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B-cell translocation gene 2 (Btg2) regulates vertebral patterning by modulating bone morphogenetic protein/smad signaling.

DC Field Value Language
dc.contributor.authorPark, S-
dc.contributor.authorLee, YJ-
dc.contributor.authorLee, HJ-
dc.contributor.authorSeki, T-
dc.contributor.authorHong, KH-
dc.contributor.authorPark, J-
dc.contributor.authorBeppu, H-
dc.contributor.authorLim, IK-
dc.contributor.authorYoon, JW-
dc.contributor.authorLi, E-
dc.contributor.authorKim, SJ-
dc.contributor.authorOh, SP-
dc.date.accessioned2011-06-24T01:10:55Z-
dc.date.available2011-06-24T01:10:55Z-
dc.date.issued2004-
dc.identifier.issn0270-7306-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/3033-
dc.description.abstractBtg2 is a primary p53 transcriptional target gene which may function as a coactivator-corepressor and/or an adaptor molecule that modulates the activities of its interacting proteins. We have generated Btg2-null mice to elucidate the in vivo function of Btg2. Btg2-null mice are viable and fertile but exhibit posterior homeotic transformations of the axial vertebrae in a dose-dependent manner. Consistent with its role in vertebral patterning, Btg2 is expressed in the presomitic mesoderm, tail bud, and somites during somitogenesis. We further provide biochemical evidence that Btg2 interacts with bone morphogenetic protein (BMP)-activated Smads and enhances the transcriptional activity of BMP signaling. In view of the genetic evidence that reduced BMP signaling causes posteriorization of the vertebral pattern, we propose that the observed vertebral phenotype in Btg2-null mice is due to attenuated BMP signaling.-
dc.language.isoen-
dc.subject.MESHAlleles-
dc.subject.MESHAnimals-
dc.subject.MESHBlotting, Southern-
dc.subject.MESHBody Patterning-
dc.subject.MESHCell Line-
dc.subject.MESHDNA-Binding Proteins-
dc.subject.MESHDose-Response Relationship, Drug-
dc.subject.MESHEmbryo, Mammalian-
dc.subject.MESHExons-
dc.subject.MESHFemale-
dc.subject.MESHGene Expression Regulation, Developmental-
dc.subject.MESHGenes, Reporter-
dc.subject.MESHGenes, Tumor Suppressor-
dc.subject.MESHGenetic Vectors-
dc.subject.MESHHumans-
dc.subject.MESHImmediate-Early Proteins-
dc.subject.MESHImmunoblotting-
dc.subject.MESHImmunoprecipitation-
dc.subject.MESHIn Situ Hybridization-
dc.subject.MESHMale-
dc.subject.MESHMice-
dc.subject.MESHMice, Transgenic-
dc.subject.MESHModels, Genetic-
dc.subject.MESHMutation-
dc.subject.MESHRNA, Messenger-
dc.subject.MESHSignal Transduction-
dc.subject.MESHSmad Proteins-
dc.subject.MESHStem Cells-
dc.subject.MESHTrans-Activators-
dc.subject.MESHTranscription, Genetic-
dc.subject.MESHTransfection-
dc.subject.MESHTumor Suppressor Protein p53-
dc.subject.MESHTumor Suppressor Proteins-
dc.titleB-cell translocation gene 2 (Btg2) regulates vertebral patterning by modulating bone morphogenetic protein/smad signaling.-
dc.typeArticle-
dc.identifier.pmid15542835-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC529031/-
dc.contributor.affiliatedAuthor임, 인경-
dc.type.localJournal Papers-
dc.identifier.doi10.1128/MCB.24.23.10256-10262.2004-
dc.citation.titleMolecular and cellular biology-
dc.citation.volume24-
dc.citation.number23-
dc.citation.date2004-
dc.citation.startPage10256-
dc.citation.endPage10262-
dc.identifier.bibliographicCitationMolecular and cellular biology, 24(23). : 10256-10262, 2004-
dc.identifier.eissn1098-5549-
dc.relation.journalidJ002707306-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Biochemistry & Molecular Biology
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