| Literature DB >> 27389986 |
Thomas C B Wong1, Martha Rebbert, Chengdong Wang, Xiongfong Chen, Alison Heffer, Valeria E Zarelli, Igor B Dawid, Hui Zhao.
Abstract
Neural crest (NC) development is controlled precisely by a regulatory network with multiple signaling pathways and the involvement of many genes. The integration and coordination of these factors are still incompletely understood. Overexpression of Wnt3a and the BMP antagonist Chordin in animal cap cells from Xenopus blastulae induces a large number of NC specific genes. We previously suggested that Potassium Channel Tetramerization Domain containing 15 (Kctd15) regulates NC formation by affecting Wnt signaling and the activity of transcription factor AP-2. In order to advance understanding of the function of Kctd15 during NC development, we performed DNA microarray assays in explants injected with Wnt3a and Chordin, and identified genes that are affected by Kctd15 overexpression. Among the many genes identified, we chose Duf domain containing protein 1 (ddcp1), Platelet-Derived Growth Factor Receptor a (pdgfra), Complement factor properdin (cfp), Zinc Finger SWIM-Type Containing 5 (zswim5), and complement component 3 (C3) to examine their expression by whole mount in situ hybridization. Our work points to a possible role for Kctd15 in the regulation of NC formation and other steps in embryonic development.Entities:
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Year: 2016 PMID: 27389986 PMCID: PMC4987960 DOI: 10.1387/ijdb.160058id
Source DB: PubMed Journal: Int J Dev Biol ISSN: 0214-6282 Impact factor: 2.203