Department of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Biochem Biophys Res Commun. 2011 Sep 30;413(3):426-31. doi: 10.1016/j.bbrc.2011.08.108. Epub 2011 Aug 27.
Numb serves as a key regulator of Notch and Sonic Hedgehog signaling and also modulates p53 protein levels. Numblike is a highly conserved homolog to mammalian Numb, but considerably less is known about its function. To address the role of Numblike, we have generated a mouse embryonic stem (ES) cell line, Nbl(TetOn), in which expression of Numblike can be induced and analyzed the effect of activation of Numblike. Induction of Numblike, similar to Numb, reduced the amount of Notch receptor, whereas Numblike differed from Numb with regard to p53 and Shh signaling. In contrast to Numb, Numblike did not elevate the level of p53 protein and Numblike potentiated, rather than reduced, the immediate downstream response of Shh signaling. In keeping with a role for Numblike in potentiating Shh signaling, Shh and Numblike synergistically increased the proportion of ES cells expressing pluripotency markers. In conclusion, the data demonstrate that Numb and Numblike have evolved to acquire at least partially distinct functions.
Num 作为 Notch 和 Sonic Hedgehog 信号的关键调节因子,还调节 p53 蛋白水平。Numblike 是哺乳动物 Num 的高度保守同源物,但对其功能的了解要少得多。为了研究 Numblike 的作用,我们生成了一种小鼠胚胎干细胞 (ES) 细胞系 Nbl(TetOn),其中可以诱导 Numblike 的表达并分析其激活的效果。与 Numb 相似,Numblike 的诱导降低了 Notch 受体的数量,而 Numblike 在 p53 和 Shh 信号方面与 Numb 不同。与 Numb 不同,Numblike 不会升高 p53 蛋白的水平,并且 Numblike 增强而不是降低了 Shh 信号的即时下游反应。与 Numblike 在增强 Shh 信号中的作用一致,Shh 和 Numblike 协同增加了表达多能性标记的 ES 细胞的比例。总之,这些数据表明 Numb 和 Numblike 已经进化到至少具有部分不同的功能。