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

机译:编码钙调神经磷酸酶γ催化亚基的PPP3CC基因与躁郁症之间的关联

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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.
机译: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性。钙调神经磷酸酶的活化总体上拮抗环状AMP活化的蛋白/激酶A的作用。因此,激酶/磷酸酶的动态平衡似乎对于过渡到神经元中的长期细胞反应至关重要,并且这种平衡的破坏应引起行为障碍在动物模型中。遗传动物模型以及在人体中进行的事后研究均表明,钙调神经磷酸酶依赖性钙和环AMP调节的磷酸化/去磷酸化作用在情感反应和精神病方面均涉及。最近,已经报道了精神分裂症与人钙调神经磷酸酶Aγ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)共同的潜在遗传因素的假设,我们对法国115例BPAD患者和97例BP97CC患者中据报道与精神分裂症相关的PPP3CC基因的CC33和CCS3多态性进行了关联分析。健康对照。结果与携带“ CC”基因型的人相比,携带PPP3CC-CC33多态性的“ CT”或“ TT”基因型的人患BPAD的风险增加(OR = 1.8 [1.01-3.0]; p = 0.05)。对于PPP3CC-CCS3多态性,与“ AA”携带者相比,“ AG”或“ GG”携带者患BPAD的风险增加(OR = 2.8 [1.5-5.2])。在明显的连锁不平衡中观察到CC33和CCS3多态性(D'= 0.91,r 2 = 0.72)。 BPAD患者的单倍型频率与对照组显着不同(p = 0.03),BPAD患者的'TG'单倍型显着超传(p = 0.001)。结论:根据目前的神经生物学假说,我们认为PPP3CC基因可能是BPAD的易感基因,这种假说暗示了情感障碍病因中信号转导途径的异常调节,例如钙调神经磷酸酶所调节的那些。

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