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本文引用的文献

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Gene expression within the extended amygdala of 5 pairs of rat lines selectively bred for high or low ethanol consumption.在 5 对选择性繁殖的高或低乙醇消耗大鼠品系的延伸杏仁核内的基因表达。
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Whole brain and brain regional coexpression network interactions associated with predisposition to alcohol consumption.与饮酒倾向相关的全脑和脑区共表达网络相互作用。
PLoS One. 2013 Jul 23;8(7):e68878. doi: 10.1371/journal.pone.0068878. Print 2013.
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Microarray-assisted pathway analysis identifies MT1X & NFκB as mediators of TCRP1-associated resistance to cisplatin in oral squamous cell carcinoma.微阵列辅助途径分析确定 MT1X 和 NFκB 为 TCRP1 相关顺铂耐药性在口腔鳞状细胞癌中的介质。
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Chemosensory responsiveness to ethanol and its individual sensory components in alcohol-preferring, alcohol-nonpreferring and genetically heterogeneous rats.酒精偏爱、非酒精偏爱和遗传异质大鼠对乙醇及其各个感官成分的化学感觉反应。
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Pharmacologically relevant intake during chronic, free-choice drinking rhythms in selectively bred high alcohol-preferring mice.在选择性繁殖的高酒精偏好小鼠的慢性、自由选择饮酒节律中,药物相关的摄入。
Addict Biol. 2013 Nov;18(6):921-9. doi: 10.1111/j.1369-1600.2011.00412.x. Epub 2011 Nov 29.
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Mouse genomic variation and its effect on phenotypes and gene regulation.小鼠基因组变异及其对表型和基因调控的影响。
Nature. 2011 Sep 14;477(7364):289-94. doi: 10.1038/nature10413.
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TCRP1 promotes radioresistance of oral squamous cell carcinoma cells via Akt signal pathway.TCRP1 通过 Akt 信号通路促进口腔鳞状细胞癌细胞的放射抵抗性。
Mol Cell Biochem. 2011 Nov;357(1-2):107-13. doi: 10.1007/s11010-011-0880-8. Epub 2011 May 21.
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A systems genetic analysis of alcohol drinking by mice, rats and men: influence of brain GABAergic transmission.小鼠、大鼠和人类饮酒行为的系统遗传学分析:脑 GABA 能传递的影响。
Neuropharmacology. 2011 Jun;60(7-8):1269-80. doi: 10.1016/j.neuropharm.2010.12.019. Epub 2010 Dec 23.
10
Fine mapping quantitative trait loci that influence alcohol preference behavior in the High and Low Alcohol Preferring (HAP and LAP) mice.精细定位影响高和低酒精偏好(HAP 和 LAP)小鼠酒精偏好行为的数量性状基因座。
Behav Genet. 2011 Jul;41(4):565-70. doi: 10.1007/s10519-010-9414-5. Epub 2010 Dec 24.

基因表达的遗传学特征表明了对酒精偏好选择性育种的反应。

Genetics of gene expression characterizes response to selective breeding for alcohol preference.

作者信息

Hoffman P L, Saba L M, Flink S, Grahame N J, Kechris K, Tabakoff B

机构信息

Department of Pharmacology, University of Colorado School of Medicine, Aurora, CO.

出版信息

Genes Brain Behav. 2014 Nov;13(8):743-57. doi: 10.1111/gbb.12175. Epub 2014 Sep 29.

DOI:10.1111/gbb.12175
PMID:25160899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4241152/
Abstract

Numerous selective breeding experiments have been performed with rodents, in an attempt to understand the genetic basis for innate differences in preference for alcohol consumption. Quantitative trait locus (QTL) analysis has been used to determine regions of the genome that are associated with the behavioral difference in alcohol preference/consumption. Recent work suggests that differences in gene expression represent a major genetic basis for complex traits. Therefore, the QTLs are likely to harbor regulatory regions (eQTLs) for the differentially expressed genes that are associated with the trait. In this study, we examined brain gene expression differences over generations of selection of the third replicate lines of high and low alcohol-preferring (HAP3 and LAP3) mice, and determined regions of the genome that control the expression of these differentially expressed genes (de eQTLs). We also determined eQTL regions (rv eQTLs) for genes that showed a decrease in variance of expression levels over the course of selection. We postulated that de eQTLs that overlap with rv eQTLs, and also with phenotypic QTLs, represent genomic regions that are affected by the process of selection. These overlapping regions controlled the expression of candidate genes (that displayed differential expression and reduced variance of expression) for the predisposition to differences in alcohol consumption by the HAP3/LAP3 mice.

摘要

为了理解对酒精消费偏好的先天差异的遗传基础,人们对啮齿动物进行了大量选择性育种实验。数量性状基因座(QTL)分析已被用于确定基因组中与酒精偏好/消费行为差异相关的区域。最近的研究表明,基因表达差异是复杂性状的主要遗传基础。因此,QTL可能包含与该性状相关的差异表达基因的调控区域(eQTL)。在本研究中,我们检查了高酒精偏好(HAP3)和低酒精偏好(LAP3)小鼠第三代重复品系在多代选择过程中的脑基因表达差异,并确定了控制这些差异表达基因(de eQTL)表达的基因组区域。我们还确定了在选择过程中表达水平方差降低的基因的eQTL区域(rv eQTL)。我们推测,与rv eQTL以及表型QTL重叠的de eQTL代表了受选择过程影响的基因组区域。这些重叠区域控制了HAP3/LAP3小鼠酒精消费差异易感性的候选基因(显示差异表达和表达方差降低)的表达。