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Articles

p53 Chromatin Epigenetic Domain Organization and p53 Transcription

Chia-Hsin Su, Yih-Jyh Shann, Ming-Ta Hsu
Chia-Hsin Su
1Institute of Biochemistry and Molecular Biology, School of Life Science
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Yih-Jyh Shann
1Institute of Biochemistry and Molecular Biology, School of Life Science
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Ming-Ta Hsu
1Institute of Biochemistry and Molecular Biology, School of Life Science
2Genome Research Center, National Yang Ming University, Taipei 11221, Taiwan, Republic of China
3Chien-Tien Hsu Cancer Research Foundation, Taipei, Taiwan, Republic of China
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  • For correspondence: mth@ym.edu.tw
DOI: 10.1128/MCB.00704-08
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ABSTRACT

Epigenetic organization represents an important regulation mechanism of gene expression. In this work, we show that the mouse p53 gene is organized into two epigenetic domains. The first domain is fully unmethylated, associated with histone modifications in active genes, and organized in a nucleosome-free conformation that is deficient in H2a/H2b, whereas the second domain is fully methylated, associated with deacetylated histones, and organized in a nucleosomal structure. In mitotic cells, RNA polymerase is depleted in domain II, which is folded into a higher-order structure and is associated with H1 histone, whereas domain I conformation is preserved. Similar results were obtained for cells treated with inhibitors of associated regulatory factors. These results suggest that depletion of RNA polymerase II is the result of a physical barrier due to the folding of chromatin in domain II. The novel chromatin structure in the first domain during mitosis also suggests a mechanism for marking active genes in successive cell cycles.

  • Copyright © 2009 American Society for Microbiology
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p53 Chromatin Epigenetic Domain Organization and p53 Transcription
Chia-Hsin Su, Yih-Jyh Shann, Ming-Ta Hsu
Molecular and Cellular Biology Dec 2008, 29 (1) 93-103; DOI: 10.1128/MCB.00704-08

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p53 Chromatin Epigenetic Domain Organization and p53 Transcription
Chia-Hsin Su, Yih-Jyh Shann, Ming-Ta Hsu
Molecular and Cellular Biology Dec 2008, 29 (1) 93-103; DOI: 10.1128/MCB.00704-08
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KEYWORDS

chromatin
Epigenesis, Genetic
Transcription, Genetic
Tumor Suppressor Protein p53

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