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酒精偏好和非偏好大鼠中α-突触核蛋白表达的调控

Regulation of alpha-synuclein expression in alcohol-preferring and -non preferring rats.

作者信息

Liang Tiebing, Carr Lucinda G

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis, 46202, USA.

出版信息

J Neurochem. 2006 Oct;99(2):470-82. doi: 10.1111/j.1471-4159.2006.04111.x.

Abstract

The alpha-synuclein (Snca) gene is expressed at higher levels in alcohol-naïve, inbred alcohol-preferring (iP) rats than in alcohol-non preferring (iNP) rats. Snca modulates dopamine transmission and the dopamineregic system, which play a role in mediating the rewarding properties of alcohol consumption. Thus, understanding regulation of Snca gene expression could provide insight into the relationship of Snca and alcohol consumption. To study regulation of rat Snca expression, 1,912 bp of the iP and iNP 5'-regions were cloned and sequenced. 5'-rapid amplification of cDNA ends (RACE), primer extension and RT-PCR mapped three transcription start site clusters (clusters TSS1, TSS2 and TSS3), suggesting that the Snca proximal promoter region has a complex architecture. This proximal promoter region has three TATA-less core promoters containing SP1 binding sites, initiator elements and downstream core promoter elements, which are often located in such promoters. Snca-luc constructs transiently transfected into SK-N-SH neuroblastoma cells showed that the region from - 1,912 to - 1,746 contained a strong core promoter, and that the entire approximately 2 kb region had significant promoter activity. Five polymorphisms identified between the iP and iNP in the proximal promoter region did not influence differential expression between the strains. In contrast, a single nucleotide polymorphism (SNP) at + 679 in the 3'-untranslated region (UTR) resulted in a 1.3-fold longer half-life of iP mRNA compared with iNP mRNA, which is consistent with the differential expression observed between the iP and iNP strains. These results suggest that regulation of rat Snca gene expression is complex and may contribute to alcohol preference in the iP rats.

摘要

α-突触核蛋白(Snca)基因在未接触酒精的近交系嗜酒(iP)大鼠中的表达水平高于非嗜酒(iNP)大鼠。Snca调节多巴胺传递和多巴胺能系统,这在介导酒精摄入的奖赏特性中发挥作用。因此,了解Snca基因表达的调控机制有助于深入了解Snca与酒精摄入之间的关系。为了研究大鼠Snca表达的调控,克隆并测序了iP和iNP 5'区域的1912 bp。5'-cDNA末端快速扩增(RACE)、引物延伸和RT-PCR确定了三个转录起始位点簇(TSS1、TSS2和TSS3簇),表明Snca近端启动子区域具有复杂的结构。该近端启动子区域有三个无TATA的核心启动子,包含SP1结合位点、起始子元件和下游核心启动子元件,这些元件常位于此类启动子中。瞬时转染到SK-N-SH神经母细胞瘤细胞中的Snca-luc构建体显示,-1912至-1746区域包含一个强核心启动子,整个约2 kb区域具有显著的启动子活性。在近端启动子区域的iP和iNP之间鉴定出的五个多态性不影响品系间的差异表达。相比之下,3'非翻译区(UTR)中+679处的一个单核苷酸多态性(SNP)导致iP mRNA的半衰期比iNP mRNA长1.3倍,这与在iP和iNP品系间观察到的差异表达一致。这些结果表明,大鼠Snca基因表达的调控是复杂 的,可能导致iP大鼠对酒精的偏好。

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