Pricop L, Li L, Salmon J E, Jacob C O
Department of Medicine, Hospital for Special Surgery and Weill Medical College of Cornell University New York, NY 10021, USA.
Genes Immun. 2002 Oct;3 Suppl 1:S47-50. doi: 10.1038/sj.gene.6363873.
FcgammaRIIA is a candidate gene involved in the predisposition to systemic lupus erythematosus (SLE). The presence of low binding alleles in patients with SLE is not sufficient to explain the lower phagocytic capacity observed in SLE patients. We considered the possibility that nucleotide polymorphisms in the FcgammaRIIA promoter that cause alterations in receptor expression might be present in SLE patients. In the present study, a 2.0 kb region of the human FcgammaRIIA 5'UTR from 20 normal donors and 53 SLE patients was examined. The results demonstrate that the sequence of the human FcgammaRIIA 5' region differs from the published sequence. Two novel SNPs have been identified in the distal region of the FcgammaRIIA promoter. The polymorphisms are present in both disease-free and SLE donors and do not associate with quantitative changes in FcgammaRIIa phagocytic function.
FcγRIIA是一个与系统性红斑狼疮(SLE)易感性相关的候选基因。SLE患者中低结合等位基因的存在不足以解释在SLE患者中观察到的较低吞噬能力。我们考虑了SLE患者中可能存在FcγRIIA启动子中的核苷酸多态性导致受体表达改变的可能性。在本研究中,检测了20名正常供体和53名SLE患者的人FcγRIIA 5'非翻译区的2.0 kb区域。结果表明,人FcγRIIA 5'区域的序列与已发表的序列不同。在FcγRIIA启动子的远端区域鉴定出两个新的单核苷酸多态性(SNP)。这些多态性在无疾病供体和SLE供体中均存在,并且与FcγRIIa吞噬功能的定量变化无关。