Yazdani Neema, Shen Ying, Johnson W Evan, Bryant Camron D
Laboratory of Addiction Genetics, Department of Pharmacology and Experimental Therapeutics and Psychiatry, Boston University School of Medicine, Boston, MA, USA; NIGMS PhD Program in Biomolecular Pharmacology, Department of Pharmacology and Experimental Therapeutics and Psychiatry, Boston University School of Medicine, Boston, MA, USA.
Division of Computational Biomedicine, Boston University School of Medicine, Boston, MA, USA.
Genom Data. 2016 Apr 11;8:77-80. doi: 10.1016/j.gdata.2016.03.009. eCollection 2016 Jun.
Addiction to psychostimulants such as Methamphetamine (MA) is a significant public health issue in the United States and currently, there are no FDA approved pharmacological interventions. Previously, using short term-selected mouse lines for high and low MA sensitivity that were derived from an F2 cross between C57BL/6J (B6) and DBA/2J (D2) strains, we identified a quantitative trait locus (QTL) on chromosome (chr) 11 that influenced sensitivity to MA-induced locomotor activity (D2 < B6). Using interval-specific murine congenic lines containing various D2 allelic segments on a B6 background, we fine mapped the QTL to a 206 kb critical interval on chromosome 11. To investigate the neurobiological mechanism by which this QTL decreases MA sensitivity, we conducted transcriptome analysis in a 10 Mb congenic mouse (chromosome 11: 50-60 Mb) on whole-striatum brain tissue punches compared to wild-type B6 littermate controls [1]. The data from this study can be found in the NCBI Gene Expression Omnibus (GSE66366).
对甲基苯丙胺(MA)等精神兴奋剂上瘾是美国一个重大的公共卫生问题,目前尚无美国食品药品监督管理局(FDA)批准的药物干预措施。此前,我们利用从C57BL/6J(B6)和DBA/2J(D2)品系之间的F2杂交中获得的对MA敏感性高和低的短期选择小鼠品系,在11号染色体(chr)上鉴定出一个影响对MA诱导的运动活动敏感性的数量性状基因座(QTL)(D2 < B6)。利用在B6背景上包含各种D2等位基因片段的区间特异性小鼠近交系,我们将该QTL精细定位到11号染色体上一个206 kb的关键区间。为了研究该QTL降低MA敏感性的神经生物学机制,我们对全纹状体脑组织切片进行了转录组分析,使用的是一只10 Mb近交小鼠(11号染色体:50 - 60 Mb),并与野生型B6同窝对照进行比较[1]。这项研究的数据可在NCBI基因表达综合数据库(GSE66366)中找到。