Nishimoto Satoko, Kusakabe Morioh, Nishida Eisuke
Department of Cell and Developmental Biology, Graduate School of Biostudies, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.
EMBO Rep. 2005 Nov;6(11):1064-9. doi: 10.1038/sj.embor.7400515. Epub 2005 Sep 23.
Although previous studies have identified several key transcription factors in the generation process of the vertebrate nervous system, the intracellular signalling pathways that function in this process have remained unclear. Here we identify the evolutionarily conserved mitogen-activated protein kinase kinase 5 (MEK5)-extracellular signal-regulated kinase 5 (ERK5) pathway as an essential regulator in neural differentiation. Knockdown of Xenopus ERK5 or Xenopus MEK5 with antisense morpholino oligonucleotides results in the reduced head structure and inhibition of neural differentiation. Moreover, forced activation of the MEK5-ERK5 module on its own induces neural differentiation. In addition, we show that the MEK5-ERK5 pathway is necessary for the neuralizing activity of SoxD, a regulator of neural differentiation, and is sufficient for the expression of Xngnr1, a proneural gene. These results show that the MEK5-ERK5 pathway has an essential role in the regulation of neural differentiation downstream of SoxD and upstream of Xngnr1.
尽管先前的研究已经在脊椎动物神经系统的生成过程中鉴定出了几种关键转录因子,但在此过程中起作用的细胞内信号通路仍不清楚。在这里,我们确定进化上保守的丝裂原活化蛋白激酶激酶5(MEK5)-细胞外信号调节激酶5(ERK5)通路是神经分化中的一个重要调节因子。用反义吗啉代寡核苷酸敲低非洲爪蟾ERK5或非洲爪蟾MEK5会导致头部结构减少并抑制神经分化。此外,单独强制激活MEK5-ERK5模块会诱导神经分化。此外,我们表明MEK5-ERK5通路对于神经分化调节因子SoxD的神经化活性是必需的,并且足以诱导神经前体基因Xngnr1的表达。这些结果表明,MEK5-ERK5通路在SoxD下游和Xngnr1上游的神经分化调节中起重要作用。