
doi: 10.1038/nn792
pmid: 11788835
Neurofibromatosis type 1 (NF1) is a dominant genetic disorder characterized by multiple benign and malignant nervous system tumors, and by learning defects in 45% of children with NF1 mutations. Studies of neurofibromin, the protein encoded by NF1, have focused on its functions in tumorigenesis and regulation of Ras activity; however, Drosophila NF1 regulates both Ras and cyclic AMP (cAMP) pathways. Expression of a human NF1 transgene rescued cAMP-related phenotypes in NF1 mutant flies (small body size and G protein-stimulated adenylyl cyclase (AC) activity defects), and neuropeptide- and G protein-stimulated AC activity were lower in Nf1-/- as compared to Nf1+/- mouse brains, demonstrating that neurofibromin regulates AC activity in both mammals and flies.
Mice, Knockout, Neurofibromin 1, Mice, GTP-Binding Proteins, Genes, Neurofibromatosis 1, Mutation, Animals, Humans, Drosophila, Transgenes, Adenylyl Cyclases
Mice, Knockout, Neurofibromin 1, Mice, GTP-Binding Proteins, Genes, Neurofibromatosis 1, Mutation, Animals, Humans, Drosophila, Transgenes, Adenylyl Cyclases
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