Ju Bong-Gun, Solum Derek, Song Eun Joo, Lee Kong-Joo, Rose David W, Glass Christopher K, Rosenfeld Michael G
Howard Hughes Medical Institute, University of California, San Diego, Department and School of Medicine, La Jolla, CA 92093, USA.
Cell. 2004 Dec 17;119(6):815-29. doi: 10.1016/j.cell.2004.11.017.
Switching specific patterns of gene repression and activation in response to precise temporal/spatial signals is critical for normal development. Here we report a pathway in which induction of CaMKIIdelta triggers an unexpected switch in the function of the HES1 transcription factor from a TLE-dependent repressor to an activator required for neuronal differentiation. These events are based on activation of the poly(ADP-ribose) polymerase1 (PARP-1) sensor component of the groucho/TLE-corepressor complex mediating dismissal of the corepressor complex from HES1-regulated promoters. In parallel, CaMKIIdelta mediates a required phosphorylation of HES1 to permit neurogenic gene activation, revealing the ability of a specific signaling pathway to modulate both the derepression and the subsequent coactivator recruitment events required for transcriptional activation of a neurogenic program. The identification of PARP-1 as a regulated promoter-specific exchange factor required for activation of specific neurogenic gene programs is likely to be prototypic of similar molecular mechanisms.
响应精确的时空信号,切换特定的基因抑制和激活模式对于正常发育至关重要。在此,我们报告了一条信号通路,其中CaMKIIdelta的诱导引发了HES1转录因子功能的意外转变,即从依赖TLE的阻遏物转变为神经元分化所需的激活剂。这些事件基于groucho/TLE共抑制复合物的聚(ADP - 核糖)聚合酶1(PARP - 1)传感成分的激活,该成分介导共抑制复合物从HES1调控的启动子上解离。同时,CaMKIIdelta介导HES1的必要磷酸化以允许神经源性基因激活,揭示了特定信号通路调节神经源性程序转录激活所需的去抑制和随后的共激活因子募集事件的能力。PARP - 1作为激活特定神经源性基因程序所需的受调控的启动子特异性交换因子的鉴定,可能是类似分子机制的原型。