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Identification of a Nuclear Respiratory Factor 1 Recognition Motif in the Apolipoprotein E Variant APOE4 linked to Alzheimer’s Disease

机译:与阿尔茨海默病联系的载脂蛋白E变体APOE4中核呼吸因子1识别基序的鉴定

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Alzheimer’s disease affects tens of millions of people worldwide and its prevalence continues to rise. It is caused by a combination of a subject’s heredity, environment, lifestyle, and medical condition. The most significant genetic risk factor for late onset Alzheimer’s disease is a variant of the apolipoprotein E gene, APOE4. Here we show that the single nucleotide polymorphism rs429358 that defines APOE4 is located in a short sequence motif repeated several times within exon 4 of apolipoprotein E, reminiscent of the structure of transcriptional enhancers. A JASPAR database search predicts that the T to C transition in rs429358 generates a binding motif for nuclear respiratory factor NRF1. This site appears to be part of a binding site cluster for this transcription factor on exon 4 of APOE. This de novo NRF1 binding site has therefore the potential to affect the expression of multiple genes in its genomic vicinity. Our in silico analysis, suggesting a novel function for APOE4 at the DNA level, offers a potential mechanism for the observed tissue specific neurodegeneration and the role of environmental factors in Alzheimer’s disease etiology.
机译:阿尔茨海默病的疾病影响了全球数百万的人,其普遍存在继续上升。它是由受试者的遗传,环境,生活方式和医疗状况的组合引起的。最初发作的阿尔茨海默病的最显着的遗传危险因素是载脂蛋白E基因,ApoE4的变体。在这里,我们表明,定义apoE4的单个核苷酸多态性RS429358位于载脂蛋白E的外显子4内重复几次,使转录增强剂的结构复杂多次。 JASPAR数据库搜索预测RS429358中的T至C转换产生核呼吸系统因子NRF1的结合图案。该站点似乎是Apoe的外显子4上该转录因子的绑定站点集群的一部分。因此,该de Novo NRF1结合位点因此有可能影响其基因组附近的多种基因的表达。我们在Silico分析中,表明DNA水平的APOE4的新功能,为观察到的组织特异性神经变性和环境因素在阿尔茨海默病病因中的作用提供了潜在的机制。

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