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活性区蛋白SYD-2/Liprin-α在LRK-1/LRRK2下游发挥作用,通过网格蛋白衔接蛋白复合物调节突触小泡前体的极化运输。

Active zone protein SYD-2/Liprin- acts downstream of LRK-1/LRRK2 to regulate polarized trafficking of synaptic vesicle precursors through clathrin adaptor protein complexes.

作者信息

Nadiminti Sravanthi S P, Dixit Shirley B, Ratnakaran Neena, Hegde Sneha, Swords Sierra, Grant Barth D, Koushika Sandhya P

机构信息

Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, Maharashtra - 400 005, India.

Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854, USA.

出版信息

bioRxiv. 2023 Feb 26:2023.02.26.530068. doi: 10.1101/2023.02.26.530068.

Abstract

Synaptic vesicle proteins (SVps) are thought to travel in heterogeneous carriers dependent on the motor UNC-104/KIF1A. In neurons, we found that some SVps are transported along with lysosomal proteins by the motor UNC-104/KIF1A. LRK-1/LRRK2 and the clathrin adaptor protein complex AP-3 are critical for the separation of lysosomal proteins from SVp transport carriers. In mutants, both SVp carriers and SVp carriers containing lysosomal proteins are independent of UNC-104, suggesting that LRK-1 plays a key role in ensuring UNC-104-dependent transport of SVps. Additionally, LRK-1 likely acts upstream of the AP-3 complex and regulates the membrane localization of AP-3. The action of AP-3 is necessary for the active zone protein SYD-2/Liprin-α to facilitate the transport of SVp carriers. In the absence of the AP-3 complex, SYD-2/Liprin-α acts with UNC-104 to instead facilitate the transport of SVp carriers containing lysosomal proteins. We further show that the mistrafficking of SVps into the dendrite in and mutants depends on SYD-2, likely by regulating the recruitment of the AP-1/UNC-101. We propose that SYD-2 acts in concert with both the AP-1 and AP-3 complexes to ensure polarized trafficking of SVps.

摘要

突触小泡蛋白(SVps)被认为通过依赖于动力蛋白UNC-104/KIF1A的异质性载体运输。在神经元中,我们发现一些SVps与溶酶体蛋白一起由动力蛋白UNC-104/KIF1A运输。LRK-1/LRRK2和网格蛋白衔接蛋白复合物AP-3对于溶酶体蛋白与SVp运输载体的分离至关重要。在突变体中,SVp载体和含有溶酶体蛋白的SVp载体均不依赖于UNC-104,这表明LRK-1在确保SVps依赖UNC-104的运输中起关键作用。此外,LRK-1可能在AP-3复合物的上游起作用,并调节AP-3的膜定位。AP-3的作用对于活性区蛋白SYD-2/Liprin-α促进SVp载体的运输是必要的。在没有AP-3复合物的情况下,SYD-2/Liprin-α与UNC-104一起作用,反而促进了含有溶酶体蛋白的SVp载体的运输。我们进一步表明,在[具体突变体]突变体中SVps向树突的错误运输取决于SYD-2,可能是通过调节AP-1/UNC-101的募集。我们提出SYD-2与AP-1和AP-3复合物协同作用,以确保SVps的极化运输。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83b0/9980171/177b652006bc/nihpp-2023.02.26.530068v1-f0001.jpg

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