Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Dev Cell. 2022 May 9;57(9):1193-1207.e7. doi: 10.1016/j.devcel.2022.04.008. Epub 2022 Apr 27.
Temporal patterning of neural progenitors is an evolutionarily conserved strategy for generating neuronal diversity. Type II neural stem cells in the Drosophila central brain produce transit-amplifying intermediate neural progenitors (INPs) that exhibit temporal patterning. However, the known temporal factors cannot account for the neuronal diversity in the adult brain. To search for missing factors, we developed NanoDam, which enables rapid genome-wide profiling of endogenously tagged proteins in vivo with a single genetic cross. Mapping the targets of known temporal transcription factors with NanoDam revealed that Homeobrain and Scarecrow (ARX and NKX2.1 orthologs) are also temporal factors. We show that Homeobrain and Scarecrow define middle-aged and late INP temporal windows and play a role in cellular longevity. Strikingly, Homeobrain and Scarecrow have conserved functions as temporal factors in the developing visual system. NanoDam enables rapid cell-type-specific genome-wide profiling with temporal resolution and is easily adapted for use in higher organisms.
神经祖细胞的时间模式是产生神经元多样性的一种进化保守策略。果蝇中枢大脑中的 II 型神经干细胞产生过渡扩增的中间神经祖细胞(INP),这些细胞表现出时间模式。然而,已知的时间因素并不能解释成年大脑中的神经元多样性。为了寻找缺失的因素,我们开发了 NanoDam,它可以通过一次遗传杂交,快速在体内对内源性标记蛋白进行全基因组分析。用 NanoDam 对已知时间转录因子的靶标进行作图,揭示了 Homeobrain 和 Scarecrow(ARX 和 NKX2.1 的同源物)也是时间因子。我们表明,Homeobrain 和 Scarecrow 定义了中年和晚期 INP 的时间窗口,并在细胞寿命中发挥作用。引人注目的是,Homeobrain 和 Scarecrow 在发育中的视觉系统中作为时间因子具有保守功能。NanoDam 能够以时间分辨率进行快速的细胞类型特异性全基因组分析,并且易于适应于高等生物。