Individual histone deacetylases in Drosophila modulate transcription of distinct genes

被引:56
作者
Cho, YS [1 ]
Griswold, A [1 ]
Campbell, C [1 ]
Min, KT [1 ]
机构
[1] NINDS, Neurogenet Branch, NIH, Bethesda, MD 20892 USA
关键词
drosophila; HDACs; microarray; aging; HDAC inhibitors;
D O I
10.1016/j.ygeno.2005.07.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Lysine residues on the N-terminal tails of histories in chromatin are the primary targets of histone acetyltransferases (HATs) and histone deacetylases (HDACs) in eukaryotes. Regulation of historic acetylation by these two classes of enzymes plays significant roles in controlling transcriptional activity in cells. Eukaryotic organisms have several different HDACs, but the biological roles of each HDAC are still not clear. To understand the physiological functions of HDACs, we characterized six different Drosophila HDACs, including Rpd3, HDAC3, HDAC4, HDAC6-S, HDAC6-L, and Sir2, by developmental expression pattern, transcriptional profiles of target genes, and sensitivity to HDAC inhibitors. We found that each HDAC has a distinct temporal expression pattern and regulates transcription of a unique set of genes. Furthermore, we demonstrated differential sensitivity of HDACs to inhibitors. These results show that each individual HDAC plays different roles in regulating genes involved in various biological processes. Published by Elsevier Inc.
引用
收藏
页码:606 / 617
页数:12
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