Ramagopalan Sreeram V, Maugeri Narelle J, Handunnetthi Lahiru, Lincoln Matthew R, Orton Sarah-Michelle, Dyment David A, Deluca Gabriele C, Herrera Blanca M, Chao Michael J, Sadovnick A Dessa, Ebers George C, Knight Julian C
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
PLoS Genet. 2009 Feb;5(2):e1000369. doi: 10.1371/journal.pgen.1000369. Epub 2009 Feb 6.
Multiple sclerosis (MS) is a complex trait in which allelic variation in the MHC class II region exerts the single strongest effect on genetic risk. Epidemiological data in MS provide strong evidence that environmental factors act at a population level to influence the unusual geographical distribution of this disease. Growing evidence implicates sunlight or vitamin D as a key environmental factor in aetiology. We hypothesised that this environmental candidate might interact with inherited factors and sought responsive regulatory elements in the MHC class II region. Sequence analysis localised a single MHC vitamin D response element (VDRE) to the promoter region of HLA-DRB1. Sequencing of this promoter in greater than 1,000 chromosomes from HLA-DRB1 homozygotes showed absolute conservation of this putative VDRE on HLA-DRB115 haplotypes. In contrast, there was striking variation among non-MS-associated haplotypes. Electrophoretic mobility shift assays showed specific recruitment of vitamin D receptor to the VDRE in the HLA-DRB115 promoter, confirmed by chromatin immunoprecipitation experiments using lymphoblastoid cells homozygous for HLA-DRB115. Transient transfection using a luciferase reporter assay showed a functional role for this VDRE. B cells transiently transfected with the HLA-DRB115 gene promoter showed increased expression on stimulation with 1,25-dihydroxyvitamin D3 (P = 0.002) that was lost both on deletion of the VDRE or with the homologous "VDRE" sequence found in non-MS-associated HLA-DRB1 haplotypes. Flow cytometric analysis showed a specific increase in the cell surface expression of HLA-DRB1 upon addition of vitamin D only in HLA-DRB1*15 bearing lymphoblastoid cells. This study further implicates vitamin D as a strong environmental candidate in MS by demonstrating direct functional interaction with the major locus determining genetic susceptibility. These findings support a connection between the main epidemiological and genetic features of this disease with major practical implications for studies of disease mechanism and prevention.
多发性硬化症(MS)是一种复杂的性状,其中MHC II类区域的等位基因变异对遗传风险产生最强的单一影响。MS的流行病学数据提供了强有力的证据,表明环境因素在人群水平上起作用,影响这种疾病异常的地理分布。越来越多的证据表明阳光或维生素D是病因中的关键环境因素。我们假设这种环境候选因素可能与遗传因素相互作用,并在MHC II类区域寻找反应性调控元件。序列分析将单个MHC维生素D反应元件(VDRE)定位到HLA-DRB1的启动子区域。对来自HLA-DRB1纯合子的1000多条染色体上的该启动子进行测序,结果显示在HLA-DRB115单倍型上该假定的VDRE绝对保守。相比之下,非MS相关单倍型之间存在显著差异。电泳迁移率变动分析显示维生素D受体特异性募集到HLA-DRB115启动子中的VDRE,这通过使用HLA-DRB115纯合的淋巴母细胞进行的染色质免疫沉淀实验得到证实。使用荧光素酶报告基因测定法进行的瞬时转染显示该VDRE具有功能作用。用HLA-DRB115基因启动子瞬时转染的B细胞在1,25-二羟基维生素D3刺激下表达增加(P = 0.002),在缺失VDRE或在非MS相关的HLA-DRB1单倍型中发现的同源“VDRE”序列时这种增加消失。流式细胞术分析显示仅在携带HLA-DRB1*15的淋巴母细胞中添加维生素D后HLA-DRB1的细胞表面表达特异性增加。这项研究通过证明与决定遗传易感性的主要基因座直接功能相互作用,进一步表明维生素D是MS中一个强有力的环境候选因素。这些发现支持了这种疾病的主要流行病学和遗传特征之间的联系,对疾病机制和预防研究具有重要的实际意义。