pubmed-article:10495268 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0043342 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0599851 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0037083 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0430054 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C1521991 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0086860 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C1520113 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0439851 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C1710082 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C1456348 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C1705053 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C1552596 | lld:lifeskim |
pubmed-article:10495268 | lifeskim:mentions | umls-concept:C1947931 | lld:lifeskim |
pubmed-article:10495268 | pubmed:issue | 1-2 | lld:pubmed |
pubmed-article:10495268 | pubmed:dateCreated | 2000-3-16 | lld:pubmed |
pubmed-article:10495268 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:abstractText | The co-activation of Wnt signaling and concomitant inhibition of BMP signaling has previously been implicated in vertebrate neural patterning, as evidenced by the combinatorial induction of engrailed-2 and krox-20 in Xenopus. However, screens have not previously been conducted to identify additional potential target genes. Using a PCR-based screening method we determined that XA-1, xCRISP, UVS.2, two UVS.2-related genes, and xONR1 are induced in response to Xwnt-3a and a BMP-antagonist, noggin. Two additional genes, connexin 30 and retinoic acid receptor gamma were induced by Xwnt-3a alone. To determine whether any of the induced genes are direct targets of Wnt signaling, we focussed on engrailed-2. In the present study we show that the Xenopus engrailed-2 promoter contains three consensus binding sites for LEF/TCF, which are HMG box transcription factors which bind to beta-catenin in response to activation of the Wnt- 1 signaling pathway. An engrailed-2 promoter luciferase reporter construct containing these LEF/TCF sites is induced in embryo explant assays by the combination of Xwnt-3a or beta-catenin and noggin. These LEF/TCF sites are required for expression of engrailed-2, as a dominant negative Xtcf-3 blocks expression of endogenous engrailed-2 as well as expression of the reporter construct. Moreover, mutation of these three LEF/TCF sites abrogates expression of the reporter construct in response to noggin and Xwnt-3a or beta-catenin. We conclude that the engrailed-2 gene is a direct target of the Wnt signaling pathway, and that Wnt signaling works with BMP antagonists to regulate gene expression during patterning of the developing nervous system of Xenopus. | lld:pubmed |
pubmed-article:10495268 | pubmed:language | eng | lld:pubmed |
pubmed-article:10495268 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10495268 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10495268 | pubmed:month | Sep | lld:pubmed |
pubmed-article:10495268 | pubmed:issn | 0925-4773 | lld:pubmed |
pubmed-article:10495268 | pubmed:author | pubmed-author:BatesRR | lld:pubmed |
pubmed-article:10495268 | pubmed:author | pubmed-author:MoonR TRT | lld:pubmed |
pubmed-article:10495268 | pubmed:author | pubmed-author:McGrewL LLL | lld:pubmed |
pubmed-article:10495268 | pubmed:author | pubmed-author:TakemaruKK | lld:pubmed |
pubmed-article:10495268 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10495268 | pubmed:volume | 87 | lld:pubmed |
pubmed-article:10495268 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10495268 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10495268 | pubmed:pagination | 21-32 | lld:pubmed |
pubmed-article:10495268 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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pubmed-article:10495268 | pubmed:year | 1999 | lld:pubmed |
pubmed-article:10495268 | pubmed:articleTitle | Direct regulation of the Xenopus engrailed-2 promoter by the Wnt signaling pathway, and a molecular screen for Wnt-responsive genes, confirm a role for Wnt signaling during neural patterning in Xenopus. | lld:pubmed |
pubmed-article:10495268 | pubmed:affiliation | Howard Hughes Medical Institute, Department of Pharmacology and Center for Developmental Biology, University of Washington School of Medicine, Seattle, WA 98195, USA. | lld:pubmed |
pubmed-article:10495268 | pubmed:publicationType | Journal Article | lld:pubmed |