Beuten Joke, Ma Jennie Z, Lou Xiang-Yang, Payne Thomas J, Li Ming D
Department of Psychiatric Medicine, The University of Virginia, Charlottesville, Virginia 22911, USA.
Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):285-90. doi: 10.1002/ajmg.b.30399.
The protein phosphatase 1 regulatory subunit 1B gene (PPP1R1B; also known as dopamine and cAMP-regulated phosphoprotein; DARPP32) is a target for the actions of dopamine. Because the mesolimbic dopaminergic system is implicated in the reinforcing effects of many drugs, including nicotine, PPP1R1B is considered a plausible candidate for involvement in the development of vulnerability to nicotine dependence (ND). Further, this gene is located within a region on chromosome 17 that demonstrated "suggestive linkage" to ND in our previous genome-wide scan. In the present study, we analyzed six single nucleotide polymorphisms (SNPs) within PPP1R1B for association with three ND measures: smoking quantity (SQ), the heaviness of smoking index (HSI), and the Fagerström Test for ND (FTND) score. Our sample consisted of 602 nuclear families of African-American (AA) or European-American (EA) origin. No significant associations were found for single SNPs after correction for multiple testing. However, haplotype analysis indicated that in the EA sample, the C-T-G-C haplotype formed by rs2271309-rs907094-rs3764352-rs3817160 with a frequency of 32.0% was significantly associated with SQ (Z = 2.50; P = 0.01), even after Bonferroni correction. No significant associations with haplotypes were found in the AA sample. In summary, our findings provide the first evidence for the potential involvement of PPP1R1B in the etiology of ND and further investigation is thus warranted.
蛋白磷酸酶1调节亚基1B基因(PPP1R1B;也称为多巴胺和cAMP调节磷蛋白;DARPP32)是多巴胺作用的靶点。由于中脑边缘多巴胺能系统与包括尼古丁在内的许多药物的强化作用有关,因此PPP1R1B被认为是参与尼古丁依赖(ND)易感性发展的一个合理候选基因。此外,该基因位于17号染色体上的一个区域,在我们之前的全基因组扫描中显示与ND存在“提示性连锁”。在本研究中,我们分析了PPP1R1B基因内的六个单核苷酸多态性(SNP)与三种ND指标的关联:吸烟量(SQ)、吸烟强度指数(HSI)和尼古丁依赖的Fagerström测试(FTND)得分。我们的样本由602个非裔美国人(AA)或欧裔美国人(EA)起源的核心家庭组成。在进行多重检验校正后,未发现单个SNP有显著关联。然而,单倍型分析表明,在EA样本中,由rs2271309 - rs907094 - rs3764352 - rs3817160形成的频率为32.0%的C - T - G - C单倍型与SQ显著相关(Z = 2.50;P = 0.01),即使经过Bonferroni校正也是如此。在AA样本中未发现与单倍型有显著关联。总之,我们的研究结果为PPP1R1B可能参与ND的病因学提供了首个证据,因此有必要进行进一步研究。