McCormick Laura E, Barker Natalie K, Herring Laura E, Gupton Stephanie L
Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
Michael Hooker Proteomics Core, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
bioRxiv. 2024 Jan 6:2024.01.05.574385. doi: 10.1101/2024.01.05.574385.
The E3 ubiquitin ligase TRIM67 is enriched in the central nervous system and is required for proper neuronal development. Previously we demonstrated TRIM67 coordinates with the closely related E3 ubiquitin ligase TRIM9 to regulate cytoskeletal dynamics downstream of the netrin-1 during axon guidance and axon branching in early neuronal morphogenesis. Interestingly, loss of impacts cognitive flexibility in a spatial learning and memory task. Despite this behavioral phenotype, it was previously uninvestigated if TRIM67 was involved in synapse formation or function. Here we demonstrate TRIM67 localizes to the post-synaptic density (PSD) within dendritic spines. Furthermore, we show that loss of significantly changes the PSD proteome, including changes in the regulation of the actin and microtubule cytoskeletons. Collectively, our data propose a synaptic role for TRIM67.
E3泛素连接酶TRIM67在中枢神经系统中富集,是神经元正常发育所必需的。此前我们证明,在早期神经元形态发生过程中的轴突导向和轴突分支过程中,TRIM67与密切相关的E3泛素连接酶TRIM9协同作用,以调节netrin-1下游的细胞骨架动力学。有趣的是,TRIM67的缺失会影响空间学习和记忆任务中的认知灵活性。尽管有这种行为表型,但此前尚未研究TRIM67是否参与突触形成或功能。在这里,我们证明TRIM67定位于树突棘内的突触后致密区(PSD)。此外,我们表明TRIM67的缺失显著改变了PSD蛋白质组,包括肌动蛋白和微管细胞骨架调节的变化。总体而言,我们的数据表明TRIM67具有突触作用。