The Center for Stem Cell Biology and Developmental Biology program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Curr Opin Genet Dev. 2024 Apr;85:102164. doi: 10.1016/j.gde.2024.102164. Epub 2024 Feb 27.
During brain development, the sequence of developmental steps and the underlying transcriptional regulatory logic are largely conserved across species. However, the temporal unfolding of developmental programs varies dramatically across species and within a given species varies across brain regions and cell identities. The maturation of neurons in the human cerebral cortex is particularly slow and lasts for many years compared with only a few weeks for the corresponding mouse neurons. The mechanisms setting the 'schedule' of neuronal maturation remain unclear but appear to be linked to a cell-intrinsic 'clock'. Here, we discuss recent findings that highlight a role for epigenetic factors in the timing of neuronal maturation. Manipulations of those factors in stem cell-based models can override the intrinsic pace of neuronal maturation, including its protracted nature in human cortical neurons. We then contextualize the epigenetic regulation of maturation programs with findings from other model systems and propose potential interactions between epigenetic pathways and other drivers of developmental rates.
在大脑发育过程中,发育步骤的顺序和潜在的转录调控逻辑在很大程度上是在物种间保守的。然而,发育程序的时间展开在物种间差异很大,在给定的物种内,也在脑区和细胞身份间存在差异。与对应于小鼠神经元的仅数周相比,人类大脑皮层中的神经元成熟特别缓慢,并且持续多年。设定神经元成熟“时间表”的机制仍不清楚,但似乎与细胞内在的“时钟”有关。在这里,我们讨论了最近的发现,这些发现强调了表观遗传因素在神经元成熟时间中的作用。在基于干细胞的模型中对这些因素的操作可以覆盖神经元成熟的内在节奏,包括人类皮质神经元成熟的延长性质。然后,我们将成熟程序的表观遗传调控与其他模型系统的发现联系起来,并提出表观遗传途径与发育速度的其他驱动因素之间可能存在的相互作用。