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首页> 外文期刊>Neurochemical Research >Mapping of QTLs for Oral Alcohol Self-Administration in B6.C and B6.I Quasi-Congenic RQI Strains
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Mapping of QTLs for Oral Alcohol Self-Administration in B6.C and B6.I Quasi-Congenic RQI Strains

机译:B6.C和B6.I准同类RQI菌株中口服酒精自我管理的QTL定位

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摘要

One strategy to identify neurochemical pathways of addiction is to map the relevant genes. In the present study we used 43 B6.C and 35 B6.I inbred RQI mouse strains, carrying <3% donor genome on C57BL/6ByJ background, for gene mapping. The strains were phenotyped for consumption of alcohol (12% v/v) in a two-bottle-choice paradigm, and genotyped for 396 microsatellite markers. The current mapping study extends our earlier experiment scanning five mouse chromosomes (Vadasz et al. (2000) Scanning of five chromosomes for alcohol consumption loci. Alcohol 22:25–34) to a whole-genome study, and discusses the differences and limitations. Data were analyzed with composite interval (CIM) and multiple interval (MIM) QTL mapping methods. CIM of B6.C strains detected significant QTLs on chrs. 6 and 12. A suggestive, but not significant, locus was detected in the B6.I strains on chr. 12. The best MIM model for B6.C strains confirmed one QTL on chr. 6 and one QTL on chr. 12, while the MIM model for the B6.I strains confirmed the suggestive locus on chr. 12. Some of the QTLs for alcohol consumption are new, while others confirm previously reported QTLs for alcohol preference, and alcohol acceptance.
机译:识别成瘾的神经化学途径的一种策略是定位相关基因。在本研究中,我们使用了43个B6.C和35个B6.I自交系RQI小鼠品系,它们在C57BL / 6ByJ背景上携带<3%的供体基因组,用于基因定位。在两瓶选择范式中对菌株进行表型分析以测定其酒精消耗量(12%v / v),并对396个微卫星标记进行基因分型。当前的作图研究将我们先前的扫描五个小鼠染色体的实验(Vadasz等人(2000年),对酒精消耗基因座的五个染色体的扫描。酒精22:25-34)扩展到了全基因组研究,并讨论了其区别和局限性。使用复合间隔(CIM)和多间隔(MIM)QTL映射方法分析数据。 B6.C菌株的CIM在chrs上检测到明显的QTL。参见图6和12。在hr的B6.I菌株中检测到提示性的但不显着的基因座。 12. B6.C菌株的最佳MIM模型证实了chr的一个QTL。 6和一个Chr QTL。如图12所示,而针对B6.I菌株的MIM模型证实了chr上的提示基因座。 12.一些用于饮酒的QTL是新的,而其他一些则确认先前报告的关于酒精偏好和接受酒精的QTL。

著录项

  • 来源
    《Neurochemical Research》 |2007年第7期|1099-1112|共14页
  • 作者单位

    Laboratory of Neurobehavioral Genetics Nathan S. Kline Institute for Psychiatric Research 140 Old Orangeburg Road Orangeburg NY 10962 USA;

    Laboratory of Neurobehavioral Genetics Nathan S. Kline Institute for Psychiatric Research 140 Old Orangeburg Road Orangeburg NY 10962 USA;

    Laboratory of Neurobehavioral Genetics Nathan S. Kline Institute for Psychiatric Research 140 Old Orangeburg Road Orangeburg NY 10962 USA;

    Laboratory of Neurobehavioral Genetics Nathan S. Kline Institute for Psychiatric Research 140 Old Orangeburg Road Orangeburg NY 10962 USA;

    Laboratory of Neurobehavioral Genetics Nathan S. Kline Institute for Psychiatric Research 140 Old Orangeburg Road Orangeburg NY 10962 USA;

    Laboratory of Neurobehavioral Genetics Nathan S. Kline Institute for Psychiatric Research 140 Old Orangeburg Road Orangeburg NY 10962 USA;

    Laboratory of Neurobehavioral Genetics Nathan S. Kline Institute for Psychiatric Research 140 Old Orangeburg Road Orangeburg NY 10962 USA;

    Diabetes Research Centre Western Australian Institute for Medical Research Level 6 50 Murray St Perth WA 6000 Australia;

    Laboratory of Neurobehavioral Genetics Nathan S. Kline Institute for Psychiatric Research 140 Old Orangeburg Road Orangeburg NY 10962 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    QTL mapping; Quasi-congenic mouse; Recombinant QTL introgression; Ethanol consumption; Addiction;

    机译:QTL定位;拟同类小鼠;重组QTL基因渗入;乙醇消耗;成瘾;

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