Department of Cellular and Physiological Sciences, University of British Columbia, Vancouver, British Columbia, V6T 1Z3, Canada.
Spemann Graduate School of Biology and Medicine (SGBM), University of Freiburg, Freiburg, 79104, Germany.
Nucleic Acids Res. 2022 Sep 23;50(17):9748-9764. doi: 10.1093/nar/gkac730.
Retrograde bone morphogenetic protein (BMP) signaling at the Drosophila neuromuscular junction (NMJ) has served as a paradigm to study TGF-β-dependent synaptic function and maturation. Yet, how retrograde BMP signaling transcriptionally regulates these functions remains unresolved. Here, we uncover a gene network, enriched for neurotransmission-related genes, that is controlled by retrograde BMP signaling in motor neurons through two Smad-binding cis-regulatory motifs, the BMP-activating (BMP-AE) and silencer (BMP-SE) elements. Unpredictably, both motifs mediate direct gene activation, with no involvement of the BMP derepression pathway regulators Schnurri and Brinker. Genome editing of candidate BMP-SE and BMP-AE within the locus of the active zone gene bruchpilot, and a novel Ly6 gene witty, demonstrated the role of these motifs in upregulating genes required for the maturation of pre- and post-synaptic NMJ compartments. Our findings uncover how Smad-dependent transcriptional mechanisms specific to motor neurons directly orchestrate a gene network required for synaptic maturation by retrograde BMP signaling.
果蝇神经肌肉接头(NMJ)中的逆行骨形态发生蛋白(BMP)信号转导已成为研究 TGF-β 依赖性突触功能和成熟的范例。然而,逆行 BMP 信号如何在转录水平上调节这些功能仍未解决。在这里,我们揭示了一个基因网络,该网络富含与神经传递相关的基因,通过两个 Smad 结合顺式调节元件,即 BMP 激活(BMP-AE)和沉默(BMP-SE)元件,逆行 BMP 信号在运动神经元中对其进行调控。出人意料的是,这两个基序都介导了直接的基因激活,而不涉及 BMP 去抑制途径调节剂 Schnurri 和 Brinker。在活性区基因 bruchpilot 和一个新的 Ly6 基因 witty 内对候选 BMP-SE 和 BMP-AE 进行基因组编辑,证明了这些基序在上调成熟前和成熟后 NMJ 区所必需的基因中的作用。我们的研究结果揭示了运动神经元中特有的 Smad 依赖性转录机制如何通过逆行 BMP 信号直接协调一个对突触成熟所必需的基因网络。