Mechanism of hsp70i Gene Bookmarking

Author:

Xing Hongyan12345,Wilkerson Donald C.12345,Mayhew Christopher N.12345,Lubert Eric J.12345,Skaggs Hollie S.12345,Goodson Michael L.12345,Hong Yiling12345,Park-Sarge Ok-Kyong12345,Sarge Kevin D.12345

Affiliation:

1. Department of Molecular and Cellular Biochemistry, Chandler Medical Center, University of Kentucky, Lexington, KY 40536, USA.

2. Department of Physiology, Chandler Medical Center, University of Kentucky, Lexington, KY 40536, USA.

3. Department of Cell Biology, Neurobiology, and Anatomy, University of Cincinnati, Cincinnati, OH 45267, USA.

4. Battelle Memorial Institute, Columbus, OH 43201, USA.

5. Section of Microbiology, University of California at Davis, Davis, CA 95616, USA.

Abstract

In contrast to most genomic DNA in mitotic cells, the promoter regions of some genes, such as the stress-inducible hsp70i gene that codes for a heat shock protein, remain uncompacted, a phenomenon called bookmarking. Here we show that hsp70i bookmarking is mediated by a transcription factor called HSF2, which binds this promoter in mitotic cells, recruits protein phosphatase 2A, and interacts with the CAP-G subunit of the condensin enzyme to promote efficient dephosphorylation and inactivation of condensin complexes in the vicinity, thereby preventing compaction at this site. Blocking HSF2-mediated bookmarking by HSF2 RNA interference decreases hsp70i induction and survival of stressed cells in the G 1 phase, which demonstrates the biological importance of gene bookmarking.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference26 articles.

1. T. Hirano, Cell Cycle3, 26 (2004).

2. A. V. Strunnikov, Prog. Cell Cycle Res.5, 361 (2003).

3. K. A. Hagstrom, B. J. Meyer, Nature Rev. Genet.4, 520 (2003).

4. The Making of the Mitotic Chromosome: Modern Insights into Classical Questions

5. K. Yokomori, Curr. Top. Microbiol. Immunol.274, 79 (2003).

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