Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona, Barcelona, Catalonia, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
Sci Rep. 2017 Aug 31;7(1):10110. doi: 10.1038/s41598-017-10207-2.
Genetic factors involved in the susceptibility to drug addiction still remain largely unknown. MiRNAs seem to play key roles in the drug-induced plasticity of the brain that likely drives the emergence of addiction. In this work we explored the role of miRNAs in drug addiction. With this aim, we selected 62 SNPs located in the 3'UTR of target genes that are predicted to alter the binding of miRNA molecules and performed a case-control association study in a Spanish sample of 735 cases (mainly cocaine-dependent subjects with multiple drug dependencies) and 739 controls. We found an association between rs1047383 in the PLCB1 gene and drug dependence that was replicated in an independent sample (663 cases and 667 controls). Then we selected 9 miRNAs predicted to bind the rs1047383 region, but none of them showed any effect on PLCB1 expression. We also assessed two miRNAs binding a region that contains a SNP in linkage disequilibrium with rs1047383, but although one of them, hsa-miR-582, was found to downregulate PLCB1, no differences were observed between alleles. Finally, we explored the possibility that PLCB1 expression is altered by cocaine and we observed a significant upregulation of the gene in the nucleus accumbens of cocaine abusers and in human dopaminergic-like neurons after cocaine treatment. Our results, together with previous studies, suggest that PLCB1 participates in the susceptibility to drug dependence.
遗传因素在药物成瘾易感性中的作用仍知之甚少。miRNAs 似乎在药物引起的大脑可塑性中发挥关键作用,这可能导致成瘾的出现。在这项工作中,我们探讨了 miRNAs 在药物成瘾中的作用。为此,我们选择了位于靶基因 3'UTR 中的 62 个 SNP,这些 SNP 预测会改变 miRNA 分子的结合,然后在一个西班牙样本中进行了病例对照关联研究,该样本包括 735 例病例(主要是可卡因依赖者,有多种药物依赖)和 739 例对照。我们发现 PLCB1 基因中的 rs1047383 与药物依赖之间存在关联,在独立样本中得到了复制(663 例病例和 667 例对照)。然后,我们选择了 9 个被预测与 rs1047383 区域结合的 miRNA,但没有一个对 PLCB1 表达有影响。我们还评估了两个与 rs1047383 连锁不平衡的 SNP 区域结合的 miRNA,但尽管其中一个,hsa-miR-582,被发现下调 PLCB1,但等位基因之间没有观察到差异。最后,我们探讨了 cocaine 是否改变 PLCB1 表达的可能性,结果发现可卡因滥用者的伏隔核中该基因显著上调,可卡因处理后人多巴胺样神经元中该基因也显著上调。我们的结果与以前的研究一起表明,PLCB1 参与了药物依赖的易感性。