Sequential increase in Egr-1 and AP-1 DNA binding activity in the dentate gyrus following the induction of long-term potentiation

被引:32
作者
Williams, JM [1 ]
Beckmann, AM
Mason-Parker, SE
Abraham, WC
Wilce, PA
Tate, WP
机构
[1] Univ Otago, Dept Biochem, Dunedin, New Zealand
[2] Univ Otago, Ctr Gene Res, Dunedin, New Zealand
[3] Univ Queensland, Dept Biochem, Alcohol Res Unit, St Lucia, Qld, Australia
[4] Univ Otago, Dept Psychol, Dunedin, New Zealand
[5] Univ Otago, Neurosci Res Ctr, Dunedin, New Zealand
来源
MOLECULAR BRAIN RESEARCH | 2000年 / 77卷 / 02期
基金
英国医学研究理事会;
关键词
transcription factor; gel shift assay; long-term potentiation;
D O I
10.1016/S0169-328X(00)00061-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Establishment of long-term potentiation (LTP) at perforant path synapses is highly correlated with increased expression of Egr and AP-1 transcription factors in rat dentate gyrus granule cells. We have investigated whether increased transcription factor levels are reflected in increased transcription factor activity by assessing Egr and AP-I DNA binding activity using gel shift assays. LTP produced an increase in binding to the Egr element, which was NMDA receptor-dependent and correlated closely with our previously reported increase in Egr-1 (zif/268) protein levels. Supershift analysis confirmed involvement of Egr-1, but not Egr-2 in the DNA binding activity. AP-1 DNA binding was also rapidly elevated in parallel with protein levels, however, the peak increase in activity was delayed until 4 h, a time point when we have previously shown that only jun-D protein was elevated. These data indicate that binding of Egr-1 and AP-1 to their response elements is increased in two phases. This may result in activation of distinct banks of target genes which contribute to the establishment of persistent LTP. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:258 / 266
页数:9
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