A Topoisomerase IIß-Mediated dsDNA Break Required for Regulated Transcription

Author:

Ju Bong-Gun123,Lunyak Victoria V.123,Perissi Valentina123,Garcia-Bassets Ivan123,Rose David W.123,Glass Christopher K.123,Rosenfeld Michael G.123

Affiliation:

1. Howard Hughes Medical Institute, Department of Medicine, School of Medicine, 9500 Gilman Drive, University of California, San Diego, La Jolla, CA 92093–0648, USA.

2. Department of Medicine, Division of Endocrinology, School of Medicine, 9500 Gilman Drive, University of California, San Diego, La Jolla, CA 92093–0648, USA.

3. Department of Cellular and Molecular Medicine, School of Medicine, 9500 Gilman Drive, University of California, San Diego, La Jolla, CA 92093–0648, USA.

Abstract

Multiple enzymatic activities are required for transcriptional initiation. The enzyme DNA topoisomerase II associates with gene promoter regions and can generate breaks in double-stranded DNA (dsDNA). Therefore, it is of interest to know whether this enzyme is critical for regulated gene activation. We report that the signal-dependent activation of gene transcription by nuclear receptors and other classes of DNA binding transcription factors, including activating protein 1, requires DNA topoisomerase IIβ-dependent, transient, site-specific dsDNA break formation. Subsequent to the break, poly(adenosine diphosphate–ribose) polymerase–1 enzymatic activity is induced, which is required for a nucleosome-specific histone H1–high-mobility group B exchange event and for local changes of chromatin architecture. Our data mechanistically link DNA topoisomerase IIβ–dependent dsDNA breaks and the components of the DNA damage and repair machinery in regulated gene transcription.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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