| Literature DB >> 20533406 |
Jingxia Xu1, Luke T Krebs, Thomas Gridley.
Abstract
The Notch signaling pathway is an evolutionarily-conserved intercellular signaling mechanism, and mutations in its components disrupt embryonic development in many organisms and cause inherited diseases in humans. The Jagged2 (Jag2) gene, which encodes a ligand for Notch pathway receptors, is required for craniofacial, limb, and T cell development. Mice homozygous for a Jag2 null allele die at birth from cleft palate, precluding study of Jag2 function in postnatal and adult mice. We have generated a Jag2 conditional null allele by flanking the first two exons of the Jag2 gene with loxP sites. Cre-mediated deletion of the Jag2(flox) allele generates the Jag2(del2) allele, which behaves genetically as a Jag2 null allele. This Jag2 conditional null allele will enable investigation of Jag2 function in a variety of tissue-specific contexts. 2010 Wiley-Liss, Inc.Entities:
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Year: 2010 PMID: 20533406 PMCID: PMC3114645 DOI: 10.1002/dvg.20626
Source DB: PubMed Journal: Genesis ISSN: 1526-954X Impact factor: 2.487