The RGD motif in fibronectin is essential for development but dispensable for fibril assembly |
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Authors: | Takahashi Seiichiro Leiss Michael Moser Markus Ohashi Tomoo Kitao Tomoe Heckmann Dominik Pfeifer Alexander Kessler Horst Takagi Junichi Erickson Harold P Fässler Reinhard |
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Affiliation: | Max Planck Institute of Biochemistry, Department of Molecular Medicine, 82152 Martinsried, Germany. |
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Abstract: | Fibronectin (FN) is secreted as a disulfide-bonded FN dimer. Each subunit contains three types of repeating modules: FN-I, FN-II, and FN-III. The interactions of alpha5beta1 or alphav integrins with the RGD motif of FN-III repeat 10 (FN-III10) are considered an essential step in the assembly of FN fibrils. To test this hypothesis in vivo, we replaced the RGD motif with the inactive RGE in mice. FN-RGE homozygous embryos die at embryonic day 10 with shortened posterior trunk, absent tail bud-derived somites, and severe vascular defects resembling the phenotype of alpha5 integrin-deficient mice. Surprisingly, the absence of a functional RGD motif in FN did not compromise assembly of an FN matrix in mutant embryos or on mutant cells. Matrix assembly assays and solid-phase binding assays reveal that alphavbeta3 integrin assembles FN-RGE by binding an isoDGR motif in FN-I5, which is generated by the nonenzymatic rearrangement of asparagines (N) into an iso-aspartate (iso-D). Our findings demonstrate that FN contains a novel motif for integrin binding and fibril formation whose activity is controlled by amino acid modification. |
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