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PPP3CC 基因与双相情感障碍的关联,该基因编码钙调神经磷酸酶 γ 催化亚基。

Association between the PPP3CC gene, coding for the calcineurin gamma catalytic subunit, and bipolar disorder.

机构信息

INSERM U-513, Faculté de Médecine, 8 rue de Général Sarrail, 94000, Créteil, France.

出版信息

Behav Brain Funct. 2008 Jan 17;4:2. doi: 10.1186/1744-9081-4-2.

Abstract

BACKGROUND

Calcineurin is a neuron-enriched phosphatase that regulates synaptic plasticity and neuronal adaptation. Activation of calcineurin, overall, antagonizes the effects of the cyclic AMP activated protein/kinase A. Thus, kinase/phosphatase dynamic balance seems to be critical for transition to long-term cellular responses in neurons, and disruption of this equilibrium should induce behavioral impairments in animal models. Genetic animal models, as well as post-mortem studies in humans have implicated calcineurin dependent calcium and cyclic AMP regulated phosphorylation/dephosphorylation in both affective responses and psychosis. Recently, genetic association between schizophrenia and genetic variation of the human calcineurin A gamma subunit gene (PPP3CC) has been reported.

METHODS

Based on the assumption of the common underlying genetic factor in schizophrenia and bipolar affective disorder (BPAD), we performed association analysis of CC33 and CCS3 polymorphisms of the PPP3CC gene reported to be associated with schizophrenia in a French sample of 115 BPAD patients and 97 healthy controls.

RESULTS

Carrying 'CT' or 'TT' genotypes of the PPP3CC-CC33 polymorphism increased risk to develop BPAD comparing to carry 'CC' genotype (OR = 1.8 [1.01-3.0]; p = 0.05). For the PPP3CC-CCS3 polymorphism, 'AG' or 'GG' carriers have an increased risk to develop BPAD than 'AA' carriers (OR = 2.8 [1.5-5.2]). The CC33 and CCS3 polymorphisms were observed in significant linkage disequilibrium (D' = 0.91, r2 = 0.72). Haplotype frequencies were significantly different in BPAD patients than in controls (p = 0.03), with a significant over-transmission of the 'TG' haplotype in BPAD patients (p = 0.001).

CONCLUSION

We suggest that the PPP3CC gene might be a susceptibility gene for BPAD, in accordance with current neurobiological hypotheses that implicate dysregulation of signal-transduction pathways, such as those regulated by calcineurin, in the etiology of affective disorders.

摘要

背景

钙调神经磷酸酶是一种富含神经元的磷酸酶,可调节突触可塑性和神经元适应。钙调神经磷酸酶的激活总体上拮抗环 AMP 激活的蛋白/激酶 A 的作用。因此,激酶/磷酸酶的动态平衡似乎对神经元中向长期细胞反应的转变至关重要,而这种平衡的破坏应该会在动物模型中引起行为障碍。遗传动物模型以及人类的死后研究表明,钙调神经磷酸酶依赖性钙和环 AMP 调节的磷酸化/去磷酸化在情感反应和精神病中都有牵连。最近,有人报道了精神分裂症和人类钙调神经磷酸酶 A γ亚基基因(PPP3CC)的遗传变异之间的遗传关联。

方法

基于精神分裂症和双相情感障碍(BPAD)之间存在共同潜在遗传因素的假设,我们对已报道与法国 115 例 BPAD 患者和 97 名健康对照者的精神分裂症相关的 PPP3CC 基因的 CC33 和 CCS3 多态性进行了关联分析。

结果

与携带“CC”基因型相比,PPP3CC-CC33 多态性的“CT”或“TT”基因型携带者发生 BPAD 的风险增加(OR=1.8[1.01-3.0];p=0.05)。对于 PPP3CC-CCS3 多态性,“AG”或“GG”携带者发生 BPAD 的风险高于“AA”携带者(OR=2.8[1.5-5.2])。CC33 和 CCS3 多态性之间存在显著的连锁不平衡(D'=0.91,r2=0.72)。BPAD 患者的单倍型频率与对照组显著不同(p=0.03),BPAD 患者的“TG”单倍型明显过度传递(p=0.001)。

结论

我们认为 PPP3CC 基因可能是 BPAD 的易感基因,这与当前的神经生物学假设一致,即涉及钙调神经磷酸酶等信号转导途径的失调在情感障碍的发病机制中起作用。

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