Lee Hansol, Quinn John C, Prasanth Kannanganattu V, Swiss Victoria A, Economides Kyriakos D, Camacho Marie M, Spector David L, Abate-Shen Cory
Center for Advanced Biotechnology and Medicine, Piscataway, New Jersey 08854, USA.
Genes Dev. 2006 Apr 1;20(7):784-94. doi: 10.1101/gad.1392006.
The mechanisms by which homeoproteins bind selectively to target genes in vivo have long remained unresolved. Here we report that PIAS1 confers DNA-binding specificity on the Msx1 homeoprotein by regulating its subnuclear localization and proximity to target genes. We demonstrate that the interaction of Msx1 with PIAS1, but not its sumoylation, is required for Msx1 to function as an inhibitor of myoblast differentiation through repression of myogenic regulatory genes, such as MyoD. We find that PIAS1 enables Msx1 to bind selectively to a key regulatory element in MyoD, the CER, in myoblast cells and to distinguish the CER from other nonregulatory TAAT-containing sequences. We show that PIAS1 is required for the appropriate localization and retention of Msx1 at the nuclear periphery in myoblast cells. Furthermore, we demonstrate that myogenic regulatory genes that are repressed by Msx1, namely MyoD and Myf5, are located at the nuclear periphery in myoblast cells. We propose that a key regulatory event for DNA-binding specificity by homeoproteins in vivo is their appropriate targeting to subnuclear compartments where their target genes are located, which can be achieved by cofactors such as PIAS1.
同源结构域蛋白在体内选择性结合靶基因的机制长期以来一直未得到解决。在此我们报告,PIAS1通过调节Msx1同源结构域蛋白的核内亚定位及其与靶基因的接近程度,赋予其DNA结合特异性。我们证明,Msx1与PIAS1的相互作用而非其SUMO化,是Msx1通过抑制成肌调节基因(如MyoD)发挥成肌细胞分化抑制剂功能所必需的。我们发现,PIAS1使Msx1能够在成肌细胞中选择性结合MyoD中的关键调节元件CER,并将CER与其他含TAAT的非调节序列区分开来。我们表明,PIAS1是Msx1在成肌细胞中在核周边正确定位和滞留所必需的。此外,我们证明被Msx1抑制的成肌调节基因,即MyoD和Myf5,位于成肌细胞的核周边。我们提出,同源结构域蛋白在体内实现DNA结合特异性的一个关键调节事件是它们正确靶向其靶基因所在的核亚区室,这可通过PIAS1等辅助因子来实现。