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Gem相互作用蛋白(GMIP)基因与重度抑郁症有关。

The Gem interacting protein (GMIP) gene is associated with major depressive disorder.

作者信息

Tadokoro Kazuyuki, Hashimoto Ryota, Tatsumi Masahiko, Kosuga Asako, Kamijima Kunitoshi, Kunugi Hiroshi

机构信息

Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, 187-8502, Japan.

出版信息

Neurogenetics. 2005 Sep;6(3):127-33. doi: 10.1007/s10048-005-0003-3. Epub 2005 Sep 28.

Abstract

Major depressive disorder (MDD) is a mood disorder with a significant heritable component. Structural neuronal impairment has been considered to be implicated in MDD, as it leads to brain morphological alterations such as hippocampal atrophy. The Gem interacting protein, GMIP, is a novel Rho GTPase-activating protein known to play important roles in neurite growth and axonal guidance. We examined the GMIP gene for possible association in a Japanese sample of 164 patients with MDD and 164 controls matched for sex. We found a significant association with MDD for one single nucleotide polymorphism (SNP) (-525G/A) located on the 5'-upstream region of the GMIP gene (p=0.039, odds ratio 1.66, 95% CI 1.05-2.69) and stronger evidence for association in a multimarker haplotype analysis (p=0.004). We then performed a promoter-luciferase reporter assay; the promoter activity for -525A allele, which was in excess in the MDD patients, was significantly decreased compared with the -525G allele in transient transfection experiments using three types of cell lines. Our results suggest that genetic variations in the GMIP gene can confer susceptibility to MDD, and the associated promoter SNP might play a role in the transcriptional regulation of the GMIP gene. Further study needs to be undertaken to validate the association between the GMIP gene and MDD.

摘要

重度抑郁症(MDD)是一种具有显著遗传成分的情绪障碍。结构性神经元损伤被认为与MDD有关,因为它会导致大脑形态改变,如海马萎缩。Gem相互作用蛋白GMIP是一种新型的Rho GTP酶激活蛋白,已知在神经突生长和轴突导向中起重要作用。我们在164例MDD患者和164例性别匹配的对照组成的日本样本中检测了GMIP基因的可能关联。我们发现GMIP基因5'上游区域的一个单核苷酸多态性(SNP)(-525G/A)与MDD有显著关联(p = 0.039,优势比1.66,95%可信区间1.05 - 2.69),并且在多标记单倍型分析中有更强的关联证据(p = 0.004)。然后我们进行了启动子 - 荧光素酶报告基因检测;在使用三种细胞系的瞬时转染实验中,MDD患者中过量的 -525A等位基因的启动子活性与 -525G等位基因相比显著降低。我们的结果表明,GMIP基因的遗传变异可能导致对MDD的易感性,并且相关的启动子SNP可能在GMIP基因的转录调控中起作用。需要进一步研究来验证GMIP基因与MDD之间的关联。

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