Dumas Laura, Dickens C Michael, Anderson Nathan, Davis Jonathan, Bennett Beth, Radcliffe Richard A, Sikela James M
Department of Biochemistry and Molecular Genetics, University of Colorado Denver School of Medicine, Aurora, CO, 80045, USA,
Mamm Genome. 2014 Jun;25(5-6):235-43. doi: 10.1007/s00335-014-9502-6. Epub 2014 Feb 20.
It has been well documented that genetic factors can influence predisposition to develop alcoholism. While the underlying genomic changes may be of several types, two of the most common and disease associated are copy number variations (CNVs) and sequence alterations of protein coding regions. The goal of this study was to identify CNVs and single-nucleotide polymorphisms that occur in gene coding regions that may play a role in influencing the risk of an individual developing alcoholism. Toward this end, two mouse strains were used that have been selectively bred based on their differential sensitivity to alcohol: the Inbred long sleep (ILS) and Inbred short sleep (ISS) mouse strains. Differences in initial response to alcohol have been linked to risk for alcoholism, and the ILS/ISS strains are used to investigate the genetics of initial sensitivity to alcohol. Array comparative genomic hybridization (arrayCGH) and exome sequencing were conducted to identify CNVs and gene coding sequence differences, respectively, between ILS and ISS mice. Mouse arrayCGH was performed using catalog Agilent 1 × 244 k mouse arrays. Subsequently, exome sequencing was carried out using an Illumina HiSeq 2000 instrument. ArrayCGH detected 74 CNVs that were strain-specific (38 ILS/36 ISS), including several ISS-specific deletions that contained genes implicated in brain function and neurotransmitter release. Among several interesting coding variations detected by exome sequencing was the gain of a premature stop codon in the alpha-amylase 2B (AMY2B) gene specifically in the ILS strain. In total, exome sequencing detected 2,597 and 1,768 strain-specific exonic gene variants in the ILS and ISS mice, respectively. This study represents the most comprehensive and detailed genomic comparison of ILS and ISS mouse strains to date. The two complementary genome-wide approaches identified strain-specific CNVs and gene coding sequence variations that should provide strong candidates to contribute to the alcohol-related phenotypic differences associated with these strains.
有充分的文献记载表明,遗传因素会影响患酒精中毒症的易感性。虽然潜在的基因组变化可能有几种类型,但最常见且与疾病相关的两种是拷贝数变异(CNV)和蛋白质编码区域的序列改变。本研究的目的是识别基因编码区域中可能影响个体患酒精中毒症风险的CNV和单核苷酸多态性。为此,使用了两种基于对酒精的不同敏感性而进行选择性培育的小鼠品系:近交长睡眠(ILS)小鼠品系和近交短睡眠(ISS)小鼠品系。对酒精的初始反应差异与患酒精中毒症的风险有关,ILS/ISS品系用于研究对酒精初始敏感性的遗传学。分别进行了阵列比较基因组杂交(arrayCGH)和外显子组测序,以识别ILS和ISS小鼠之间的CNV和基因编码序列差异。使用安捷伦1×244k小鼠目录阵列进行小鼠arrayCGH。随后,使用Illumina HiSeq 2000仪器进行外显子组测序。arrayCGH检测到74个品系特异性的CNV(38个ILS/36个ISS),包括几个ISS特异性缺失,这些缺失包含与脑功能和神经递质释放相关的基因。在外显子组测序检测到的几个有趣的编码变异中,α-淀粉酶2B(AMY2B)基因中出现了一个提前终止密码子的增加,且该情况仅在ILS品系中出现。外显子组测序总共在ILS和ISS小鼠中分别检测到2597个和1768个品系特异性的外显子基因变异。这项研究是迄今为止对ILS和ISS小鼠品系最全面、最详细的基因组比较。这两种互补的全基因组方法识别出品系特异性的CNV和基因编码序列变异,这些变异应该能为导致与这些品系相关的酒精相关表型差异提供有力的候选因素。