The homeodomain transcription factor NK-4 acts as either a transcriptional activator or repressor and interacts with the p300 coactivator and the Groucho corepressor
被引:53
作者:
Choi, CY
论文数: 0引用数: 0
h-index: 0
机构:NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
Choi, CY
Lee, YM
论文数: 0引用数: 0
h-index: 0
机构:NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
Lee, YM
Kim, YH
论文数: 0引用数: 0
h-index: 0
机构:NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
Kim, YH
Park, T
论文数: 0引用数: 0
h-index: 0
机构:NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
Park, T
Jeon, BH
论文数: 0引用数: 0
h-index: 0
机构:NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
Jeon, BH
Schulz, RA
论文数: 0引用数: 0
h-index: 0
机构:NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
Schulz, RA
Kim, Y
论文数: 0引用数: 0
h-index: 0
机构:NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
Kim, Y
机构:
[1] NHLBI, Mol Cardiol Lab, NIH, Bethesda, MD 20892 USA
[2] Konkuk Univ, Dept Mol Biol, Chungju, South Korea
[3] Univ Texas, MD Anderson Canc Ctr, Dept Biochem & Mol Biol, Houston, TX 77030 USA
NK-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 time 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.