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Single Nucleotide Polymorphisms in the 3′UTR of VPAC-1 Cooperate in Modulating Gene Expression and Impact Differently on the Interaction with miR525-5p

机译:VPAC-1的3UTR中的单核苷酸多态性合作调节基因表达和对miR525-5p相互作用的不同影响。

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摘要

Complex immune and neurodegenerative disorders are the result of multiple interactions between common genetic variations having, individually, a weak effect on the disease susceptibility or resistance. Interestingly, some genes have been found to be associated with more than one disease although not necessarily the same SNPs are involved. In this context, single nucleotide polymorphisms in the 3′UTR region of type 1 receptor (VPAC-1) for vasoactive intestinal peptide (VIP) have been reported to be associated with some immune-mediated as well as with neurodegenerative diseases such as Alzheimer's Disease (AD). Here, we demonstrate that variations at the 3′UTR of the VPAC-1 gene act synergistically to affect the expression of the luciferase as well as of the GFP reporter genes expressed in HEK293T cells. Moreover, the miRNA 525-5p, previously shown by us to target the 3′UTR of VPAC-1, is more efficient in decreasing GFP expression when co-expressed with constructs carrying the allele C at rs896 (p<10-3) suggesting that this miRNA regulates VPAC-1 expression at different levels depending on rs896 polymorphism and thus adding complexity to the network of disease susceptibility.
机译:复杂的免疫和神经退行性疾病是常见遗传变异之间多次相互作用的结果,这些变异对疾病的易感性或耐药性影响较弱。有趣的是,尽管不一定涉及相同的SNP,但已经发现一些基因与一种以上的疾病有关。在这种情况下,据报道血管活性肠肽(VIP)的1型受体3'UTR区(VPAC-1)的单核苷酸多态性与某些免疫介导的疾病以及神经退行性疾病(例如阿尔茨海默氏病)有关(广告)。在这里,我们证明了VPAC-1基因3'UTR处的变异具有协同作用,以影响荧光素酶以及HEK293T细胞中表达的GFP报告基因的表达。此外,我们先前展示的靶向VPAC-1的3'UTR的miRNA 525-5p在与在rs896上携带等位基因C的构建体共表达时,在降低GFP表达方面更有效(p <10 <- 3 )提示该miRNA根据rs896多态性在不同水平上调节VPAC-1的表达,从而增加了疾病易感性网络的复杂性。

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