Product Detail
Product NameACSS2(Phospho-Ser659) Antibody
Host SpeciesRabbit
ClonalityPolyclonal
IsotypeIgG
ApplicationsWB
Species ReactivityHu Ms
Immunogen DescThe antiserum was produced against synthesized phosphopeptide derived from Human ACSS2 around the phosphorylation site of serine 659.
ConjugateUnconjugated
Calculated MW78kDa
StorageStore at -20℃/1 year
Application Details
WB dilution: 1:500-1:2000
Overcoming metabolic stress is a critical step in tumor growth. Acetyl coenzyme A (acetyl-CoA) generated from glucose and acetate uptake is important for his-tone acetylation and gene expression. However, how acetyl-CoA is produced under nutritional stress is un-clear. We demonstrate here that glucose deprivation results in AMP-activated protein kinase (AMPK)-medi-ated acetyl-CoA synthetase 2 (ACSS2) phosphoryla-tion at S659, which exposed the nuclear localization signal of ACSS2 for importin a5 binding and nuclear translocation. In the nucleus, ACSS2 binds to tran-scription factor EB and translocates to lysosomal and autophagy gene promoter regions, where ACSS2 incorporates acetate generated from histone acetylation turnover to locally produce acetyl-CoA for histone H3 acetylation in these regions and pro-mote lysosomal biogenesis, autophagy, cell survival, and brain tumorigenesis. In addition, ACSS2 S659 phosphorylation positively correlates with AMPK ac-tivity in glioma specimens and grades of glioma malig-nancy. These results underscore the significance of nuclear ACSS2-mediated histone acetylation in main-taining cell homeostasis and tumor development.
If you have published an article using product 58003, please notify us so that we can cite your literature.
et al,Targeting ACSS2 activity suspends the formation ofchemoresistance through suppressed histone H3acetylation in human breast cancer
, (2024),
PMID: