Götz Torsten W B, Puchkov Dmytro, Lysiuk Veronika, Lützkendorf Janine, Nikonenko Alexander G, Quentin Christine, Lehmann Martin, Sigrist Stephan J, Petzoldt Astrid G
Freie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.
Leibniz-Forschungsinstitut für Molekulare Pharmakologie im Forschungsverbund Berlin e.V., Campus Berlin-Buch, Berlin, Germany.
J Cell Biol. 2021 May 3;220(5). doi: 10.1083/jcb.202006040.
Reliable delivery of presynaptic material, including active zone and synaptic vesicle proteins from neuronal somata to synaptic terminals, is prerequisite for successful synaptogenesis and neurotransmission. However, molecular mechanisms controlling the somatic assembly of presynaptic precursors remain insufficiently understood. We show here that in mutants of the small GTPase Rab2, both active zone and synaptic vesicle proteins accumulated in the neuronal cell body at the trans-Golgi and were, consequently, depleted at synaptic terminals, provoking neurotransmission deficits. Ectopic presynaptic material accumulations consisted of heterogeneous vesicles and short tubules of 40 × 60 nm, segregating in subfractions either positive for active zone or synaptic vesicle proteins and LAMP1, a lysosomal membrane protein. Genetically, Rab2 acts upstream of Arl8, a lysosomal adaptor controlling axonal export of precursors. Collectively, we identified a Golgi-associated assembly sequence of presynaptic precursor biogenesis dependent on a Rab2-regulated protein export and sorting step at the trans-Golgi.
从神经元胞体向突触终末可靠地运输突触前物质,包括活性区和突触囊泡蛋白,是成功进行突触发生和神经传递的前提条件。然而,控制突触前前体在胞体组装的分子机制仍未得到充分了解。我们在此表明,在小GTP酶Rab2的突变体中,活性区和突触囊泡蛋白都在反式高尔基体处积聚在神经元细胞体中,因此在突触终末减少,引发神经传递缺陷。异位突触前物质积聚由40×60 nm的异质囊泡和短小管组成,在亚组分中分离,这些亚组分对活性区或突触囊泡蛋白以及溶酶体膜蛋白LAMP1呈阳性。在基因层面上,Rab2在Arl8的上游起作用,Arl8是一种控制前体轴突输出的溶酶体衔接蛋白。总的来说,我们确定了一种与高尔基体相关的突触前前体生物发生组装序列,该序列依赖于反式高尔基体处Rab2调节的蛋白质输出和分选步骤。