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A putative tyrosine phosphorylation site of the cell surface receptor golden goal is involved in synaptic layer selection in the visual system

机译:细胞表面受体黄金靶点的酪氨酸磷酸化位点参与视觉系统突触层的选择

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Golden goal (Gogo) is a cell surface protein that is crucial for proper synaptic layer targeting of photoreceptors (R cells) in the Drosophila visual system. In collaboration with the seven-transmembrane cadherin Flamingo (Fmi), Gogo mediates both temporary and final layer targeting of R-cell axons through its cytoplasmic activity. However, it is not known how Gogo activity is regulated. Here, we show that a conserved Tyr-Tyr-Asp (YYD) tripeptide motif in the Gogo cytoplasmic domain is required for photoreceptor axon targeting. Deleting the YYD motif is sufficient to abolish Gogo function. We demonstrate that the YYD motif is a phosphorylation site and that mutations in the YYD tripeptide impair synaptic layer targeting. Gogo phosphorylation results in axon stopping at the temporary targeting layer, and dephosphorylation is crucial for final layer targeting in collaboration with Fmi. Therefore, both temporary and final layer targeting strongly depend on the Gogo phosphorylation status. Drosophila Insulin-like receptor (DInR) has been reported to regulate the wiring of photoreceptors. We show that insulin signaling is a positive regulator, directly or indirectly, of YYD motif phosphorylation. Our findings indicate a novel mechanism for the regulation of Gogo activity by insulin signaling-mediated phosphorylation. We propose the model that a constant phosphorylation signal is antagonized by a presumably temporal dephosphorylation signal, which creates a permissive signal that controls developmental timing in axon targeting.
机译:金色目标(Gogo)是一种细胞表面蛋白,对于果蝇视觉系统中的感光细胞(R细胞)的正确突触层靶向至关重要。与七跨膜钙粘蛋白火烈鸟(Fmi)合作,Gogo通过其细胞质活性介导了R细胞轴突的临时和最终层靶向。但是,尚不知道如何调节Gogo活动。在这里,我们表明,在感光细胞轴突靶向Gogo胞质域中的保守的Tyr-Tyr-Asp(YYD)三肽基序是必需的。删除YYD主题足以取消Gogo功能。我们证明YYD母题是一个磷酸化位点,并且YYD三肽中的突变会损害突触层靶向。 Gogo磷酸化导致轴突停止在临时靶向层,而去磷酸化对于与Fmi合作对最终靶向层至关重要。因此,临时和最终目标层都强烈依赖于Gogo磷酸化状态。果蝇胰岛素样受体(DInR)已被报道来调节感光器的布线。我们显示,胰岛素信号传导是YYD基序磷酸化的直接或间接的正调节剂。我们的发现表明通过胰岛素信号介导的磷酸化调节Gogo活性的新机制。我们提出了一个模型,即恒定的磷酸化信号被可能是暂时的去磷酸化信号所拮抗,该信号会产生一个允许的信号,该信号控制轴突靶向的发育时机。

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