Differentiation and Transcription Laboratory, Peter MacCallum Cancer Centre and the Pathology Department, The University of Melbourne, Melbourne, Victoria, Australia.
PLoS One. 2011;6(12):e28394. doi: 10.1371/journal.pone.0028394. Epub 2011 Dec 2.
Mixl1 is a homeodomain transcription factor required for mesoderm and endoderm patterning during mammalian embryogenesis. Despite its crucial function in development, co-factors that modulate the activity of Mixl1 remain poorly defined. Here we report that Mixl1 interacts physically and functionally with the T-box protein Brachyury and related members of the T-box family of transcription factors. Transcriptional and protein analyses demonstrated overlapping expression of Mixl1 and Brachyury during embryonic stem cell differentiation. In vitro protein interaction studies showed that the Mixl1 with Brachyury associated via their DNA-binding domains and gel shift assays revealed that the Brachyury T-box domain bound to Mixl1-DNA complexes. Furthermore, luciferase reporter experiments indicated that association of Mixl1 with Brachyury and related T-box factors inhibited the transactivating potential of Mixl1 on the Gsc and Pdgfrα promoters. Our results indicate that the activity of Mixl1 can be modulated by protein-protein interactions and that T-box factors can function as negative regulators of Mixl1 activity.
Mixl1 是一种同源结构域转录因子,在哺乳动物胚胎发生过程中对于中胚层和内胚层的形成具有重要作用。尽管 Mixl1 在发育过程中具有关键作用,但其调节活性的共因子仍未得到很好的定义。在这里,我们报告 Mixl1 与 T 盒蛋白 Brachyury 和相关 T 盒家族转录因子在物理和功能上相互作用。转录和蛋白分析表明,Mixl1 和 Brachyury 在胚胎干细胞分化过程中具有重叠的表达。体外蛋白相互作用研究表明,Mixl1 与 Brachyury 通过其 DNA 结合域相互作用,凝胶迁移分析显示 Brachyury T 盒结构域与 Mixl1-DNA 复合物结合。此外,荧光素酶报告基因实验表明,Mixl1 与 Brachyury 和相关 T 盒因子的结合抑制了 Mixl1 在 Gsc 和 Pdgfrα 启动子上的转录激活潜力。我们的结果表明,Mixl1 的活性可以通过蛋白-蛋白相互作用进行调节,并且 T 盒因子可以作为 Mixl1 活性的负调节剂。