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在 MARK2 信号的作用下,通过 KIF3/KAP3/TRIM46 运输实现轴突起始段的时空构建。

The Spatiotemporal Construction of the Axon Initial Segment via KIF3/KAP3/TRIM46 Transport under MARK2 Signaling.

机构信息

Department of Cell Biology and Anatomy, Graduate School of Medicine, University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

Department of Cell Biology and Anatomy, Graduate School of Medicine, University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan; Center of Excellence in Genome Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia.

出版信息

Cell Rep. 2019 Aug 27;28(9):2413-2426.e7. doi: 10.1016/j.celrep.2019.07.093.

Abstract

The axon initial segment (AIS) is a compartment that serves as a molecular barrier to achieve axon-dendrite differentiation. Distribution of specific proteins during early neuronal development has been proposed to be critical for AIS construction. However, it remains unknown how these proteins are specifically targeted to the proximal axon within this limited time period. Here, we reveal spatiotemporal regulation driven by the microtubule (MT)-based motor KIF3A/B/KAP3 that transports TRIM46, influenced by a specific MARK2 phosphorylation cascade. In the proximal part of the future axon under low MARK2 activity, the KIF3/KAP3 motor recognizes TRIM46 as cargo and transports it to the future AIS. In contrast, in the somatodendritic area under high MARK2 activity, KAP3 phosphorylated at serine 60 by MARK2 cannot bind with TRIM46 and be transported. This spatiotemporal regulation between KIF3/KAP3 and TRIM46 under specific MARK2 activity underlies the specific transport needed for axonal differentiation.

摘要

轴突起始段(AIS)是作为分子屏障的隔室,以实现轴突-树突分化。早期神经元发育过程中特定蛋白质的分布被认为对 AIS 的构建至关重要。然而,目前尚不清楚这些蛋白质如何在这段有限的时间内特异性地靶向近端轴突。在这里,我们揭示了由微管(MT)基马达 KIF3A/B/KAP3 驱动的时空调节,该调节受特定 MARK2 磷酸化级联的影响。在未来轴突的近端部分,MARK2 活性较低时,KIF3/KAP3 马达将 TRIM46 识别为货物并将其运输到未来的 AIS。相比之下,在 MARK2 活性较高的树突体区域,被 MARK2 磷酸化 Ser60 的 KAP3 不能与 TRIM46 结合并被运输。这种在特定 MARK2 活性下 KIF3/KAP3 和 TRIM46 之间的时空调节是轴突分化所需的特异性运输的基础。

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