Department of Biological Sciences, College of Natural Science, Inha University, 253 Yonghyun-dong, Nam-Gu, Incheon, Korea, 402-751.
Exp Cell Res. 2010 Feb 15;316(4):517-29. doi: 10.1016/j.yexcr.2009.12.003. Epub 2009 Dec 11.
Precisely controlled cellular differentiation is essential for the proper development of vertebrate embryo and deregulated differentiation is a major cause of many human congenital diseases as well as cancer. Msx1 is a member of the homeoprotein family implicated in these processes, which inhibits the differentiation of skeletal muscle and other cell types, presumably by regulating transcription of target genes through interaction with other cellular factors. We presently show that YB1/p32, a nuclear Y-box binding protein 1, interacts with Msx1 homeoprotein and functions as a regulator of C2C12 myoblast differentiation. We demonstrate that YB1/p32 functionally interacts with Msx1 through its N-terminal region and colocalizes with Msx1 at the nuclear periphery. Moreover, we find that YB1/p32 is competent for inhibition of C2C12 myoblast differentiation, which is correlated with its activity as a negative regulator of MyoD gene expression and binding to the MyoD core enhancer region (CER). Furthermore, YB1/p32 cooperates with Msx1 in transcriptional repression and knocking down the expression of endogenous YB1 attenuates the effects of Msx1. Taken together, our study has uncovered a new function of YB1/p32, a regulator of skeletal muscle differentiation.
精确控制细胞分化对于脊椎动物胚胎的正常发育至关重要,而分化失调是许多人类先天性疾病和癌症的主要原因。Msx1 是参与这些过程的同源蛋白家族的成员,它通过与其他细胞因子相互作用来调节靶基因的转录,从而抑制骨骼肌和其他细胞类型的分化。我们目前表明,YB1/p32,一种核 Y 框结合蛋白 1,与 Msx1 同源蛋白相互作用,并作为 C2C12 成肌细胞分化的调节剂发挥作用。我们证明 YB1/p32 通过其 N 端区域与 Msx1 进行功能相互作用,并与 Msx1 一起定位于核周。此外,我们发现 YB1/p32 能够抑制 C2C12 成肌细胞的分化,这与其作为 MyoD 基因表达的负调节剂和与 MyoD 核心增强子区域(CER)结合的活性相关。此外,YB1/p32 与 Msx1 合作进行转录抑制,敲低内源性 YB1 的表达会减弱 Msx1 的作用。总之,我们的研究揭示了 YB1/p32 的一个新功能,即调节骨骼肌分化。