McClintick Jeanette N, Brooks Andrew I, Deng Li, Liang Li, Wang Jen C, Kapoor Manav, Xuei Xiaoling, Foroud Tatiana, Tischfield Jay A, Edenberg Howard J
Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA.
Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers University, Piscataway, NJ, USA.
Alcohol. 2014 Sep;48(6):603-10. doi: 10.1016/j.alcohol.2014.07.004. Epub 2014 Jul 22.
To elucidate the effects of a controlled exposure to ethanol on gene expression, we studied lymphoblastoid cell lines (LCLs) from 21 alcoholics and 21 controls. We cultured each cell line for 24 h with and without 75 mM ethanol and measured gene expression using microarrays. Differences in expression between LCLs from alcoholics and controls included 13 genes previously identified as associated with alcoholism or related traits, including KCNA3, DICER1, ZNF415, CAT, SLC9A9, and PPARGC1B. The paired design allowed us to detect very small changes due to ethanol treatment: ethanol altered the expression of 37% of the probe sets (51% of the unique named genes) expressed in these LCLs, most by modest amounts. Ninety-nine percent of the named genes expressed in the LCLs were also expressed in brain. Key pathways affected by ethanol include cytokine, TNF, and NFκB signaling. Among the genes affected by ethanol were ANK3, EPHB1, SLC1A1, SLC9A9, NRD1, and SH3BP5, which were reported to be associated with alcoholism or related phenotypes in 2 genome-wide association studies. Genes that either differed in expression between alcoholics and controls or were affected by ethanol exposure are candidates for further study.
为了阐明乙醇的可控暴露对基因表达的影响,我们研究了来自21名酗酒者和21名对照者的淋巴母细胞系(LCLs)。我们将每个细胞系在含有和不含有75 mM乙醇的条件下培养24小时,并使用微阵列测量基因表达。酗酒者和对照者的LCLs之间的表达差异包括13个先前被确定与酗酒或相关特征相关的基因,包括KCNA3、DICER1、ZNF415、CAT、SLC9A9和PPARGC1B。配对设计使我们能够检测到由于乙醇处理引起的非常小的变化:乙醇改变了这些LCLs中37%的探针集(51%的独特命名基因)的表达,大多数变化量适中。在LCLs中表达的99%的命名基因在大脑中也有表达。受乙醇影响的关键途径包括细胞因子、TNF和NFκB信号传导。在受乙醇影响的基因中,ANK3、EPHB1、SLC1A1、SLC9A9、NRD1和SH3BP5在两项全基因组关联研究中被报道与酗酒或相关表型有关。在酗酒者和对照者之间表达不同或受乙醇暴露影响的基因是进一步研究的候选对象。