Laboratory of Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Nat Commun. 2020 Mar 19;11(1):1472. doi: 10.1038/s41467-020-15301-0.
The Hippo TEAD-transcriptional regulators YAP1 and TAZ are central for cell renewal and cancer growth; however, the specific downstream gene networks involved in their activity are not completely understood. Here we introduce TEADi, a genetically encoded inhibitor of the interaction of YAP1 and TAZ with TEAD, as a tool to characterize the transcriptional networks and biological effects regulated by TEAD transcription factors. Blockage of TEAD activity by TEADi in human keratinocytes and mouse skin leads to reduced proliferation and rapid activation of differentiation programs. Analysis of gene networks affected by TEADi and YAP1/TAZ knockdown identifies KLF4 as a central transcriptional node regulated by YAP1/TAZ-TEAD in keratinocyte differentiation. Moreover, we show that TEAD and KLF4 can regulate the activity of each other, indicating that these factors are part of a transcriptional regulatory loop. Our study establishes TEADi as a resource for studying YAP1/TAZ-TEAD dependent effects.
Hippo 通路的 TEAD 转录调控因子 YAP1 和 TAZ 是细胞更新和癌症生长的核心;然而,其活性涉及的特定下游基因网络尚不完全清楚。在这里,我们引入了 TEADi,这是一种基因编码的 YAP1 和 TAZ 与 TEAD 相互作用的抑制剂,作为一种工具来表征由 TEAD 转录因子调控的转录网络和生物学效应。在人角质形成细胞和小鼠皮肤中,TEADi 阻断 TEAD 活性会导致增殖减少和分化程序的快速激活。受 TEADi 和 YAP1/TAZ 敲低影响的基因网络分析确定 KLF4 是角质形成细胞分化中受 YAP1/TAZ-TEAD 调控的中央转录节点。此外,我们表明 TEAD 和 KLF4 可以相互调节彼此的活性,表明这些因子是转录调控环的一部分。我们的研究确立了 TEADi 作为研究 YAP1/TAZ-TEAD 依赖性效应的资源。