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The homeodomain transcription factor NK-4 acts as either a transcriptional activator or repressor and interacts with the p300 coactivator and the Groucho corepressor.

DC Field Value Language
dc.contributor.authorChoi, CY-
dc.contributor.authorLee, YM-
dc.contributor.authorKim, YH-
dc.contributor.authorPark, T-
dc.contributor.authorJeon, BH-
dc.contributor.authorSchulz, RA-
dc.contributor.authorKim, Y-
dc.date.accessioned2011-09-16T05:12:17Z-
dc.date.available2011-09-16T05:12:17Z-
dc.date.issued1999-
dc.identifier.issn0021-9258-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/4193-
dc.description.abstractNK-4 (tinman) encodes an NK-2 class homeodomain transcription factor that is required for development of the Drosophila dorsal mesoderm, including heart. Genetic evidence suggests its important role in mesoderm subdivision, yet the properties of NK-4 as a transcriptional regulator and the mechanism of gene transcription by NK-4 are not completely understood. Here, we describe its properties as a transcription factor and its interaction with the p300 coactivator and the Groucho corepressor. We demonstrate that NK-4 can activate or repress target genes in cultured cells, depending on functional domains that are conserved between Drosophila melanogaster and Drosophila virilis NK-4 genes. Using GAL4-NK-4 fusion constructs, we have mapped a transcriptional activation domain (amino acids 1-110) and repression domains (amino acids 111-188 and the homeodomain) and found an inhibitory function for the homeodomain in transactivation by NK-4. Furthermore, we demonstrate that NK-4-dependent transactivation is augmented by the p300 coactivator and show that NK-4 physically interacts with p300 via the activation domain. In addition, cotransfection experiments indicate that the repressor activity of NK-4 is strongly enhanced by the Groucho corepressor. Using immunoprecipitation and in vitro pull-down assays, we show that NK-4 directly interacts with the Groucho corepressor, for which the homeodomain is required. Together, our results indicate that NK-4 can act as either a transcriptional activator or repressor and provide the first evidence of NK-4 interactions with the p300 coactivator and the Groucho corepressor.-
dc.language.isoen-
dc.subject.MESHAmino Acid Sequence-
dc.subject.MESHAnimals-
dc.subject.MESHBasic Helix-Loop-Helix Transcription Factors-
dc.subject.MESHBinding Sites-
dc.subject.MESHConserved Sequence-
dc.subject.MESHDNA-Binding Proteins-
dc.subject.MESHDrosophila-
dc.subject.MESHDrosophila Proteins-
dc.subject.MESHGene Expression Regulation-
dc.subject.MESHNuclear Proteins-
dc.subject.MESHPrecipitin Tests-
dc.subject.MESHProtein Binding-
dc.subject.MESHProtein Structure, Tertiary-
dc.subject.MESHRecombinant Fusion Proteins-
dc.subject.MESHRepressor Proteins-
dc.subject.MESHSequence Deletion-
dc.subject.MESHTrans-Activators-
dc.subject.MESHTranscription, Genetic-
dc.titleThe homeodomain transcription factor NK-4 acts as either a transcriptional activator or repressor and interacts with the p300 coactivator and the Groucho corepressor.-
dc.typeArticle-
dc.identifier.pmid10531357-
dc.identifier.urlhttp://www.jbc.org/cgi/pmidlookup?view=long&pmid=10531357-
dc.contributor.affiliatedAuthor이, 영미-
dc.type.localJournal Papers-
dc.citation.titleThe Journal of biological chemistry-
dc.citation.volume274-
dc.citation.number44-
dc.citation.date1999-
dc.citation.startPage31543-
dc.citation.endPage31552-
dc.identifier.bibliographicCitationThe Journal of biological chemistry, 274(44). : 31543-31552, 1999-
dc.identifier.eissn1083-351X-
dc.relation.journalidJ000219258-
Appears in Collections:
Journal Papers > Research Organization > Institute for Medical Sciences
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