Department of Neurobiology, University of Chicago, Chicago, United States.
Committee on Neurobiology, University of Chicago, Chicago, United States.
Elife. 2020 Oct 1;9:e59464. doi: 10.7554/eLife.59464.
Terminal selectors are transcription factors (TFs) that establish during development and maintain throughout life post-mitotic neuronal identity. We previously showed that UNC-3/Ebf, the terminal selector of cholinergic motor neurons (MNs), acts indirectly to prevent alternative neuronal identities (Feng et al., 2020). Here, we globally identify the direct targets of UNC-3. Unexpectedly, we find that the suite of UNC-3 targets in MNs is modified across different life stages, revealing 'temporal modularity' in terminal selector function. In all larval and adult stages examined, UNC-3 is required for continuous expression of various protein classes (e.g. receptors, transporters) critical for MN function. However, only in late larvae and adults, UNC-3 is required to maintain expression of MN-specific TFs. Minimal disruption of UNC-3's temporal modularity via genome engineering affects locomotion. Another terminal selector (UNC-30/Pitx) also exhibits temporal modularity, supporting the potential generality of this mechanism for the control of neuronal identity.
终端选择器是转录因子(TFs),它们在发育过程中建立,并在有丝分裂后维持整个生命过程中的神经元身份。我们之前曾表明,UNC-3/Ebf 是 胆碱能运动神经元 (MNs) 的终端选择器,它间接作用以防止替代神经元身份(Feng 等人,2020 年)。在这里,我们全局鉴定了 UNC-3 的直接靶标。出乎意料的是,我们发现 MNs 中 UNC-3 的靶标套件在不同的生命阶段发生了改变,揭示了终端选择器功能的“时间模块化”。在所有检查的幼虫和成虫阶段,UNC-3 都需要持续表达各种对 MN 功能至关重要的蛋白质类(例如受体、转运蛋白)。然而,只有在晚期幼虫和成虫中,UNC-3 才需要维持 MN 特异性 TF 的表达。通过基因组工程对 UNC-3 的时间模块化进行最小的干扰会影响运动。另一个 终端选择器(UNC-30/Pitx)也表现出时间模块化,支持这种机制用于控制神经元身份的潜在普遍性。