bfb,a Novel ENU-Induced blebs Mutant Resulting from a Missense Mutation in Fras1
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| Authors: | Kerry A. Miller Christopher T. Gordon Megan F. Welfare Georgina Caruana John F. Bertram John F. Bateman Peter G. Farlie |
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| Affiliation: | 1. Murdoch Children''s Research Institute, Royal Children''s Hospital, Parkville, Victoria, Australia.; 2. Departments of Paediatrics, Biochemistry and Molecular Biology, University of Melbourne, Parkville, Victoria, Australia.; 3. Department of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.; Pennington Biomedical Research Center/LSU, United States of America, |
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| Abstract: | Fras1 is an extracellular matrix associated protein with essential roles in adhesion of epithelia and mesenchyme during early embryonic development. The adhesive function of Fras1 is achieved through interaction with a group of related proteins, Frem 1–3, and a cytoplasmic adaptor protein Grip1. Mutation of each of these proteins results in characteristic epithelial blistering and have therefore become known as “blebs” proteins. Human Fraser syndrome presents with a similar phenotype and the blebs mice have been instrumental in identification of the genetic basis of Fraser syndrome. We have identified a new ENU-induced blebs allele resulting from a novel missense mutation in Fras1. The resulting mouse strain, blood filled blisters (bfb), presents with a classic blebs phenotype but does not exhibit embryonic lethality typical of other blebs mutants and in addition, we report novel palate and sternal defects. Analysis of the bfb phenotype confirms the presence of epithelial-mesenchymal adhesion defects but also supports the emerging role of blebs proteins in regulating signalling during organogenesis. The bfb strain provides new opportunities to investigate the role of Fras1 in development. |
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