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zif268基因表达的遗传与活性依赖性调控:与空间学习的关联

Genetic and activity-dependent regulation of zif268 expression: association with spatial learning.

作者信息

Fordyce D E, Bhat R V, Baraban J M, Wehner J M

机构信息

Institute for Behavioral Genetics, University of Colorado, Boulder 80309-0477.

出版信息

Hippocampus. 1994 Oct;4(5):559-68. doi: 10.1002/hipo.450040505.

Abstract

We have reported that C57BL/6 and DBA/2 mice differ in spatial learning performance and associated hippocampal protein kinase C (PKC) activity (Upchurch and Wehner, 1989, Behav Neurosci 103:1251-1258; Wehner et al., 1990, Brain Res 523:181-187) and that physical activity enhances spatial learning with related alterations in protein kinase C (PKC) (Fordyce and Wehner, 1993b, Brain Res 619:111-119). To assess whether physical activity induces alterations in gene expression that may underlie these changes in PKC and learning performance, we examined the effect of physical activity on expression of zif268, a transcription regulatory factor linked to stimulus-induced neuronal plasticity. C57 and DBA mice, 3 months of age, were subjected to acute (one bout) or chronic (8 weeks) physical activity. The mice were then tested on the Morris water maze task for 6 days with subsequent analysis of PKC activity and zif268 mRNA expression. Control DBA mice, which have poor hippocampal-specific learning performance compared to C57 mice (Wehner et al., 1990, Brain Res 523-181-187; Fordyce and Wehner, 1993b, Brain Res 619:111-119; Paylor et al., 1993, Psychobiology 27:11-26), displayed lower basal levels of zif268 mRNA (P < .05). As observed previously, chronic physical activity produced an enhancement in spatial learning performance accompanied by alterations in hippocampal PKC activity in both strains of mice (P < .05). In addition, the present investigation demonstrated that acute physical activity increased mRNA levels of zif268 in hippocampal regions CA1, CA3 and overlying cortex (P < .005) of both C57 and DBA mice. Chronic physical activity suppressed the basal expression of zif268 in C57 mice in CA1 and overlying cortex below control levels. These findings suggest that genetic and activity-dependent regulation of zif268 may influence learning performance.

摘要

我们曾报道,C57BL/6和DBA/2小鼠在空间学习能力以及相关的海马蛋白激酶C(PKC)活性方面存在差异(Upchurch和Wehner,1989年,《行为神经科学》103:1251 - 1258;Wehner等人,1990年,《脑研究》523:181 - 187),并且体力活动可通过蛋白激酶C(PKC)的相关改变来增强空间学习能力(Fordyce和Wehner,1993b年,《脑研究》619:111 - 119)。为了评估体力活动是否会诱导基因表达的改变,而这种改变可能是PKC和学习能力变化的基础,我们研究了体力活动对zif268表达的影响,zif268是一种与刺激诱导的神经元可塑性相关的转录调节因子。对3月龄的C57和DBA小鼠进行急性(单次)或慢性(8周)体力活动。然后让小鼠在莫里斯水迷宫任务中测试6天,随后分析PKC活性和zif268 mRNA表达。与C57小鼠相比,对照DBA小鼠的海马特异性学习能力较差(Wehner等人,1990年,《脑研究》523 - 181 - 187;Fordyce和Wehner,1993b年,《脑研究》619:111 - 119;Paylor等人,1993年,《心理生物学》27:11 - 26),其zif268 mRNA的基础水平较低(P < .05)。如先前观察到的,慢性体力活动使两种品系小鼠的空间学习能力增强,同时海马PKC活性发生改变(P < .05)。此外,本研究表明,急性体力活动使C57和DBA小鼠海马CA1区、CA3区及覆盖皮层的zif268 mRNA水平升高(P < .005)。慢性体力活动使C57小鼠CA1区及覆盖皮层的zif268基础表达低于对照水平。这些发现表明,zif268的基因和活动依赖性调节可能会影响学习能力。

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