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TEAD/TEF家族蛋白Scalloped介导Hippo生长调节通路的转录输出。

The TEAD/TEF family protein Scalloped mediates transcriptional output of the Hippo growth-regulatory pathway.

作者信息

Wu Shian, Liu Yi, Zheng Yonggang, Dong Jixin, Pan Duojia

机构信息

Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

Dev Cell. 2008 Mar;14(3):388-98. doi: 10.1016/j.devcel.2008.01.007. Epub 2008 Feb 7.

Abstract

The Hippo (Hpo) kinase cascade restricts tissue growth by inactivating the transcriptional coactivator Yorkie (Yki), which regulates the expression of target genes such as the cell death inhibitor diap1 by unknown mechanisms. Here we identify the TEAD/TEF family protein Scalloped (Sd) as a DNA-binding transcription factor that partners with Yki to mediate the transcriptional output of the Hpo growth-regulatory pathway. The diap1 (th) locus harbors a minimal Sd-binding Hpo Responsive Element (HRE) that mediates transcriptional regulation by the Hpo pathway. Sd binds directly to Yki, and a Yki missense mutation that abrogates Sd-Yki binding also inactivates Yki function in vivo. We further demonstrate that sd is required for yki-induced tissue overgrowth and target gene expression, and that sd activity is conserved in its mammalian homolog. Our results uncover a heretofore missing link in the Hpo signaling pathway and provide a glimpse of the molecular events on a Hpo-responsive enhancer element.

摘要

河马(Hpo)激酶级联通过使转录共激活因子约克蛋白(Yki)失活来限制组织生长,Yki通过未知机制调节诸如细胞死亡抑制剂diap1等靶基因的表达。在此,我们鉴定出TEAD/TEF家族蛋白扇贝蛋白(Sd)作为一种DNA结合转录因子,它与Yki协同作用,介导Hpo生长调节途径的转录输出。diap1(th)基因座含有一个最小的Sd结合Hpo反应元件(HRE),该元件介导Hpo途径的转录调控。Sd直接与Yki结合,一个消除Sd-Yki结合的Yki错义突变在体内也会使Yki功能失活。我们进一步证明,sd是yki诱导的组织过度生长和靶基因表达所必需的,并且sd活性在其哺乳动物同源物中是保守的。我们的结果揭示了Hpo信号通路中迄今缺失的一环,并提供了对Hpo反应增强子元件上分子事件的一瞥。

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