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Brain Behav. 2018 Mar 22;8(5):e00961. doi: 10.1002/brb3.961. eCollection 2018 May.
2
Pronounced strain-specific chemosensory receptor gene expression in the mouse vomeronasal organ.在小鼠犁鼻器中表达明显的菌株特异性化学感觉受体基因。
BMC Genomics. 2017 Dec 12;18(1):965. doi: 10.1186/s12864-017-4364-4.
3
Intravenously Infused F3.Olig2 Improves Memory Deficits via Restoring Myelination in the Aged Hippocampus Following Experimental Ischemic Stroke.静脉注射F3.Olig2通过恢复实验性缺血性中风后老年海马体的髓鞘形成来改善记忆缺陷。
Cell Transplant. 2016 Dec 13;25(12):2129-2144. doi: 10.3727/096368916X692230. Epub 2016 Jul 20.
4
Oligodendrocyte and Interneuron Density in Hippocampal Subfields in Schizophrenia and Association of Oligodendrocyte Number with Cognitive Deficits.精神分裂症海马亚区少突胶质细胞和中间神经元密度以及少突胶质细胞数量与认知缺陷的关联
Front Cell Neurosci. 2016 Mar 30;10:78. doi: 10.3389/fncel.2016.00078. eCollection 2016.
5
ASSOCIATION STUDY BETWEEN OLIGODENDROCYTE TRANSCRIPTION FACTOR 2 GENE AND OBSESSIVE-COMPULSIVE DISORDER IN A CHINESE HAN POPULATION.中文人群少突胶质转录因子 2 基因与强迫症的关联研究。
Depress Anxiety. 2015 Oct;32(10):720-7. doi: 10.1002/da.22394. Epub 2015 Aug 14.
6
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Pharmacogenet Genomics. 2015 May;25(5):239-45. doi: 10.1097/FPC.0000000000000129.
7
A meta-analysis of gene expression quantitative trait loci in brain.大脑中基因表达数量性状位点的荟萃分析。
Transl Psychiatry. 2014 Oct 7;4(10):e459. doi: 10.1038/tp.2014.96.
8
Genetic variability in the regulation of gene expression in ten regions of the human brain.人类大脑十个区域中基因表达调控的遗传变异性。
Nat Neurosci. 2014 Oct;17(10):1418-1428. doi: 10.1038/nn.3801. Epub 2014 Aug 31.
9
Oligodendrocyte-encoded HIF function couples postnatal myelination and white matter angiogenesis.少突胶质细胞编码的 HIF 功能将出生后髓鞘形成和白质血管生成偶联。
Cell. 2014 Jul 17;158(2):383-396. doi: 10.1016/j.cell.2014.04.052. Epub 2014 Jul 10.
10
Crosstalk between cerebral endothelium and oligodendrocyte.脑内皮细胞与少突胶质细胞的串扰。
Cell Mol Life Sci. 2014 Mar;71(6):1055-66. doi: 10.1007/s00018-013-1488-9. Epub 2013 Oct 17.

种族依赖性:OLIG2 基因精神分裂症风险变异对 OLIG2 转录和白质完整性的影响。

Ethnicity-Dependent Effects of Schizophrenia Risk Variants of the OLIG2 Gene on OLIG2 Transcription and White Matter Integrity.

机构信息

Department of Psychiatry, Miyagi Psychiatric Center, Natori, Japan.

Department of Disaster Psychiatry, Graduate School of Medicine, Tohoku University, Sendai, Japan.

出版信息

Schizophr Bull. 2020 Dec 1;46(6):1619-1628. doi: 10.1093/schbul/sbaa049.

DOI:10.1093/schbul/sbaa049
PMID:32285113
原文链接:
https://pmc.ncbi.nlm.nih.gov/articles/PMC7846078/
Abstract

Previous studies have indicated associations between several OLIG2 gene single-nucleotide polymorphisms (SNPs) and susceptibility to schizophrenia among Caucasians. Consistent with these findings, postmortem brain and diffusion tensor imaging studies have indicated that the schizophrenia-risk-associated allele (A) in the OLIG2 SNP rs1059004 predicts lower OLIG2 gene expression in the dorsolateral prefrontal cortex (DLPFC) of schizophrenia patients and reduced white matter (WM) integrity of the corona radiata in normal brains among Caucasians. In an effort to replicate the association between this variant and WM integrity among healthy Japanese, we found that the number of A alleles was positively correlated with WM integrity in some fiber tracts, including the right posterior limb of the internal capsule, and with mean blood flow in a widespread area, including the inferior frontal operculum, orbital area, and triangular gyrus. Because the A allele affected WM integrity in opposite directions in Japanese and Caucasians, we investigated a possible association between the OLIG2 gene SNPs and the expression level of OLIG2 transcripts in postmortem DLPFCs. We evaluated rs1059004 and additional SNPs in the 5' upstream and 3' downstream regions of rs1059004 to cover the broader region of the OLIG2 gene. The 2 SNPs (rs1059004 and rs9653711) had opposite effects on OLIG2 gene expression in the DLPFC in Japanese and Caucasians. These findings suggest ethnicity-dependent opposite effects of OLIG2 gene SNPs on WM integrity and OLIG2 gene expression in the brain, which may partially explain the failures in replicating associations between genetic variants and psychiatric phenotypes among ethnicities.

摘要

先前的研究表明,几个 OLIG2 基因单核苷酸多态性(SNP)与白种人精神分裂症易感性之间存在关联。与这些发现一致的是,尸检大脑和弥散张量成像研究表明,OLIG2 SNP rs1059004 中与精神分裂症风险相关的等位基因(A)预测精神分裂症患者背外侧前额叶皮质(DLPFC)中的 OLIG2 基因表达降低,以及白种人正常大脑中放射冠的白质(WM)完整性降低。为了在健康的日本人群中复制该变体与 WM 完整性之间的关联,我们发现 A 等位基因的数量与某些纤维束的 WM 完整性呈正相关,包括右侧内囊后肢,以及包括额下回、眶额区和三角脑回在内的广泛区域的平均血流。由于 A 等位基因在日本人和白种人中对 WM 完整性的影响方向相反,我们研究了 OLIG2 基因 SNP 与尸检 DLPFC 中 OLIG2 转录本表达水平之间的可能关联。我们评估了 rs1059004 和 rs1059004 5'上游和 3'下游区域的其他 SNPs,以涵盖 OLIG2 基因的更广泛区域。这 2 个 SNP(rs1059004 和 rs9653711)对日本人和白种人 DLPFC 中的 OLIG2 基因表达具有相反的影响。这些发现表明,OLIG2 基因 SNP 对 WM 完整性和大脑中 OLIG2 基因表达的影响具有种族依赖性的相反作用,这可能部分解释了在不同种族中遗传变异与精神表型之间的关联复制失败的原因。