber, Steven, Hammerschmidt, Matthias, Miyares, Rosa, Renisch, Bjoern, Stein, Cornelia
- Keywords
- none
- MeSH Terms
-
- Animals
- Transforming Growth Factor beta/genetics
- Transforming Growth Factor beta/metabolism
- Proto-Oncogene Proteins c-akt/genetics
- Proto-Oncogene Proteins c-akt/metabolism
- Signal Transduction
- In Situ Hybridization
- Acyl Coenzyme A/metabolism
- Phosphorylation
- Phenotype
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- p38 Mitogen-Activated Protein Kinases/genetics
- p38 Mitogen-Activated Protein Kinases/metabolism
- Bone Morphogenetic Proteins/genetics
- Bone Morphogenetic Proteins/metabolism
- Coenzyme A Ligases/genetics
- Coenzyme A Ligases/metabolism
- Molecular Sequence Data
- Glycogen Synthase Kinase 3/genetics
- Glycogen Synthase Kinase 3/metabolism
- Smad Proteins, Receptor-Regulated/genetics
- Smad Proteins, Receptor-Regulated/metabolism
- Fatty Acids, Unsaturated/metabolism*
- Embryo, Nonmammalian/cytology
- Embryo, Nonmammalian/metabolism*
- Amino Acid Sequence
- Zebrafish/embryology
- Zebrafish/genetics
- Zebrafish/metabolism*
- Blotting, Western
- Sequence Homology, Amino Acid
- Body Patterning/physiology*
- Gene Expression Regulation, Developmental*
- PubMed
- 24332754 Full text @ Dev. Cell
Long-chain polyunsaturated fatty acids (LC-PUFA) and their metabolites are critical players in cell biology and embryonic development. Here we show that long-chain acyl-CoA synthetase 4a (Acsl4a), an LC-PUFA activating enzyme, is essential for proper patterning of the zebrafish dorsoventral axis. Loss of Acsl4a results in dorsalized embryos due to attenuated bone morphogenetic protein (Bmp) signaling. We demonstrate that Acsl4a modulates the activity of Smad transcription factors, the downstream mediators of Bmp signaling. Acsl4a promotes the inhibition of p38 mitogen-activated protein kinase and the Akt-mediated inhibition of glycogen synthase kinase 3, critical inhibitors of Smad activity. Consequently, introduction of a constitutively active Akt can rescue the dorsalized phenotype of Acsl4a-deficient embryos. Our results reveal a critical role for Acsl4a in modulating Bmp-Smad activity and provide a potential avenue for LC-PUFAs to influence a variety of developmental processes.