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Regulation of hippocampus‐dependent memory by the zinc finger protein Zbtb20 in mature CA1 neurons
Author(s) -
Ren Anjing,
Zhang Huan,
Xie Zhifang,
Ma Xianhua,
Ji Wenli,
He David Z.Z.,
Yuan Wenjun,
Ding YuQiang,
Zhang XiaoHui,
Zhang Weiping J.
Publication year - 2012
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2012.234187
Subject(s) - long term potentiation , neuroscience , creb , hippocampus , excitatory postsynaptic potential , hippocampal formation , nmda receptor , biology , mapk/erk pathway , neuronal memory allocation , microbiology and biotechnology , phosphorylation , transcription factor , receptor , inhibitory postsynaptic potential , synaptic fatigue , biochemistry , gene
Key points• Zinc finger and BTB domain‐containing protein 20 (Zbtb20) plays a critical role in hippocampal development. • In the present study, we generated mutant mice in which Zbtb20 knockout was restricted to mature CA1 pyramidal cells of the hippocampus. • Conditionally deleting Zbtb20 specifically in mature CA1 pyramidal neurons impaired LTP and memory. • We found that Zbtb20 controls memory formation and synaptic plasticity by regulating NMDAR activity, and activation of ERK and CREB.Abstract The mammalian hippocampus harbours neural circuitry that is crucial for associative learning and memory. The mechanisms that underlie the development and regulation of this complex circuitry are not fully understood. Our previous study established an essential role for the zinc finger protein Zbtb20 in the specification of CA1 field identity in the developing hippocampus. Here, we show that conditionally deleting Zbtb20 specifically in mature CA1 pyramidal neurons impaired hippocampus‐dependent memory formation, without affecting hippocampal architecture or the survival, identity and basal excitatory synaptic activity of CA1 pyramidal neurons. We demonstrate that mature CA1‐specific Zbtb20 knockout mice exhibited reductions in long‐term potentiation (LTP) and NMDA receptor (NMDAR)‐mediated excitatory post‐synaptic currents. Furthermore, we show that activity‐induced phosphorylation of ERK and CREB is impaired in the hippocampal CA1 of Zbtb20 mutant mice. Collectively, these results indicate that Zbtb20 in mature CA1 plays an important role in LTP and memory by regulating NMDAR activity, and activation of ERK and CREB.