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Hes6对皮质星形胶质细胞分化的抑制作用需要对二聚化和磷酸化至关重要的氨基末端和羧基末端基序。

Inhibition of cortical astrocyte differentiation by Hes6 requires amino- and carboxy-terminal motifs important for dimerization and phosphorylation.

作者信息

Belanger-Jasmin Stephanie, Llamosas Estelle, Tang Yeman, Joachim Kerline, Osiceanu Ana-Maria, Jhas Sumit, Stifani Stefano

机构信息

Center for Neuronal Survival, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.

出版信息

J Neurochem. 2007 Dec;103(5):2022-34. doi: 10.1111/j.1471-4159.2007.04902.x. Epub 2007 Sep 14.

DOI:10.1111/j.1471-4159.2007.04902.x
PMID:17868320
Abstract

Hairy/Enhancer of split (Hes) 6 is a basic helix-loop-helix protein that interacts with the transcriptional co-repressor, Groucho, and antagonizes the neural functions of the Notch pathway. More specifically, mouse Hes6 regulates cerebral corticogenesis by promoting neurogenesis and suppressing astrocyte differentiation. The molecular mechanisms underlying the anti-astrogenic function of Hes6 are poorly defined. Here we describe studies aimed at testing whether Hes6 inhibits astrocyte differentiation by antagonizing the transcription repression activity of Notch-activated Hes family members like Hes1. It is reported that Hes6 preferentially forms homodimers. Heterodimerization with Hes1 is antagonized in part by a conserved N-terminal patch of negatively charged residues. Mutation of this motif enhances heterodimerization with Hes1 and increases Hes6 ability to antagonize Hes1-mediated transcriptional repression. However, this mutation does not increase, but instead decreases, the anti-astrogenic activity of Hes6. It is shown further that Hes6 harbors a second conserved sequence, a C-terminal SPXXSP motif. This sequence is phosphorylated by the mitogen activated protein kinase pathway and its mutation disrupts the anti-astrogenic activity of Hes6 without affecting its ability to suppress Hes1. Together, these observations suggest that Hes6 homodimers regulate astrocyte differentiation through mechanisms that depend on the phosphorylation of Hes6 C-terminal domain but are independent of its ability to suppress Hes1-mediated transcriptional repression.

摘要

毛状/分裂增强子(Hes)6是一种碱性螺旋-环-螺旋蛋白,它与转录共抑制因子Groucho相互作用,并拮抗Notch信号通路的神经功能。更具体地说,小鼠Hes6通过促进神经发生和抑制星形胶质细胞分化来调节大脑皮质的形成。Hes6抗星形胶质细胞生成功能的分子机制尚不清楚。在此,我们描述了旨在测试Hes6是否通过拮抗Notch激活的Hes家族成员(如Hes1)的转录抑制活性来抑制星形胶质细胞分化的研究。据报道,Hes6优先形成同二聚体。与Hes1的异二聚化部分被一个保守的带负电荷残基的N端区域所拮抗。该基序的突变增强了与Hes1的异二聚化,并增加了Hes6拮抗Hes1介导的转录抑制的能力。然而,这种突变并没有增加,反而降低了Hes6的抗星形胶质细胞生成活性。进一步研究表明,Hes6含有第二个保守序列,即C端的SPXXSP基序。该序列被丝裂原活化蛋白激酶途径磷酸化,其突变破坏了Hes6的抗星形胶质细胞生成活性,而不影响其抑制Hes1的能力。总之,这些观察结果表明,Hes6同二聚体通过依赖于Hes6 C端结构域磷酸化但独立于其抑制Hes1介导的转录抑制能力的机制来调节星形胶质细胞分化。

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