Gratton Michel-Olivier, Torban Elena, Jasmin Stephanie Belanger, Theriault Francesca M, German Michael S, Stifani Stefano
Center for Neuronal Survival, Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada.
Mol Cell Biol. 2003 Oct;23(19):6922-35. doi: 10.1128/MCB.23.19.6922-6935.2003.
Hes1 is a mammalian basic helix-loop-helix transcriptional repressor that inhibits neuronal differentiation together with corepressors of the Groucho (Gro)/Transducin-like Enhancer of split (TLE) family. The interaction of Hes1 with Gro/TLE is mediated by a WRPW tetrapeptide present in all Hairy/Enhancer of split (Hes) family members. In contrast to Hes1, the related protein Hes6 promotes neuronal differentiation. Little is known about the molecular mechanisms that underlie the neurogenic activity of Hes6. It is shown here that Hes6 antagonizes Hes1 function by two mechanisms. Hes6 inhibits the interaction of Hes1 with its transcriptional corepressor Gro/TLE. Moreover, it promotes proteolytic degradation of Hes1. This effect is maximal when both Hes1 and Hes6 contain the WRPW motif and is reduced when Hes6 is mutated to eliminate a conserved site (Ser183) that can be phosphorylated by protein kinase CK2. Consistent with these findings, Hes6 inhibits Hes1-mediated transcriptional repression in cortical neural progenitor cells and promotes the differentiation of cortical neurons, a process that is normally inhibited by Hes1. Mutation of Ser183 impairs the neurogenic ability of Hes6. Taken together, these findings clarify the molecular events underlying the neurogenic function of Hes6 and suggest that this factor can antagonize Hes1 activity by multiple mechanisms.
Hes1是一种哺乳动物的碱性螺旋-环-螺旋转录抑制因子,它与Groucho(Gro)/分裂样转导素增强子(TLE)家族的共抑制因子一起抑制神经元分化。Hes1与Gro/TLE的相互作用由所有毛状/分裂增强子(Hes)家族成员中存在的WRPW四肽介导。与Hes1相反,相关蛋白Hes6促进神经元分化。关于Hes6神经源性活性的分子机制知之甚少。本文表明,Hes6通过两种机制拮抗Hes1的功能。Hes6抑制Hes1与其转录共抑制因子Gro/TLE的相互作用。此外,它促进Hes1的蛋白水解降解。当Hes1和Hes6都含有WRPW基序时,这种效应最大,而当Hes6发生突变以消除可被蛋白激酶CK2磷酸化的保守位点(Ser183)时,这种效应会减弱。与这些发现一致,Hes6抑制皮质神经祖细胞中Hes1介导的转录抑制,并促进皮质神经元的分化,而这一过程通常受到Hes1的抑制。Ser183的突变损害了Hes6的神经源性能力。综上所述,这些发现阐明了Hes6神经源性功能背后的分子事件,并表明该因子可通过多种机制拮抗Hes1的活性。