Regulation of neuronal traits by a novel transcriptional complex

被引:357
作者
Ballas, N
Battaglioli, E
Atouf, F
Andres, ME
Chenoweth, J
Anderson, ME
Burger, C
Moniwa, M
Davie, JR
Bowers, WJ
Federoff, HJ
Rose, DW
Rosenfeld, MG
Brehm, P
Mandel, G [1 ]
机构
[1] SUNY Stony Brook, Howard Hughes Med Inst, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Dept Neurobiol & Behav, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
[4] Manitoba Inst Cell Biol, Winnipeg, MB R3E 0V9, Canada
[5] Univ Calif San Diego, Div Endocrinol & Metab, La Jolla, CA 92093 USA
[6] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
[7] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[8] Univ Rochester, Sch Med, Dept Neurol, Rochester, NY 14642 USA
[9] Univ Rochester, Sch Med, Ctr Aging & Dev Biol, Rochester, NY 14642 USA
关键词
D O I
10.1016/S0896-6273(01)00371-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The transcriptional repressor, REST, helps restrict neuronal traits to neurons by blocking their expression In nonneuronal cells. To examine the repercussions of REST expression in neurons, we generated a neuronal cell line that expresses REST conditionally. REST expression inhibited differentiation by nerve growth factor, suppressing both sodium current and neurite growth. A novel corepressor complex, CoREST/HDAC2, was shown to be required for REST repression. In the presence of REST, the CoREST/HDAC2 complex occupied the native Nav1.2 sodium channel gene In chromatin. In neuronal cells that lack REST and express sodium channels, the corepressor complex was not present on the gene. Collectively, these studies define a novel HDAC complex that is recruited by the C-terminal repressor domain of REST to actively repress genes essential to the neuronal phenotype.
引用
收藏
页码:353 / 365
页数:13
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