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α-Synuclein maps to a quantitative trait locus for alcohol preference and is differentially expressed in alcohol-preferring and -nonpreferring rats

机译:α-突触核蛋白映射到酒精偏好的定量性状基因座,并且在偏好酒精和不偏好酒精的大鼠中差异表达

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摘要

Total gene expression analysis (TOGA) was used to identify genes that are differentially expressed in brain regions between the alcohol-naïve, inbred alcohol-preferring (iP), and -nonpreferring (iNP) rats. α-Synuclein, expressed at >2-fold higher levels in the hippocampus of the iP than the iNP rat, was prioritized for further study. In situ hybridization was used to determine specific brain regions and cells expressing α-synuclein in the iP and iNP rats. Similar to α-synuclein mRNA levels, protein levels in the hippocampus were higher in iP rats than iNP rats. Higher protein levels were also observed in the caudate putamen of iP rats compared with iNP rats. Sequence analysis identified two single nucleotide polymorphisms in the 3′ UTR of the cDNA. The polymorphism was used to map the gene, by using recombination-based methods, to chromosome 4, within a quantitative trait locus for alcohol consumption that was identified in the iP and iNP rats. A nucleotide exchange in the iNP 3′ UTR reduced expression of the luciferase reporter gene in SK-N-SH neuroblastoma cells. These results suggest that differential expression of the α-synuclein gene may contribute to alcohol preference in the iP rats.
机译:总基因表达分析(TOGA)用于鉴定在未饮酒,近交嗜酒精(iP)和非嗜酒(iNP)大鼠之间脑区差异表达的基因。优先研究iP海马中i-Synuclein的表达水平高于iNP大鼠2倍。原位杂交用于确定iP和iNP大鼠中特定的大脑区域和表达α-突触核蛋白的细胞。与α-突触核蛋白mRNA水平相似,iP大鼠的海马蛋白水平高于iNP大鼠。与iNP大鼠相比,iP大鼠的尾状壳中也观察到更高的蛋白质水平。序列分析确定了cDNA 3'UTR中的两个单核苷酸多态性。通过使用基于重组的方法,将多态性用于将基因定位到4号染色体上的iP和iNP大鼠中确定的酒精消耗的定量性状基因座。 iNP 3'UTR中的核苷酸交换降低了SK-N-SH神经母细胞瘤细胞中荧光素酶报道基因的表达。这些结果表明,α-突触核蛋白基因的差异表达可能有助于iP大鼠的酒精嗜好。

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