| Literature DB >> 20178993 |
Yi Li1, Jie Hu, Klemens Höfer, Andrew M S Wong, Jonathan D Cooper, Shari G Birnbaum, Robert E Hammer, Sandra L Hofmann.
Abstract
A family of integral membrane proteins containing a signature DHHC motif has been shown to display protein S-acyltransferase activity, modifying cysteine residues in proteins with fatty acids. The physiological roles of these proteins have largely been unexplored. Here we report that mice homozygous for a hypomorphic allele of a previously uncharacterized member, DHHC5, are born at half the expected rate, and survivors show a marked deficit in contextual fear conditioning, an indicator of defective hippocampal-dependent learning. DHHC5 is highly enriched in a post-synaptic density preparation and co-immunoprecipitates with post-synaptic density protein-95 (PSD-95), an interaction that is mediated through binding of the carboxyl terminus of DHHC5 and the PDZ3 domain of PSD-95. Immunohistochemistry demonstrated that DHHC5 is expressed in the CA3 and dentate gyrus in the hippocampus. These findings point to a previously unsuspected role for DHHC5 in post-synaptic function affecting learning and memory.Entities:
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Year: 2010 PMID: 20178993 PMCID: PMC2857114 DOI: 10.1074/jbc.M109.079426
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157