Matches in SemOpenAlex for { <https://semopenalex.org/work/W2104496885> ?p ?o ?g. }
- W2104496885 endingPage "607" @default.
- W2104496885 startingPage "591" @default.
- W2104496885 abstract "The modification of intracellular proteins by monosaccharides of O-linked β-N-acetylglucosamine (O-GlcNAc) is an essential and dynamic PTM of metazoans. The addition and removal of O-GlcNAc is catalyzed by the O-GlcNAc transferase (OGT) and O-GlcNAcase, respectively. One mechanism by which O-GlcNAc is thought to mediate proteins is by regulating phosphorylation. To provide insight into the pathways regulated by O-GlcNAc, we have utilized SILAC-based quantitative proteomics to carry out comparisons of site-specific phosphorylation in OGT wild-type and Null cells. Quantitation of the phosphoproteome demonstrated that of 5529 phosphoserine, phosphothreonine, and phosphotyrosine sites, 232 phosphosites were upregulated and 133 downregulated in the absence of O-GlcNAc. Collectively, these data suggest that deletion of OGT has a profound effect on the phosphorylation of cell cycle and DNA damage response proteins. Key events were confirmed by biochemical analyses and demonstrate an increase in the activating autophosphorylation event on ATM (Ser1987) and on ATM's downstream targets p53, H2AX, and Chk2. Together, these data support widespread changes in the phosphoproteome upon removal of O-GlcNAc, suggesting that O-GlcNAc regulates processes such as the cell cycle, genomic stability, and lysosomal biogenesis. All MS data have been deposited in the ProteomeXchange with identifier PXD001153 (http://proteomecentral.proteomexchange.org/dataset/PXD001153)." @default.
- W2104496885 created "2016-06-24" @default.
- W2104496885 creator A5015933395 @default.
- W2104496885 creator A5020466456 @default.
- W2104496885 creator A5024268602 @default.
- W2104496885 creator A5028529518 @default.
- W2104496885 creator A5031609748 @default.
- W2104496885 creator A5034978906 @default.
- W2104496885 creator A5037945413 @default.
- W2104496885 creator A5049888866 @default.
- W2104496885 creator A5054278526 @default.
- W2104496885 creator A5073644538 @default.
- W2104496885 creator A5082936160 @default.
- W2104496885 date "2015-01-01" @default.
- W2104496885 modified "2023-10-16" @default.
- W2104496885 title "Quantitative phosphoproteomics reveals crosstalk between phosphorylation and<i>O</i>-GlcNAc in the DNA damage response pathway" @default.
- W2104496885 cites W1521417371 @default.
- W2104496885 cites W1553367038 @default.
- W2104496885 cites W1568866400 @default.
- W2104496885 cites W1970965314 @default.
- W2104496885 cites W1974667981 @default.
- W2104496885 cites W1978727038 @default.
- W2104496885 cites W1981194148 @default.
- W2104496885 cites W1983218764 @default.
- W2104496885 cites W1987345634 @default.
- W2104496885 cites W2004914600 @default.
- W2104496885 cites W2006296741 @default.
- W2104496885 cites W2007131458 @default.
- W2104496885 cites W2012232758 @default.
- W2104496885 cites W2016015885 @default.
- W2104496885 cites W2018507091 @default.
- W2104496885 cites W2022428368 @default.
- W2104496885 cites W2022811243 @default.
- W2104496885 cites W2025379444 @default.
- W2104496885 cites W2031087463 @default.
- W2104496885 cites W2033982929 @default.
- W2104496885 cites W2036321220 @default.
- W2104496885 cites W2041967294 @default.
- W2104496885 cites W2044013267 @default.
- W2104496885 cites W2049020770 @default.
- W2104496885 cites W2050149304 @default.
- W2104496885 cites W2051948190 @default.
- W2104496885 cites W2054664745 @default.
- W2104496885 cites W2060799932 @default.
- W2104496885 cites W2062238060 @default.
- W2104496885 cites W2062284662 @default.
- W2104496885 cites W2066108933 @default.
- W2104496885 cites W2068663943 @default.
- W2104496885 cites W2068805128 @default.
- W2104496885 cites W2069052453 @default.
- W2104496885 cites W2072135796 @default.
- W2104496885 cites W2072235312 @default.
- W2104496885 cites W2075375055 @default.
- W2104496885 cites W2080380725 @default.
- W2104496885 cites W2080752012 @default.
- W2104496885 cites W2083839424 @default.
- W2104496885 cites W2084089807 @default.
- W2104496885 cites W2085677500 @default.
- W2104496885 cites W2089723647 @default.
- W2104496885 cites W2091787667 @default.
- W2104496885 cites W2092938957 @default.
- W2104496885 cites W2095223090 @default.
- W2104496885 cites W2098425296 @default.
- W2104496885 cites W2099255819 @default.
- W2104496885 cites W2100521311 @default.
- W2104496885 cites W2105548732 @default.
- W2104496885 cites W2111768081 @default.
- W2104496885 cites W2129777487 @default.
- W2104496885 cites W2133465414 @default.
- W2104496885 cites W2133631672 @default.
- W2104496885 cites W2137404591 @default.
- W2104496885 cites W2137741805 @default.
- W2104496885 cites W2154885060 @default.
- W2104496885 cites W2157918066 @default.
- W2104496885 cites W2158217645 @default.
- W2104496885 cites W2158227421 @default.
- W2104496885 cites W2158841256 @default.
- W2104496885 cites W2168223461 @default.
- W2104496885 cites W2168386087 @default.
- W2104496885 cites W2170127671 @default.
- W2104496885 cites W2172268272 @default.
- W2104496885 doi "https://doi.org/10.1002/pmic.201400339" @default.
- W2104496885 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4564869" @default.
- W2104496885 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25263469" @default.
- W2104496885 hasPublicationYear "2015" @default.
- W2104496885 type Work @default.
- W2104496885 sameAs 2104496885 @default.
- W2104496885 citedByCount "53" @default.
- W2104496885 countsByYear W21044968852015 @default.
- W2104496885 countsByYear W21044968852016 @default.
- W2104496885 countsByYear W21044968852017 @default.
- W2104496885 countsByYear W21044968852018 @default.
- W2104496885 countsByYear W21044968852019 @default.
- W2104496885 countsByYear W21044968852020 @default.
- W2104496885 countsByYear W21044968852021 @default.
- W2104496885 countsByYear W21044968852022 @default.
- W2104496885 countsByYear W21044968852023 @default.
- W2104496885 crossrefType "journal-article" @default.