Mizuno K, Antunes-Martins A, Ris L, Peters M, Godaux E, Giese K P
Wolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK.
Neuroscience. 2007 Mar 16;145(2):393-402. doi: 10.1016/j.neuroscience.2006.11.056. Epub 2007 Jan 3.
The calcium/calmodulin (CaM) kinase cascade regulates gene transcription, which is required for long-term memory formation. Previous studies with Camkk2 null mutant mice have shown that in males calcium/calmodulin kinase kinase beta (CaMKKbeta) is required for spatial memory formation and for activation of the transcription factor cyclic AMP-responsive element binding protein (CREB) in the hippocampus by spatial training. Here we show that CaMKKbeta is not required for spatial memory formation in female mice as female Camkk2 null mutants were not impaired in spatial memory formation and they had the same level of hippocampal CREB phosphorylation after spatial training as female wild-type mice. Furthermore, we show that male but not female Camkk2 null mutants were impaired in long-term potentiation (LTP) at hippocampal CA1 synapses. Finally, a transcriptional analysis of male Camkk2 null mutants led to the identification of a gene, glycosyl phosphatidyl-inositol anchor attachment protein 1 (GAA1), whose hippocampal mRNA expression was up-regulated by spatial and contextual training in male but not in female wild-type mice. Taken together, we conclude that CaMKKbeta has a male-specific function in hippocampal memory formation and we have identified male-restricted transcription occurring during hippocampal memory formation.
钙/钙调蛋白(CaM)激酶级联反应调节基因转录,这是长期记忆形成所必需的。先前对Camkk2基因敲除突变小鼠的研究表明,在雄性小鼠中,钙/钙调蛋白激酶激酶β(CaMKKβ)是空间记忆形成以及通过空间训练激活海马体中转录因子环磷酸腺苷反应元件结合蛋白(CREB)所必需的。在此我们表明,CaMKKβ并非雌性小鼠空间记忆形成所必需的,因为雌性Camkk2基因敲除突变体在空间记忆形成方面并未受损,并且在空间训练后,它们海马体中CREB的磷酸化水平与雌性野生型小鼠相同。此外,我们还表明,雄性而非雌性Camkk2基因敲除突变体在海马体CA1突触的长时程增强(LTP)方面存在缺陷。最后,对雄性Camkk2基因敲除突变体的转录分析导致鉴定出一个基因,即糖基磷脂酰肌醇锚定附着蛋白1(GAA1),在雄性野生型小鼠中,其海马体mRNA表达通过空间和情境训练而上调,而在雌性野生型小鼠中则不然。综上所述,我们得出结论,CaMKKβ在海马体记忆形成中具有雄性特异性功能,并且我们已经鉴定出在海马体记忆形成过程中发生的雄性特异性转录。