Kroeger Benjamin, Manning Samuel A, Mohan Varshini, Lou Jieqiong, Sun Guizhi, Lamont Sara, McCann Alex J, Francois Mathias, Polo Jose M, Hinde Elizabeth, Harvey Kieran F
Department of Anatomy and Developmental Biology, Monash University, Clayton, VIC 3800, Australia.
Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, VIC 3000, Australia.
Sci Adv. 2025 Jul 25;11(30):eadw4974. doi: 10.1126/sciadv.adw4974.
Over the past two decades, genetic and proteomic screens have identified the Hippo pathway as a complex signaling network that controls tissue growth and human cancer. Despite these advances, our understanding of how Hippo signaling regulates transcription is less clear. To address this, we used live microscopy to study the nuclear behavior of the major Hippo pathway transcription effectors, YAP and TEADs. We reveal that TEADs are a major determinant of YAP DNA binding and nuclear mobility, while YAP minorly influences TEADs. YAP and TEAD1 associate with DNA for longer periods in cells with intrinsically low Hippo pathway activity and upon acute Hippo pathway perturbation. TEAD1 binds the genome on a broad range of timescales, and this is extended substantially in nuclear condensates. Last, a cancer-associated YAP fusion protein exhibits substantially different biophysical behavior than either YAP or TEAD1. Thus, we reveal that Hippo signaling regulates transcription, in part, by influencing the DNA binding times of YAP and TEADs.
在过去二十年中,基因和蛋白质组筛选已将Hippo信号通路确定为一个控制组织生长和人类癌症的复杂信号网络。尽管取得了这些进展,但我们对Hippo信号如何调节转录的理解仍不太清楚。为了解决这个问题,我们使用活细胞显微镜技术研究了主要的Hippo信号通路转录效应因子YAP和TEADs的核行为。我们发现TEADs是YAP与DNA结合及核内移动性的主要决定因素,而YAP对TEADs的影响较小。在Hippo信号通路内在活性低的细胞以及急性Hippo信号通路扰动时,YAP和TEAD1与DNA结合的时间更长。TEAD1在广泛的时间尺度上与基因组结合,而在核凝聚物中这种结合时间大幅延长。最后,一种与癌症相关的YAP融合蛋白表现出与YAP或TEAD1截然不同的生物物理行为。因此,我们发现Hippo信号通路部分地通过影响YAP和TEADs与DNA的结合时间来调节转录。