Activation of proto-oncogenes by disruption of chromosome neighborhoods

Author:

Hnisz Denes1,Weintraub Abraham S.12,Day Daniel S.1,Valton Anne-Laure3,Bak Rasmus O.4,Li Charles H.12,Goldmann Johanna1,Lajoie Bryan R.3,Fan Zi Peng15,Sigova Alla A.1,Reddy Jessica12,Borges-Rivera Diego12,Lee Tong Ihn1,Jaenisch Rudolf12,Porteus Matthew H.4,Dekker Job36,Young Richard A.12

Affiliation:

1. Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.

2. Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

3. Program in Systems Biology, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

4. Department of Pediatrics, Stanford University, Stanford, CA, USA.

5. Computational and Systems Biology Program, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

6. Howard Hughes Medical Institute.

Abstract

The spread of bad neighborhoods Our genomes have complex three-dimensional (3D) arrangements that partition and regulate gene expression. Cancer cells frequently have their genomes grossly rearranged, disturbing this intricate 3D organization. Hnisz et al. show that the disruption of these 3D neighborhoods can bring oncogenes under the control of regulatory elements normally kept separate from them (see the Perspective by Wala and Beroukim). These novel juxtapositions can result in the inappropriate activation of oncogenes. Science , this issue p. 1454 ; see also p. 1398

Funder

Austrian Science Fund

Ludwig Graduate Fellowship

Laurie Kraus Lacob Faculty Scholar Award in Pediatric Translational Research

Hyundai Hope on Wheels

Danish Council for Independent Research, Medical Sciences

Sapere Aude Research Talent

National Human Genome Research Institute

National Cancer Institute

NIH

National Institute of General Medical Sciences

National Institute of Allergy and Infectious Diseases

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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