Max-Planck-Institute of Immunobiology, Freiburg, Germany.
Genes Dev. 2010 Mar 15;24(6):590-601. doi: 10.1101/gad.563210.
Timely acquisition of cell fates and the elaborate control of growth in numerous organs depend on Notch signaling. Upon ligand binding, the core transcription factor RBP-J activates transcription of Notch target genes. In the absence of signaling, RBP-J switches off target gene expression, assuring the tight spatiotemporal control of the response by a mechanism incompletely understood. Here we show that the histone demethylase KDM5A is an integral, conserved component of Notch/RBP-J gene silencing. Methylation of histone H3 Lys 4 is dynamically erased and re-established at RBP-J sites upon inhibition and reactivation of Notch signaling. KDM5A interacts physically with RBP-J; this interaction is conserved in Drosophila and is crucial for Notch-induced growth and tumorigenesis responses.
细胞命运的及时获得和众多器官中生长的精细控制依赖于 Notch 信号。配体结合后,核心转录因子 RBP-J 激活 Notch 靶基因的转录。在没有信号的情况下,RBP-J 关闭靶基因的表达,通过一种不完全清楚的机制确保了反应的严格时空控制。在这里,我们表明组蛋白去甲基化酶 KDM5A 是 Notch/RBP-J 基因沉默的一个完整的、保守的组成部分。H3K4 的甲基化在 Notch 信号抑制和再激活时在 RBP-J 位点动态地被清除和重新建立。KDM5A 与 RBP-J 发生物理相互作用;这种相互作用在果蝇中是保守的,对 Notch 诱导的生长和肿瘤发生反应至关重要。