单核苷酸多态性
生物
遗传学
嘌呤能受体
基因座(遗传学)
重性抑郁障碍
基因
SNP公司
编码区
等位基因
人口
基因型
受体
内分泌学
医学
环境卫生
扁桃形结构
作者
Susanne Lucae,Daria Salyakina,Nicholas Barden,Mario Harvey,Bernard Gagné,Michel Labbé,Elisabeth B. Binder,Manfred Uhr,Marcelo Páez-Pereda,Inge Sillaber,Marcus Ising,Tanja Brückl,Roselind Lieb,Herta Flor,Bertram Müller-Myhsok
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI