Human phosphoglycerate dehydrogenase produces the oncometabolite D-2-hydroxyglutarate and promotes histone methylation
© Fan et al; licensee BioMed Central Ltd. 2014
Published: 28 May 2014
Materials and methods
To analyze the catalytic activity of PHGDH on possible alternative substrates, we conducted in vitro biochemical assays on recombinant human PHGDH. The reaction rate in the reductive direction with various substrates was monitored based on NADH consumption, measured by absorbance at 340 nm. The identity and chirality of products were analyzed by liquid chromatography-mass spectrometry (LC-MS) and by gas chromatography-mass spectrometry (GC-MS) after (R)-2-butanol derivatization. To analyze the intracellular function of PHGDH, we generated stable PHGDH knockdown cell lines, using two shRNA sequences. Metabolite levels in the knockdown cells were analyzed by LC-MS , and DNA and histone methylation was analyzed by immunoblotting.
Here we show that, in addition to catalyzing oxidation of 3-phosphoglycerate, PHGDH catalyzes NADH-dependent reduction of α-ketoglutarate to the oncometabolite D-2-hydroxyglutarate (D-2HG) and promotes histone methylation. The impact of PHGDH knockdown was studied in three cell lines with amplified PHGDH: MDA-MB-468, BT-20, and HCC70. Knockdown of PHGDH decreased 2HG levels in MDA-MB-468 and BT-20 cells, but not HCC70 cells (which had the highest 2HG levels of the three tested cell lines, with levels in MDA-MB-468 and BT-20 cells far below those found in cells with mutant IDH). These results suggest that PHGDH contributes to physiological 2HG pools, but may not produce high enough concentrations to cause pathology. Interestingly, in all three cell lines, PHGDH knockdown substantially decreased histone methylation. The mechanism underlying the decreased methylation upon PHGDH knockdown remains unclear, but it could be restored in MDA-MB-468 and BT-20 cells by addition of D-2HG ester.
PHGDH may promote histone methylation by mechanisms including 2-HG production.
- Mullarky E, Mattaini KR, Vander Heiden MG, Cantley LC, Locasale JW: PHGDH amplification and altered glucose metabolism in human melanoma. Pigment Cell Melanoma Res. 2011, 24: 1112-5. 10.1111/j.1755-148X.2011.00919.x.View ArticlePubMedGoogle Scholar
- Possemato R, et al: Functional genomics reveal that the serine synthesis pathway is essential in breast cancer. Nature. 2011, 476: 346-50. 10.1038/nature10350.PubMed CentralView ArticlePubMedGoogle Scholar
- Locasale JW, et al: Phosphoglycerate dehydrogenase diverts glycolytic flux and contributes to oncogenesis. Nat Genet. 2011, 43: 869-874. 10.1038/ng.890.PubMed CentralView ArticlePubMedGoogle Scholar
- Lu W, et al: Metabolomic analysis via reversed-phase ion-pairing liquid chromatography coupled to a stand alone orbitrap mass spectrometer. Anal Chem. 2010, 82: 3212-3221. 10.1021/ac902837x.PubMed CentralView ArticlePubMedGoogle Scholar
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