Bradley E. Bernstein, M.D., Ph.D.

Bradley Bernstein, M.D., Ph.D.

Chair of Cancer Biology (Dana-Farber Cancer Institute)
Richard and Nancy Lubin Family Chair (DFCI)
Professor of Pathology (HMS)
Professor of Cell Biology (HMS)
LC-8313, 450 Brookline Avenue

Bradley Bernstein, M.D., Ph.D. is the Chair of Cancer Biology at the Dana-Farber Cancer Institute, where he holds the Richard and Nancy Lubin Family Chair. He is also the Director of the Gene Regulation Observatory at the Broad Institute, a Professor of Pathology and a Professor of Cell Biology at Harvard Medical School, and an Investigator in Harvard’s Ludwig Institute.

Dr. Bernstein’s research focuses on epigenetic gene regulation. The Bernstein Lab studies how gene activity is controlled by noncoding regulatory elements such as ‘enhancers’, and by the way the genes are packaged into chromatin. His work is notable for the discovery of ‘bivalent domains’, a signature chromatin state consisting of opposing histone modifications that poise master genes for alternate fates. His characterization of bivalent chromatin and associated regulatory factors in stem cells was a key early demonstration of the mechanistic impact of chromatin on mammalian development. His subsequent work as a leader of the NIH’s ENCODE consortium revealed that the vast ‘noncoding’ portions of the human genome, which had previously been dismissed as ‘junk’, are in fact packed with sequence elements that control gene activity.

Dr. Bernstein’s second major area of contribution is cancer epigenetics. He showed that DNA methylation can activate oncogenes by disrupting genomic insulators, an entirely unexpected discovery given that methylation had been so closely tied to repression. This finding explains how certain tumors can sustain potent oncogenic signaling in the absence of canonical mutations. His group has also uncovered epigenetic mechanisms that underlie tumor cell self-renewal, drug tolerance and immune evasion.

Dr. Bernstein received his B.S. from Yale University in 1992 and his M.D. and Ph.D. from the University of Washington in 1999, before completing a residency in clinical pathology at Brigham and Women’s Hospital and postdoctoral research at Harvard University.

Dana-Farber Cancer Institute

Cancer Biology/LC-8313

450 Brookline Avenue

Boston, MA 02215

Office: 617-632-5160

Global nucleosome occupancy in yeast.
Authors: Authors: Bernstein BE, Liu CL, Humphrey EL, Perlstein EO, Schreiber SL.
Genome Biol
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The use of chromatin immunoprecipitation assays in genome-wide analyses of histone modifications.
Authors: Authors: Bernstein BE, Humphrey EL, Liu CL, Schreiber SL.
Methods Enzymol
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Methylation of histone H3 K4 mediates association of the Isw1p ATPase with chromatin.
Authors: Authors: Santos-Rosa H, Schneider R, Bernstein BE, Karabetsou N, Morillon A, Weise C, Schreiber SL, Mellor J, Kouzarides T.
Mol Cell
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Development and validation of a T7 based linear amplification for genomic DNA.
Authors: Authors: Liu CL, Schreiber SL, Bernstein BE.
BMC Genomics
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Signaling network model of chromatin.
Authors: Authors: Schreiber SL, Bernstein BE.
Cell
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Global approaches to chromatin.
Authors: Authors: Bernstein BE, Schreiber SL.
Chem Biol
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Active genes are tri-methylated at K4 of histone H3.
Authors: Authors: Santos-Rosa H, Schneider R, Bannister AJ, Sherriff J, Bernstein BE, Emre NC, Schreiber SL, Mellor J, Kouzarides T.
Nature
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Methylation of histone H3 Lys 4 in coding regions of active genes.
Authors: Authors: Bernstein BE, Humphrey EL, Erlich RL, Schneider R, Bouman P, Liu JS, Kouzarides T, Schreiber SL.
Proc Natl Acad Sci U S A
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SEMAPHORE1 functions during the regulation of ancestrally duplicated knox genes and polar auxin transport in maize.
Authors: Authors: Scanlon MJ, Henderson DC, Bernstein B.
Development
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Genomewide studies of histone deacetylase function in yeast.
Authors: Authors: Bernstein BE, Tong JK, Schreiber SL.
Proc Natl Acad Sci U S A
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