Cao Ying, Knöchel Sigrun, Oswald Franz, Donow Cornelia, Zhao Hui, Knöchel Walter
Abteilung Biochemie, Universität Ulm, Albert-Einstein-Allee 11, D-89081 Ulm, Germany.
Mech Dev. 2006 Jan;123(1):84-96. doi: 10.1016/j.mod.2005.09.003. Epub 2005 Nov 8.
The active form of the Xenopus X-box binding protein 1 (xXBP1) partially synergizes and partially antagonizes with BMP-4 signaling. xXBP1 overexpression inhibits mesoderm differentiation and formation of neural tissues. A functional knockdown promotes differentiation of lateral and dorsal mesoderm but not of ventral mesoderm and of neuroectoderm. We show that the active form of xXBP1 in gastrula and early neurula stage embryos is generated by removal of exon 4 and not by an endoribonuclease activity in the endoplasmic reticulum. The N-terminal region of xXBP1 which contains the basic leucine-zipper also contains a nuclear localization signal and both, the N-terminal as well as the C-terminal regions are required for xXBP1 function. The effects of xXBP1 are in part correlated to a regulatory loop between xXBP1 and BMP-4. xXBP1 and BMP-4 stimulate mutually the transcription of each other, but xXBP1 inhibits the BMP-4 target gene, Xvent-2. Both, in vitro and in vivo assays demonstrate that xXBP1 interacts with BMP-4 and Xvent-2B promoters. GST-pulldown assays reveal that xXBP1 can interact with c-Jun, the transcriptional co-activator p300 and with the BMP-4 responsive Smad1. On the other hand, xXBP1 also binds to the inhibitory Smads, Smad6 and Smad7, that can act as transcriptional co-repressors. Based on these data, we conclude that xXBP1 might function as an inhibitor of mesodermal and neural tissue formation by acting either as transcriptional activator or as repressor. This dual activity depends upon binding of co-factors being involved in the formation of distinct transcription complexes.
非洲爪蟾X盒结合蛋白1(xXBP1)的活性形式与骨形态发生蛋白-4(BMP-4)信号传导部分协同、部分拮抗。xXBP1过表达会抑制中胚层分化和神经组织形成。功能性敲低可促进外侧和背侧中胚层而非腹侧中胚层和神经外胚层的分化。我们发现,原肠胚和早期神经胚阶段胚胎中xXBP1的活性形式是通过外显子4的去除产生的,而非通过内质网中的核糖核酸内切酶活性产生。xXBP1含有碱性亮氨酸拉链的N端区域也包含一个核定位信号,xXBP1功能需要N端以及C端区域。xXBP1的作用部分与xXBP1和BMP-4之间的调控环相关。xXBP1和BMP-4相互刺激彼此的转录,但xXBP1抑制BMP-4靶基因Xvent-2。体外和体内实验均表明,xXBP1与BMP-4和Xvent-2B启动子相互作用。谷胱甘肽-S-转移酶(GST)沉降实验表明,xXBP1可与转录共激活因子c-Jun、p300以及BMP-4反应性Smad1相互作用。另一方面,xXBP1也与可作为转录共抑制因子的抑制性Smads,即Smad6和Smad7结合。基于这些数据,我们得出结论,xXBP1可能通过作为转录激活因子或阻遏因子发挥作用,从而作为中胚层和神经组织形成的抑制剂。这种双重活性取决于参与形成不同转录复合物的辅助因子的结合。