Department of Medicine, Gastroenterology Division, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America; Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America; Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
PLoS One. 2015 Jan 30;10(1):e0117522. doi: 10.1371/journal.pone.0117522. eCollection 2015.
The Hippo pathway regulates cell proliferation and apoptosis through the Yes-associated protein (YAP) transcriptional activator. YAP has a well-described role in promoting cell proliferation and survival, but the precise mechanisms and transcriptional targets that underlie these properties are still unclear and likely context-dependent. We found, using siRNA-mediated knockdown, that YAP is required for proliferation in endothelial cells but not HeLa cells. Specifically, YAP is required for S-phase entry and its absence causes cells to accumulate in G1. Microarray analysis suggests that YAP mediates this effect by regulating the transcription of genes involved in the assembly and/or firing of replication origins and homologous recombination of DNA. These findings thus provide insight into the molecular mechanisms by which YAP regulates cell cycle progression.
Hippo 通路通过 Yes 相关蛋白(YAP)转录激活因子调节细胞增殖和凋亡。YAP 在促进细胞增殖和存活方面具有明确的作用,但这些特性背后的确切机制和转录靶标仍不清楚,且可能依赖于具体的上下文。我们通过 siRNA 介导的敲低发现,YAP 是内皮细胞而非 HeLa 细胞增殖所必需的。具体来说,YAP 是 S 期进入所必需的,其缺失会导致细胞在 G1 期积累。微阵列分析表明,YAP 通过调节参与复制起点组装和/或引发以及 DNA 同源重组的基因的转录来介导这种效应。这些发现因此为 YAP 调节细胞周期进程的分子机制提供了深入的了解。