This gene encodes a cytosolicenzyme that catalyzes the activation of acetate for use in lipid synthesis and energy generation. The protein acts as a monomer and produces acetyl-CoA from acetate in a reaction that requires ATP. It is also essential for the production of Crotonyl-CoA which activates its target genes by crotonylation of histone tails. Expression of this gene is regulated by sterol regulatory element-binding proteins, transcription factors that activate genes required for the synthesis of cholesterol and unsaturatedfatty acids. Two transcript variants encoding different isoforms have been found for this gene.[2]
Metabolic production of acetyl-CoA is linked to histone acetylation and gene regulation. In mouse neurons, Mews et al.[3] identified a major role for the ACSS2 pathway to regulate histone acetylation and neuronal gene expression. Histone acetylation in mature neurons is associated strongly with memory formation. Chromatin becomes acetylated in specific regions of the brain, such as the hippocampus, in response to neuronal activity or behavioral training in rodent.[4] Such acetylation correlates with the increased expression of a set of 'immediate early' genes,[5] which encode proteins that broadly mediate changes in the strength of connections between neurons, therefore facilitating memory consolidation.[6] In the mouse hippocampus, ACSS2 binds directly to immediate early genes to 'fuel' local histone acetylation and, in turn, their induction for long-term spatial memory.
References
↑Luong A, Hannah VC, Brown MS, Goldstein JL (August 2000). "Molecular characterization of human acetyl-CoA synthetase, an enzyme regulated by sterol regulatory element-binding proteins". The Journal of Biological Chemistry. 275 (34): 26458–66. doi:10.1074/jbc.M004160200. PMID10843999.
↑Schmitt M, Matthies H (1979). "[Biochemical studies on histones of the central nervous system. III. Incorporation of [14C]-acetate into the histones of different rat brain regions during a learning experiment]". Acta Biologica et Medica Germanica. 38 (4): 683–9. PMID525146.
