Regulatory signal transduction pathways for class IIa histone deacetylases

被引:121
作者
Parra, Maribel [2 ]
Verdin, Eric [1 ,3 ]
机构
[1] Gladstone Inst Virol & Immunol, San Francisco, CA 94158 USA
[2] Bellvitge Biomed Res Inst IDIBELL, Cellular Differentiat Grp, Canc Epigenet & Biol Program PEBC, Barcelona 08907, Spain
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
关键词
PROTEIN-KINASE-D; CARDIAC-HYPERTROPHY; NUCLEAR EXPORT; MYOSIN PHOSPHATASE; SKELETAL-MUSCLE; PHOSPHORYLATION; EXPRESSION; HDAC7; PROTEIN-KINASE-D1; TRANSCRIPTION;
D O I
10.1016/j.coph.2010.04.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The class IIa histone deacetylases (HDACs), HDAC4, 5, 7, and 9, have crucial roles in the development of the immune system and other organs, including brain, heart, and muscle. In addition to their catalytic domain, they are characterized by a large amino-terminal extension. The amino-terminal domain is subject to reversible phosphorylation, which controls their nucleo-cytoplasmic distribution. Unphosphorylated, class IIa HDACs remain in the nucleus, bound to chromatin, and repress transcription. Upon phosphorylation, they shuttle out of the nucleus, allowing derepression of their target genes. Thus, the nucleo-cytoplasmic translocation is associated with derepression of target genes. Recent studies identified the kinases and phosphatases that regulate the nucleocytoplasmic shuttling of class IIa HDACs. Here we will summarize this rapidly evolving field with a particular focus on the immune system.
引用
收藏
页码:454 / 460
页数:7
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