Goldstein R E, Jiménez G, Cook O, Gur D, Paroush Z
Department of Biochemistry, Hadassah Medical School, The Hebrew University, PO Box 12272, Jerusalem 91120, Israel.
Development. 1999 Sep;126(17):3747-55. doi: 10.1242/dev.126.17.3747.
The Groucho corepressor mediates negative transcriptional regulation in association with various DNA-binding proteins in diverse developmental contexts. We have previously implicated Groucho in Drosophila embryonic terminal patterning, showing that it is required to confine tailless and huckebein terminal gap gene expression to the pole regions of the embryo. Here we reveal an additional requirement for Groucho in this developmental process by establishing that Groucho mediates repressor activity of the Huckebein protein. Putative Huckebein target genes are derepressed in embryos lacking maternal groucho activity and biochemical experiments demonstrate that Huckebein physically interacts with Groucho. Using an in vivo repression assay, we identify a functional repressor domain in Huckebein that contains an FRPW tetrapeptide, similar to the WRPW Groucho-recruitment domain found in Hairy-related repressor proteins. Mutations in Huckebein's FRPW motif abolish Groucho binding and in vivo repression activity, indicating that binding of Groucho through the FRPW motif is required for the repressor function of Huckebein. Taken together with our earlier results, these findings show that Groucho-repression regulates sequential aspects of terminal patterning in Drosophila.
在不同的发育环境中,Groucho共抑制因子与各种DNA结合蛋白共同介导负转录调控。我们之前已表明Groucho参与果蝇胚胎末端模式形成,即它对于将无尾基因和驼背基因的末端间隙基因表达限制在胚胎的极区是必需的。在此,我们通过证实Groucho介导驼背蛋白的抑制活性,揭示了Groucho在这一发育过程中的额外需求。在缺乏母源Groucho活性的胚胎中,推定的驼背蛋白靶基因被去抑制,并且生化实验表明驼背蛋白与Groucho发生物理相互作用。利用体内抑制试验,我们在驼背蛋白中鉴定出一个功能性抑制结构域,该结构域含有一个FRPW四肽,类似于在毛相关抑制蛋白中发现的WRPW Groucho招募结构域。驼背蛋白的FRPW基序中的突变消除了Groucho结合及体内抑制活性,这表明通过FRPW基序结合Groucho是驼背蛋白发挥抑制功能所必需的。结合我们早期的结果,这些发现表明Groucho抑制作用调节果蝇末端模式形成的连续过程。