Department of Developmental Biology, Sloan-Kettering Institute, New York, NY, USA.
EMBO J. 2011 Jul 15;30(15):3120-33. doi: 10.1038/emboj.2011.218.
The Notch intracellular domain functions as a co-activator for the DNA-binding protein Suppressor of Hairless (Su(H)) to mediate myriad cell fate decisions. Notch pathway activity is balanced by transcriptional repression, mediated by Su(H) in concert with its Drosophila corepressor Hairless. We demonstrate that the Drosophila neural BEN-solo protein Insensitive (Insv) is a nuclear factor that inhibits Notch signalling during multiple peripheral nervous system cell fate decisions. Endogenous Insv was particularly critical when repressor activity of Su(H) was compromised. Reciprocally, ectopic Insv generated several Notch loss-of-function phenotypes, repressed most Notch targets in the E(spl)-C, and opposed Notch-mediated activation of an E(spl)m3-luc reporter. A direct role for Insv in transcriptional repression was indicated by binding of Insv to Su(H), and by strong chromatin immunoprecipitation of endogenous Insv to most E(spl)-C loci. Strikingly, ectopic Insv fully rescued sensory organ precursors in Hairless null clones, indicating that Insv can antagonize Notch independently of Hairless. These data shed first light on the in vivo function for a BEN-solo protein as an Su(H) corepressor in the Notch pathway regulating neural development.
Notch 细胞内结构域作为 DNA 结合蛋白 Suppressor of Hairless(Su(H))的共激活因子,介导众多细胞命运决定。Notch 途径的活性通过转录抑制来平衡,Su(H)与其果蝇核心抑制因子 Hairless 协同作用介导转录抑制。我们证明果蝇神经 BEN-solo 蛋白 Insensitive(Insv)是一种核因子,在多个周围神经系统细胞命运决定中抑制 Notch 信号。当 Su(H)的抑制活性受到损害时,内源性 Insv 尤为关键。相反,异位 Insv 产生了几种 Notch 功能丧失表型,抑制了 E(spl)-C 中的大多数 Notch 靶基因,并反对 Notch 介导的 E(spl)m3-luc 报告基因的激活。Insv 与 Su(H)结合,以及内源性 Insv 强烈的染色质免疫沉淀到大多数 E(spl)-C 基因座,表明 Insv 在转录抑制中具有直接作用。引人注目的是,异位 Insv 完全挽救了 Hairless 缺失克隆中的感觉器官前体细胞,表明 Insv 可以独立于 Hairless 拮抗 Notch。这些数据首次揭示了 BEN-solo 蛋白作为 Notch 通路中调节神经发育的 Su(H)核心抑制因子的体内功能。