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Research Article Free access | 10.1172/JCI119862
Division of Cardiovascular Research, Research Institute, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada.
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Division of Cardiovascular Research, Research Institute, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada.
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Division of Cardiovascular Research, Research Institute, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada.
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Division of Cardiovascular Research, Research Institute, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada.
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Division of Cardiovascular Research, Research Institute, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, M5G 1X8, Canada.
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Published December 15, 1997 - More info
Intimal cushions form in the fetal ductus arteriosus by fibronectin-dependent smooth muscle cell migration which is associated with greater efficiency of fibronectin mRNA translation. We investigated whether the AU-rich element (ARE), UUAUUUAU, in the 3'-untranslated region (3'UTR) of fibronectin mRNA is involved in this mechanism by transfecting smooth muscle cells with plasmids containing the chloramphenicol acetyltransferase coding region with its 3'UTR replaced by fibronectin 3'UTR bearing intact or mutated ARE. More efficient translation of fusion mRNA with intact versus mutated ARE was observed. This effect was amplified in ductus (10.9-fold) compared with nonmigratory, lower fibronectin-producing aorta cells (6.5-fold). Ductus cells transfected with wild-type but not ARE-mutated plasmid reverted to the stellate phenotype of aorta cells associated with reduced fibronectin production. This suggested that plasmid ARE sequesters RNA-binding factors, thereby reducing endogenous fibronectin mRNA translation. We next purified a 15-kD fibronectin ARE-dependent RNA-binding protein and identified it as microtubule-associated protein 1 light chain 3 (LC3). LC3 is present in greater amounts in ductus compared with aorta cells, and overexpression of LC3 in aortic cells by transfection enhances fibronectin mRNA translation to levels observed in ductus cells.