Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.
Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Transl Psychiatry. 2017 Aug 22;7(8):e1212. doi: 10.1038/tp.2017.183.
Understanding molecular processes that link comorbid traits such as addictions and mental disorders can provide novel therapeutic targets. Neuregulin signaling pathway (NSP) has previously been implicated in schizophrenia, a neurodevelopmental disorder with high comorbidity to smoking. Using a Finnish twin family sample, we have previously detected association between nicotine dependence and ERBB4 (a neuregulin receptor), and linkage for smoking initiation at the ERBB4 locus on 2q33. Further, Neuregulin3 has recently been shown to associate with nicotine withdrawal in a behavioral mouse model. In this study, we scrutinized association and linkage between 15 036 common, low frequency and rare genetic variants in 10 NSP genes and phenotypes encompassing smoking and alcohol use. Using the Finnish twin family sample (N=1998 from 740 families), we detected 66 variants (representing 23 LD blocks) significantly associated (false discovery rate P<0.05) with smoking initiation, nicotine dependence and nicotine withdrawal. We comprehensively annotated the associated variants using expression (eQTL) and methylation quantitative trait loci (meQTL) analyses in a Finnish population sample. Among the 66 variants, we identified 25 eQTLs (in NRG1 and ERBB4), 22 meQTLs (in NRG3, ERBB4 and PSENEN), a missense variant in NRG1 (rs113317778) and a splicing disruption variant in ERBB4 (rs13385826). Majority of the QTLs in blood were replicated in silico using publicly available databases, with additional QTLs observed in brain. In conclusion, our results support the involvement of NSP in smoking behavior but not in alcohol use and abuse, and disclose functional potential for 56 of the 66 associated single-nucleotide polymorphism.
理解将成瘾和精神障碍等共病特征联系起来的分子过程可以提供新的治疗靶点。神经调节素信号通路(NSP)先前与精神分裂症有关,精神分裂症是一种具有高吸烟共病性的神经发育障碍。使用芬兰双胞胎家庭样本,我们先前在尼古丁依赖和 ERBB4(神经调节素受体)之间检测到关联,并且在 2q33 上的 ERBB4 基因座上检测到吸烟起始的连锁。此外,最近在行为小鼠模型中表明神经调节素 3 与尼古丁戒断有关。在这项研究中,我们仔细研究了 10 个 NSP 基因和包含吸烟和饮酒的表型中 15036 个常见、低频和稀有遗传变异之间的关联和连锁。使用芬兰双胞胎家庭样本(来自 740 个家庭的 1998 名个体),我们检测到 66 个变体(代表 23 个 LD 块)与吸烟起始、尼古丁依赖和尼古丁戒断显著相关(错误发现率 P<0.05)。我们使用芬兰人群样本中的表达(eQTL)和甲基化数量性状基因座(meQTL)分析全面注释相关变体。在 66 个变体中,我们鉴定了 25 个 eQTL(在 NRG1 和 ERBB4 中)、22 个 meQTL(在 NRG3、ERBB4 和 PSENEN 中)、NRG1 中的错义变体(rs113317778)和 ERBB4 中的剪接破坏变体(rs13385826)。血液中的大多数 QTL 可以使用公开可用的数据库在计算机上进行复制,并且在大脑中观察到额外的 QTL。总之,我们的结果支持 NSP 参与吸烟行为,但不参与饮酒和滥用行为,并揭示了 66 个相关单核苷酸多态性中的 56 个的功能潜力。