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Cell Rep DOI:10.1016/j.celrep.2017.09.045

Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and Intelligence.

Publication TypeJournal Article
Year of Publication2017
AuthorsFernández, E, Collins, MO, Frank, RAW, Zhu, F, Kopanitsa, MV, Nithianantharajah, J, Lemprière, SA, Fricker, D, Elsegood, KA, McLaughlin, CL, Croning, MDR, Mclean, C, J Armstrong, D, W Hill, D, Deary, IJ, Cencelli, G, Bagni, C, Fromer, M, Purcell, SM, Pocklington, AJ, Choudhary, JS, Komiyama, NH, Grant, SGN
JournalCell Rep
Volume21
Issue3
Pages679-691
Date Published2017 Oct 17
ISSN2211-1247
Abstract

Arc is an activity-regulated neuronal protein, but little is known about its interactions, assembly into multiprotein complexes, and role in human disease and cognition. We applied an integrated proteomic and genetic strategy by targeting a tandem affinity purification (TAP) tag and Venus fluorescent protein into the endogenous Arc gene in mice. This allowed biochemical and proteomic characterization of native complexes in wild-type and knockout mice. We identified many Arc-interacting proteins, of which PSD95 was the most abundant. PSD95 was essential for Arc assembly into 1.5-MDa complexes and activity-dependent recruitment to excitatory synapses. Integrating human genetic data with proteomic data showed that Arc-PSD95 complexes are enriched in schizophrenia, intellectual disability, autism, and epilepsy mutations and normal variants in intelligence. We propose that Arc-PSD95 postsynaptic complexes potentially affect human cognitive function.

DOI10.1016/j.celrep.2017.09.045
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/29045836?dopt=Abstract

Alternate JournalCell Rep
PubMed ID29045836