Title of article
Hdac3 Is Essential for the Maintenance of Chromatin Structure and Genome Stability
Author/Authors
Bhaskara، نويسنده , , Srividya and Knutson، نويسنده , , Sarah K. and Jiang، نويسنده , , Guochun and Chandrasekharan، نويسنده , , Mahesh B. and Wilson، نويسنده , , Andrew J. and Zheng، نويسنده , , Siyuan and Yenamandra، نويسنده , , Ashwini and Locke، نويسنده , , Kimberly and Yuan، نويسنده , , Jia-ling and Bonine-Summers، نويسنده , , Alyssa R. and Wells، نويسنده , , Christina E. and Kaiser، نويسنده , , Jonathan F. and Washington، نويسنده , , M. Kay and Zhao، نويسنده , , Zhongming and Wagner، نويسنده , , Florence F. and Sun، نويسنده , , Zu-Wen and Xia، نويسنده , , Fen and Holson، نويسنده , , Edward B. and Khabele، نويسنده , , Dineo and Hiebert، نويسنده , , Scott W.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2010
Pages
12
From page
436
To page
447
Abstract
Summary
is essential for efficient DNA replication and DNA damage control. Deletion of Hdac3 impaired DNA repair and greatly reduced chromatin compaction and heterochromatin content. These defects corresponded to increases in histone H3K9,K14ac; H4K5ac; and H4K12ac in late S phase of the cell cycle, and histone deposition marks were retained in quiescent Hdac3-null cells. Liver-specific deletion of Hdac3 culminated in hepatocellular carcinoma. Whereas HDAC3 expression was downregulated in only a small number of human liver cancers, the mRNA levels of the HDAC3 cofactor NCOR1 were reduced in one-third of these cases. siRNA targeting of NCOR1 and SMRT (NCOR2) increased H4K5ac and caused DNA damage, indicating that the HDAC3/NCOR/SMRT axis is critical for maintaining chromatin structure and genomic stability.
Journal title
Cancer Cell
Serial Year
2010
Journal title
Cancer Cell
Record number
1337284
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