ACSS2
{{Short description|Protein-coding gene in the species Homo sapiens}}
{{Infobox_gene}}
Acyl-coenzyme A synthetase short-chain family member 2 is an enzyme that in humans is encoded by the ACSS2 gene.{{cite journal | vauthors = Luong A, Hannah VC, Brown MS, Goldstein JL | title = Molecular characterization of human acetyl-CoA synthetase, an enzyme regulated by sterol regulatory element-binding proteins | journal = The Journal of Biological Chemistry | volume = 275 | issue = 34 | pages = 26458–66 | date = August 2000 | pmid = 10843999 | doi = 10.1074/jbc.M004160200 | doi-access = free }}{{cite web | title = Entrez Gene: ACSS2 acyl-CoA synthetase short-chain family member 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55902}}
Function
This gene encodes a cytosolic enzyme 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 unsaturated fatty acids. Two transcript variants encoding different isoforms have been found for this gene.
Metabolic production of acetyl-CoA is linked to histone acetylation and gene regulation. In mouse neurons, Mews et al.{{cite journal | vauthors = Mews P, Donahue G, Drake AM, Luczak V, Abel T, Berger SL | title = Acetyl-CoA synthetase regulates histone acetylation and hippocampal memory | journal = Nature | date = May 2017 | pmid = 28562591 | doi = 10.1038/nature22405 | volume=546 | issue = 7658 | pmc=5505514 | pages=381–386| bibcode = 2017Natur.546..381M }} 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.{{cite journal | vauthors = Schmitt M, Matthies H | title = [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] | journal = Acta Biologica et Medica Germanica | volume = 38 | issue = 4 | pages = 683–9 | date = 1979 | pmid = 525146 }} Such acetylation correlates with the increased expression of a set of 'immediate early' genes,{{cite journal | vauthors = Peixoto L, Abel T | title = The role of histone acetylation in memory formation and cognitive impairments | journal = Neuropsychopharmacology | volume = 38 | issue = 1 | pages = 62–76 | date = January 2013 | pmid = 22669172 | pmc = 3521994 | doi = 10.1038/npp.2012.86 }} which encode proteins that broadly mediate changes in the strength of connections between neurons, therefore facilitating memory consolidation.{{cite journal | vauthors = West AE, Greenberg ME | title = Neuronal activity-regulated gene transcription in synapse development and cognitive function | journal = Cold Spring Harbor Perspectives in Biology | volume = 3 | issue = 6 | date = June 2011 | pmid = 21555405 | pmc = 3098681 | doi = 10.1101/cshperspect.a005744 | page=a005744}} 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
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11. Sabari BR, Tang Z, Huang H, Yong-Gonzalez V, Molina H, Kong HE, Dai L, Shimada M, Cross JR, Zhao Y, Roeder RG, Allis CD(2015). Intracellular crotonyl-CoA stimulates transcription through p300-catalyzed histone crotonylation. Mol Cell. 58(2):203-15
External links
- {{UCSC gene info|ACSS2}}
Further reading
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- {{cite journal | vauthors = Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T, Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K, Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T, Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T, Sugano S | title = Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes | journal = Genome Research | volume = 16 | issue = 1 | pages = 55–65 | date = January 2006 | pmid = 16344560 | pmc = 1356129 | doi = 10.1101/gr.4039406 }}
- {{cite journal | vauthors = Lehner B, Sanderson CM | title = A protein interaction framework for human mRNA degradation | journal = Genome Research | volume = 14 | issue = 7 | pages = 1315–23 | date = July 2004 | pmid = 15231747 | pmc = 442147 | doi = 10.1101/gr.2122004 }}
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