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Imaging analysis of mineralocorticoid receptor and importins in single living cells by using GFP color variants
Authors:Masayuki?Tanaka  Mayumi?Nishi  Masafumi?Morimoto  Tohru?Sugimoto  Mitsuhiro?KawataEmail author
Affiliation:(1) Department of Molecular, Cellular and Craniofacial Biology and the Birth Defects Center, University of Louisville, Louisville, KY 40292, USA;(2) Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA;(3) Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
Abstract:Signaling from the endothelin-A (Ednra) receptor is responsible for initiating multiple signaling pathways within neural crest cells (NCCs). Loss of this initiation is presumably the basis for the craniofacial defects observed in Ednra–/– embryos. However, it is not known whether continued Ednra signaling in NCC derivatives is required for subsequent development of the lower jaw. To address this question, mice containing loxP recombination sequences flanking a portion of the Ednra gene were bred with transgenic mice that express Cre recombinase under control of a Dlx5/6 enhancer element. We find that while Ednra gene inactivation within the mandibular arch of these Ednra conditional knockout embryos is detectable by embryonic day (E) 10.5, mandibular arch-specific gene expression is normal, as is overall mandible development. These results suggest that while Ednra receptor signaling is crucial for early NCC patterning, subsequent Ednra signaling is not essential for mandible bone development.This work was supported in part by grants from the National Institutes of Health and the American Heart Association to D.E.C.
Keywords:Craniofacial  Neural crest  loxP  Cre recombinase  Knockout mice  Transgenic mice
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