Suppr超能文献

SORCS3 及其蛋白相互作用物的独立关联 SNPs 与多种脑相关疾病和特征相关。

Independent Associated SNPs at SORCS3 and Its Protein Interactors for Multiple Brain-Related Disorders and Traits.

机构信息

Department of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad 45320, Pakistan.

Centre for Neuroimaging, Cognition and Genomics (NICOG), School of Biological and Chemical Sciences and School of Psychology, University of Galway, H91 CF50 Galway, Ireland.

出版信息

Genes (Basel). 2023 Feb 14;14(2):482. doi: 10.3390/genes14020482.

Abstract

Sortilin-related vacuolar protein sorting 10 () domain containing receptor 3 () is a neuron-specific transmembrane protein involved in the trafficking of proteins between intracellular vesicles and the plasma membrane. Genetic variation at is associated with multiple neuropsychiatric disorders and behavioural phenotypes. Here, we undertake a systematic search of published genome-wide association studies to identify and catalogue associations between and brain-related disorders and traits. We also generate a gene-set based on protein-protein interactions and investigate the contribution of this gene-set to the heritability of these phenotypes and its overlap with synaptic biology. Analysis of association signals at showed individual SNPs to be associated with multiple neuropsychiatric and neurodevelopmental brain-related disorders and traits that have an impact on the experience of feeling, emotion or mood or cognitive function, while multiple LD-independent SNPs were associated with the same phenotypes. Across these SNPs, alleles associated with the more favourable outcomes for each phenotype (e.g., decreased risk of neuropsychiatric illness) were associated with increased expression of the gene. The gene-set was enriched for heritability contributing to schizophrenia (SCZ), bipolar disorder (BPD), intelligence (IQ) and education attainment (EA). Eleven genes from the gene-set were associated with more than one of these phenotypes at the genome-wide level, with associated with SCZ, IQ and EA. Functional annotation revealed that the gene-set is enriched for multiple ontologies related to the structure and function of synapses. Overall, we find many independent association signals at with brain-related disorders and traits, with the effect possibly mediated by reduced gene expression, resulting in a negative impact on synaptic function.

摘要

Sortilin 相关的液泡分拣蛋白 10 () 结构域包含受体 3 () 是一种神经元特异性跨膜蛋白,参与细胞内囊泡与质膜之间的蛋白质运输。 上的遗传变异与多种神经精神障碍和行为表型有关。 在这里,我们进行了系统的已发表全基因组关联研究搜索,以确定和编目 与脑相关疾病和特征之间的关联。 我们还基于蛋白质-蛋白质相互作用生成了一个 基因集,并研究了该基因集对这些表型的遗传力的贡献及其与突触生物学的重叠。 对 上的关联信号进行分析表明,单个 SNP 与多种神经精神和神经发育性脑相关疾病和特征相关,这些疾病和特征会影响感觉、情绪或情绪或认知功能的体验,而多个 LD 独立的 SNP 与相同的表型相关。 在这些 SNP 中,与每种表型(例如,神经精神疾病风险降低)更有利的结果相关的等位基因与 基因的表达增加相关。 基因集富集了与精神分裂症(SCZ)、双相情感障碍(BPD)、智力(IQ)和教育程度(EA)相关的遗传力。 基因集中的 11 个基因在全基因组水平上与这些表型中的一个以上相关,而 与 SCZ、IQ 和 EA 相关。 功能注释表明, 基因集富集了与突触结构和功能相关的多个本体论。 总体而言,我们在 上发现了许多与脑相关疾病和特征相关的独立关联信号,其作用可能通过降低基因表达来介导,从而对突触功能产生负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f72/9956385/e13470daf9f8/genes-14-00482-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验