Influence of Metabolism on Epigenetics and Disease

被引:699
作者
Kaelin, William G., Jr. [1 ,2 ,3 ]
McKnight, Steven L. [4 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Boston, MA 02215 USA
[3] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
关键词
OFFSPRING DNA METHYLATION; ACETYL-COA SYNTHETASE; COMBINED FOLIC-ACID; HISTONE METHYLATION; OXIDATIVE STRESS; ONCOMETABOLITE; 2-HYDROXYGLUTARATE; S-ADENOSYLMETHIONINE; ESSENTIAL COFACTOR; TUMOR-SUPPRESSOR; GENE-EXPRESSION;
D O I
10.1016/j.cell.2013.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chemical modifications of histones and DNA, such as histone methylation, histone acetylation, and DNA methylation, play critical roles in epigenetic gene regulation. Many of the enzymes that add or remove such chemical modifications are known, or might be suspected, to be sensitive to changes in intracellular metabolism. This knowledge provides a conceptual foundation for understanding how mutations in the metabolic enzymes SDH, FH, and IDH can result in cancer and, more broadly, for how alterations in metabolism and nutrition might contribute to disease. Here, we review literature pertinent to hypothetical connections between metabolic and epigenetic states in eukaryotic cells.
引用
收藏
页码:56 / 69
页数:14
相关论文
共 127 条
[1]   Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies [J].
Abdel-Wahab, Omar ;
Mullally, Ann ;
Hedvat, Cyrus ;
Garcia-Manero, Guillermo ;
Patel, Jay ;
Wadleigh, Martha ;
Malinge, Sebastien ;
Yao, JinJuan ;
Kilpivaara, Outi ;
Bhat, Rukhmi ;
Huberman, Kety ;
Thomas, Sabrena ;
Dolgalev, Igor ;
Heguy, Adriana ;
Paietta, Elisabeth ;
Le Beau, Michelle M. ;
Beran, Miloslav ;
Tallman, Martin S. ;
Ebert, Benjamin L. ;
Kantarjian, Hagop M. ;
Stone, Richard M. ;
Gilliland, D. Gary ;
Crispino, John D. ;
Levine, Ross L. .
BLOOD, 2009, 114 (01) :144-147
[2]   Renal Cyst Formation in Fh1-Deficient Mice Is Independent of the Hif/Phd Pathway: Roles for Fumarate in KEAP1 Succination and Nrf2 Signaling [J].
Adam, Julie ;
Hatipoglu, Emine ;
O'Flaherty, Linda ;
Ternette, Nicola ;
Sahgal, Natasha ;
Lockstone, Helen ;
Baban, Dilair ;
Nye, Emma ;
Stamp, Gordon W. ;
Wolhuter, Kathryn ;
Stevens, Marcus ;
Fischer, Roman ;
Carmeliet, Peter ;
Maxwell, Patrick H. ;
Pugh, Chris W. ;
Frizzell, Norma ;
Soga, Tomoyoshi ;
Kessler, Benedikt M. ;
El-Bahrawy, Mona ;
Ratcliffe, Peter J. ;
Pollard, Patrick J. .
CANCER CELL, 2011, 20 (04) :524-537
[3]   Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2 [J].
Amary, M. Fernanda ;
Damato, Stephen ;
Halai, Dina ;
Eskandarpour, Malihe ;
Berisha, Fitim ;
Bonar, Fiona ;
McCarthy, Stan ;
Fantin, Valeria R. ;
Straley, Kimberly S. ;
Lobo, Samira ;
Aston, Will ;
Green, Claire L. ;
Gale, Rosemary E. ;
Tirabosco, Roberto ;
Futreal, Andrew ;
Campbell, Peter ;
Presneau, Nadege ;
Flanagan, Adrienne M. .
NATURE GENETICS, 2011, 43 (12) :1262-U129
[4]   B Vitamin and/or ω-3 Fatty Acid Supplementation and Cancer Ancillary Findings From the Supplementation With Folate, Vitamins B6 and B12, and/or Omega-3 Fatty Acids (SU.FOL.OM3) Randomized Trial [J].
Andreeva, Valentina A. ;
Touvier, Mathilde ;
Kesse-Guyot, Emmanuelle ;
Julia, Chantal ;
Galan, Pilar ;
Hercberg, Serge .
ARCHIVES OF INTERNAL MEDICINE, 2012, 172 (07) :540-547
[5]   Absolute metabolite concentrations and implied enzyme active site occupancy in Escherichia coli [J].
Bennett, Bryson D. ;
Kimball, Elizabeth H. ;
Gao, Melissa ;
Osterhout, Robin ;
Van Dien, Stephen J. ;
Rabinowitz, Joshua D. .
NATURE CHEMICAL BIOLOGY, 2009, 5 (08) :593-599
[6]   DNA methylation patterns and epigenetic memory [J].
Bird, A .
GENES & DEVELOPMENT, 2002, 16 (01) :6-21
[7]   On Acetyl-CoA as a Gauge of Cellular Metabolic State [J].
Cai, L. ;
Tu, B. P. .
METABOLISM AND DISEASE, 2011, 76 :195-202
[8]   Driving the Cell Cycle Through Metabolism [J].
Cai, Ling ;
Tu, Benjamin P. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 28, 2012, 28 :59-87
[9]   Acetyl-CoA Induces Cell Growth and Proliferation by Promoting the Acetylation of Histones at Growth Genes [J].
Cai, Ling ;
Sutter, Benjamin M. ;
Li, Bing ;
Tu, Benjamin P. .
MOLECULAR CELL, 2011, 42 (04) :426-437
[10]   SODIUM BUTYRATE INHIBITS HISTONE DEACETYLATION IN CULTURED-CELLS [J].
CANDIDO, EPM ;
REEVES, R ;
DAVIE, JR .
CELL, 1978, 14 (01) :105-113