The Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.
Dev Cell. 2013 Aug 12;26(3):223-36. doi: 10.1016/j.devcel.2013.07.008.
The chromatin remodeler CHD5 is expressed in neural tissue and is frequently deleted in aggressive neuroblastoma. Very little is known about the function of CHD5 in the nervous system or its mechanism of action. Here we report that depletion of Chd5 in the developing neocortex blocks neuronal differentiation and leads to an accumulation of undifferentiated progenitors. CHD5 binds a large cohort of genes and is required for facilitating the activation of neuronal genes. It also binds a cohort of Polycomb targets and is required for the maintenance of H3K27me3 on these genes. Interestingly, the chromodomains of CHD5 directly bind H3K27me3 and are required for neuronal differentiation. In the absence of CHD5, a subgroup of Polycomb-repressed genes becomes aberrantly expressed. These findings provide insights into the regulatory role of CHD5 during neurogenesis and suggest how inactivation of this candidate tumor suppressor might contribute to neuroblastoma.
染色质重塑因子 CHD5 在神经组织中表达,并且在侵袭性神经母细胞瘤中经常缺失。关于 CHD5 在神经系统中的功能或其作用机制知之甚少。在这里,我们报告在发育中的新皮层中耗尽 Chd5 会阻止神经元分化,并导致未分化祖细胞的积累。CHD5 结合了一大批基因,并有助于促进神经元基因的激活。它还结合了一大批 Polycomb 靶基因,并需要维持这些基因上的 H3K27me3。有趣的是,CHD5 的 chromodomains 直接结合 H3K27me3,并对神经元分化至关重要。在没有 CHD5 的情况下,一小部分 Polycomb 抑制基因异常表达。这些发现为 CHD5 在神经发生过程中的调节作用提供了深入的了解,并表明这种候选肿瘤抑制因子的失活如何导致神经母细胞瘤的发生。