Franklin J Matthew, Dubocanin Danilo, Chittenden Cy, Barillas Ashlie, Lee Rosa Jooyoung, Ghosh Rajarshi P, Gerton Jennifer L, Guan Kun-Liang, Altemose Nicolas
Department of Genetics, Stanford University, Palo Alto, CA 94304, USA.
Department of Molecular & Cell Biology, University of California, Berkeley, CA 94720, USA.
bioRxiv. 2025 Mar 21:2024.10.22.616524. doi: 10.1101/2024.10.22.616524.
Eukaryotic genomes frequently contain large arrays of tandem repeats, called satellite DNA. While some satellite DNAs participate in centromere function, others do not. For example, Human Satellite 3 (HSat3) forms the largest satellite DNA arrays in the human genome, but these multi-megabase regions were almost fully excluded from genome assemblies until recently, and their potential functions remain understudied and largely unknown. To address this, we performed a systematic screen for HSat3 binding proteins. Our work revealed that HSat3 contains millions of copies of transcription factor (TF) motifs bound by over a dozen TFs from various signaling pathways, including the growth-regulating transcription effector family TEAD1-4 from the Hippo pathway. Imaging experiments show that TEAD recruits the co-activator YAP to HSat3 regions in a cell-state specific manner. Using synthetic reporter assays, targeted repression of HSat3, inducible degradation of YAP, and super-resolution microscopy, we show that HSat3 arrays can localize YAP/TEAD inside the nucleolus, enhancing RNA Polymerase I activity. Beyond discovering a direct relationship between the Hippo pathway and ribosomal DNA regulation, this work demonstrates that satellite DNA can encode multiple transcription factor binding motifs, defining an important functional role for these enormous genomic elements.
真核生物基因组经常包含大量串联重复序列,称为卫星DNA。虽然一些卫星DNA参与着丝粒功能,但其他的则不然。例如,人类卫星3(HSat3)在人类基因组中形成了最大的卫星DNA阵列,但直到最近,这些数百万碱基对的区域几乎完全被排除在基因组组装之外,其潜在功能仍未得到充分研究且大多未知。为了解决这个问题,我们对HSat3结合蛋白进行了系统筛选。我们的研究表明,HSat3包含数百万个转录因子(TF)基序拷贝,这些基序被来自各种信号通路的十几种TF所结合,包括来自Hippo通路的生长调节转录效应因子家族TEAD1-4。成像实验表明,TEAD以细胞状态特异性方式将共激活因子YAP招募到HSat3区域。使用合成报告基因检测、靶向抑制HSat3、诱导YAP降解和超分辨率显微镜技术,我们表明HSat3阵列可以将YAP/TEAD定位在核仁内,增强RNA聚合酶I的活性。除了发现Hippo通路与核糖体DNA调控之间的直接关系外,这项工作还表明卫星DNA可以编码多个转录因子结合基序,为这些巨大的基因组元件定义了重要的功能作用。