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γ-氨基丁酸Aα6基因5'侧翼区域的五个突变与突变的撒丁岛非嗜酒大鼠中基础的和乙醇诱导的α6上调减少有关。

Five mutations in the GABA A alpha6 gene 5' flanking region are associated with a reduced basal and ethanol-induced alpha6 upregulation in mutated Sardinian alcohol non-preferring rats.

作者信息

Saba Luisella, Porcella Anna, Sanna Angela, Congeddu Elena, Marziliano Nicola, Mongeau Raymond, Grayson Dennis, Pani Luca

机构信息

Neuroscienze Pharmaness S.C.aR.L, Cagliari, Italy.

出版信息

Brain Res Mol Brain Res. 2005 Jun 13;137(1-2):252-7. doi: 10.1016/j.molbrainres.2004.07.024. Epub 2005 Apr 18.

DOI:10.1016/j.molbrainres.2004.07.024
PMID:15950783
Abstract

The presence of four nucleotide changes and a three base-pair deletion in the GABA A alpha6-subunit promoter is described in Sardinian alcohol non-preferring rats, selectively bred for their ethanol aversion. These mutations are associated with the R100Q alpha6 intragenic mutation that was previously characterized in the same animals. The possibility that these mutated nucleotides alter the ethanol-induced upregulation of the alpha6 gene was investigated by measuring cerebellar alpha6 mRNA levels after a chronic ethanol liquid diet in sNP rat. Real-time quantitative PCR showed an increased alpha6 gene expression after ethanol ingestion in normal and mutated rats. However, lower amounts of alpha6 mRNA levels were detected both in control and in ethanol-treated sNP rats carrying the five promoter and the intragenic mutations in a homozygous state. Using the electromobility shift assay, specific DNA binding sites were found in cerebellar extracts of the alpha6 regions comprising the five mutations. These results suggest that one or more of the mutated binding sites that were found in the 5' flanking alpha6 region may be a consensus sequence for regulatory factors which are responsible for both basal and ethanol-induced alpha6 gene expression.

摘要

在撒丁岛酒精不偏好大鼠中描述了GABAAα6亚基启动子中四个核苷酸变化和一个三碱基对缺失的情况,这些大鼠是因其对乙醇的厌恶而被选择性培育的。这些突变与先前在同一动物中鉴定出的R100Qα6基因内突变相关。通过测量慢性乙醇液体饮食后sNP大鼠小脑α6 mRNA水平,研究了这些突变核苷酸是否改变乙醇诱导的α6基因上调。实时定量PCR显示,正常和突变大鼠摄入乙醇后α6基因表达增加。然而,在纯合状态下携带五个启动子和基因内突变的对照和乙醇处理的sNP大鼠中,均检测到较低水平的α6 mRNA。使用电泳迁移率变动分析,在包含五个突变的α6区域的小脑提取物中发现了特异性DNA结合位点。这些结果表明,在5'侧翼α6区域发现的一个或多个突变结合位点可能是负责基础和乙醇诱导的α6基因表达的调节因子的共有序列。

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