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P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder

机译:P2RX7是编码嘌呤能配体门控离子通道的基因,与重度抑郁症有关

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摘要

The P2RX7 gene is located within a region on chromosome 12q24.31 that has been identified as a susceptibility locus for affective disorders by linkage and association studies. P2RX7 is a purinergic ATP-binding calcium channel expressed in neurons as well as in microglial cells in various brain regions. We investigated 29 single nucleotide polymorphisms (SNPs) within the P2RX7 gene and adjacent genes in a sample of 1000 German Caucasian patients suffering from recurrent major depressive disorder (MDD). These were contrasted with diagnosed healthy Caucasian controls from the same population (n=1029). A non-synonymous coding SNP in the P2RX7 gene (rs2230912), previously found to be associated with bipolar disorder, was significantly associated (P=0.0019) with MDD. This polymorphism results in an amino acid exchange in the C-terminal cytosolic domain of the P2RX7 channel protein, suggesting that the observed P2RX7 polymorphism might play a causal role in the development of depression.
机译:P2RX7基因位于染色体12q24.31上的一个区域内,该区域已通过连锁和关联研究确定为情感障碍的易感基因座。 P2RX7是在神经元以及大脑各个区域的小神经胶质细胞中表达的嘌呤能ATP结合钙通道。我们在1000名患有复发性重性抑郁症(MDD)的德国高加索患者样本中调查了P2RX7基因和邻近基因中的29个单核苷酸多态性(SNP)。这些与来自同一人群(n = 1029)的经诊断的健康白种人对照形成对照。先前发现与双相情感障碍有关的P2RX7基因(rs2230912)中的非同义编码SNP与MDD显着相关(P = 0.0019)。这种多态性导致P2RX7通道蛋白的C末端胞质域中的氨基酸交换,这表明观察到的P2RX7多态性可能在抑郁症的发生中起因果作用。

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