Sipa1l3/SPAR3 is targeted to postsynaptic specializations and interacts with the Fezzin ProSAPiP1/Lzts3

作者: Anna Dolnik , Noreen Kanwal , Sarah Mackert , Sonja Halbedl , Christian Proepper

DOI: 10.1111/JNC.13353

关键词:

摘要: Rap GTPase-activating proteins (RapGAPs) are essential for synaptic function as they tightly regulate signaling. Among the most abundant RapGAPs in brain Spine-associated (SPARs) Sipa1l1/SPAR and Sipa1l2/SPAR2, whereas nothing has been reported on Sipa1l3/SPAR3. In this study, we show that Sipa1l3/SPAR3 is conserved across species, a distinct expression pattern developing rat localized at excitatory postsynapses. We further demonstrate C-terminus required postsynaptic targeting represents an interaction module Fezzins such ProSAPiP1/Lzts3, binding partner of scaffold protein Shank3. Taken together, our data imply hitherto unknown RapGAP, which targeted to specializations interacts with Fezzins. modulators Our study first characterize SPAR family member neuronal tissue. postsynapses via its C-terminus, other including Fezzin ProSAPiP1/Lzts3.

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