Department of Molecular Genetics and Biology of Complex Diseases, Institute of Medical Research A Lanari-IDIM, University of Buenos Aires-National Council of Scientific and Technological Research (CONICET), Ciudad Autónoma de Buenos Aires, Argentina.
Chronobiol Int. 2010 Jul;27(6):1202-18. doi: 10.3109/07420528.2010.496913.
Serotonergic neurotransmission and the master circadian CLOCK gene are physiological modulators of the circadian system. In addition, both are involved in the physiopathology of metabolic syndrome (MS). The authors sought to examine the potential effect of the gene-gene interaction between the functional 44-bp insertion/deletion polymorphism in the promoter region (serotonin-transporter-linked promoter region polymorphism or 5-HTTLPR) of the serotonin transporter gene (SLC6A4) and common variants of the gene CLOCK on the genetic risk underlying MS of shift-workers. To test this hypothesis, 856 men were studied; 518 dayworkers were compared with 338 rotating shiftworkers. Medical history, health examination including anthropometric and arterial blood pressure measurements, a questionnaire on health-related behaviors, and biochemical determinations were obtained from every participant. 5-HTTLPR genotypes were determined using polymerase chain reaction followed by gel electrophoresis. Six tag single-nucleotide polymorphisms (SNPs) in the CLOCK gene with a minor allele frequency >10 % (rs1554483 C/G, rs11932595 A/G, rs4580704 C/G, rs6843722 A/C, rs6850524 C/G, and rs4864548 A/G), encompassing 117 kb of chromosome 4 and representing 115 polymorphic sites (r(2) > .8), were genotyped. A significant interaction between the 5-HTTLPR variant and the haplotype rs1554483-rs4864548 of the CLOCK gene was detected for diastolic (p = .0058) and systolic blood pressure (p = .0014), arterial hypertension (p = .033), plasma triglycerides levels (p = .033), and number of MS components (p = .01). In all these cases, the higher values were observed in rotating shiftworkers homozygous for the SLC6A4 S allele and carrying the haplotype composed by the CLOCK rs1554483 G and rs4864548 A variants. In conclusion, these data suggest a potential interaction (epistatic effect) of serotonin transporter and CLOCK gene variation on the genetic susceptibility to develop MS by rotating shiftworkers.
5-羟色胺能神经传递和主生物钟基因(CLOCK)是生物钟系统的生理调节剂。此外,两者都与代谢综合征(MS)的病理生理学有关。作者试图研究 5-羟色胺转运体基因(SLC6A4)启动子区域的功能性 44-bp 插入/缺失多态性(5-羟色胺转运体相关启动子区域多态性或 5-HTTLPR)与基因 CLOCK 的常见变异之间的基因-基因相互作用对轮班工人 MS 的遗传风险的潜在影响。为了检验这一假设,研究了 856 名男性;将 518 名白班工人与 338 名轮班工人进行了比较。每位参与者都接受了医学史、健康检查,包括人体测量和动脉血压测量、健康相关行为问卷以及生化测定。使用聚合酶链反应(PCR)后凝胶电泳法确定 5-HTTLPR 基因型。CLOCK 基因中有 6 个标记单核苷酸多态性(SNP),其等位基因频率>10%(rs1554483C/G、rs11932595A/G、rs4580704C/G、rs6843722A/C、rs6850524C/G 和 rs4864548A/G),涵盖染色体 4 的 117kb,代表 115 个多态性位点(r(2)>0.8),进行了基因分型。检测到 5-HTTLPR 变体与 CLOCK 基因的 rs1554483-rs4864548 单倍型之间存在显著的相互作用,用于舒张压(p=0.0058)和收缩压(p=0.0014)、高血压(p=0.033)、血浆甘油三酯水平(p=0.033)和 MS 成分数(p=0.01)。在所有这些情况下,在 SLC6A4 S 等位基因纯合且携带由 CLOCK rs1554483 G 和 rs4864548 A 变体组成的单倍型的轮班工人中观察到更高的值。总之,这些数据表明 5-羟色胺转运体和 CLOCK 基因变异之间存在潜在的相互作用(上位效应),可能导致轮班工人易患 MS。