کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
936727 1475188 2011 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
HDAC3 and the molecular brake pad hypothesis
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب رفتاری
پیش نمایش صفحه اول مقاله
HDAC3 and the molecular brake pad hypothesis
چکیده انگلیسی

Successful transcription of specific genes required for long-term memory processes involves the orchestrated effort of not only transcription factors, but also very specific enzymatic protein complexes that modify chromatin structure. Chromatin modification has been identified as a pivotal molecular mechanism underlying certain forms of synaptic plasticity and memory. The best-studied form of chromatin modification in the learning and memory field is histone acetylation, which is regulated by histone acetyltransferases and histone deacetylases (HDACs). HDAC inhibitors have been shown to strongly enhance long-term memory processes, and recent work has aimed to identify contributions of individual HDACs. In this review, we focus on HDAC3 and discuss its recently defined role as a negative regulator of long-term memory formation. HDAC3 is part of a corepressor complex and has direct interactions with Class II HDACs that may be important for its molecular and behavioral consequences. And last, we propose the “molecular brake pad” hypothesis of HDAC function. The HDACs and associated corepressor complexes may function in neurons, in part, as “molecular brake pads.” HDACs are localized to promoters of active genes and act as a persistent clamp that requires strong activity-dependent signaling to temporarily release these complexes (or brake pads) to activate gene expression required for long-term memory formation. Thus, HDAC inhibition removes the “molecular brake pads” constraining the processes necessary for long-term memory and results in strong, persistent memory formation.


► HDAC3 is part of a corepressor complex and has direct interactions with other HDACs.
► This interaction may be important for HDAC3’s molecular and behavioral consequence.
► We discuss HDAC3 function as a negative regulator of long-term memory formation.
► We propose the “molecular brake pad” hypothesis of HDAC function.
► HDACs and corepressor complexes may function in neurons as “molecular brake pads.”

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neurobiology of Learning and Memory - Volume 96, Issue 1, July 2011, Pages 27–34
نویسندگان
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