Identification and Cloning of the Human Homolog (JAG1) of the RatJagged1Gene from the Alagille Syndrome Critical Region at 20p12 |
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Authors: | Takaya Oda Abdel G. Elkahloun Paul S. Meltzer Settara C. Chandrasekharappa |
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Affiliation: | aLaboratory of Gene Transfer, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, 20892;bLaboratory of Cancer Genetics, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, 20892 |
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Abstract: | Notch proteins are a family of closely related transmembrane receptors proven to be instrumental in cell fate decisions. Recently, Notch ligands Delta and Jagged have been identified inDrosophilaand rat, respectively. We have isolated the human homolog of the ratJagged1gene,JAG1,from a CpG island in a YAC clone covering the Alagille syndrome critical region at chromosome 20p12 (tel–SNAP–D20S186–cen). Alagille syndrome is an autosomal dominant disorder characterized by neonatal jaundice, paucity of intrahepatic bile ducts, and abnormalities of the heart, skeleton, and eyes. The humanJagged1(JAG1), therefore, appears to be a strong candidate gene for this disease. Here we describe the identification, full-length cDNA cloning, expression patterns, and precise physical location of this gene within the Alagille syndrome critical region. |
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