Morzycka-Wroblewska E, Harwood J I, Smith J R, Kagnoff M F
Department of Medicine, University of California, San Diego, La Jolla 92093-0623.
Immunogenetics. 1993;37(5):364-72. doi: 10.1007/BF00216801.
HLA-DQ antigens are unique among the class II antigens in that their alpha chains are highly polymorphic. In the present study, we characterized the general structure of the promoter regions of the DQA genes derived from different DR haplotypes and defined their nucleotide sequence polymorphisms. The promoter of each DQA1 allele contains three sequence motifs which are not present in non-DQA related class II genes: one identical to a tumor necrosis factor (TNF alpha) response element, one similar to an NF kappa B binding element, and one similar to a W motif. All DQA alleles lack TATA and CCAAT boxes in the proximal promoter region but carry other sequence elements characteristic of MHC class II genes, including S, X, X2, and Y boxes, and a pyrimidine-rich tract upstream of the X box. Nucleotide sequence polymorphisms among the various DQA1 alleles were noted within the promoter region, with some of the differences mapping within, or close to, regulatory elements that are important for the expression of MHC class II genes. All DQA1 alleles carry an unrearranged, full length, Alu-Sx related repeat immediately upstream of the proximal promoter region. This repeat was not present in the DQA2 (DXA) genes analyzed, confirming that DQ locus duplication probably occurred before integration of the Alu repeat into the primordial DQA1 locus, some 31-43 million years (myr) ago. The DQA2 promoter region is highly conserved between DR4 and DR3 haplotypes, with the degree of conservation exceeding that expected from the neutral mutation rate.
HLA-DQ抗原在Ⅱ类抗原中独具特色,因为其α链具有高度多态性。在本研究中,我们对源自不同DR单倍型的DQA基因启动子区域的总体结构进行了表征,并确定了它们的核苷酸序列多态性。每个DQA1等位基因的启动子包含三个在非DQA相关的Ⅱ类基因中不存在的序列基序:一个与肿瘤坏死因子(TNFα)反应元件相同,一个与NFκB结合元件相似,还有一个与W基序相似。所有DQA等位基因在近端启动子区域都缺乏TATA盒和CCAAT盒,但带有其他MHCⅡ类基因特有的序列元件,包括S盒、X盒、X2盒和Y盒,以及X盒上游的富含嘧啶的区域。在启动子区域内发现了各种DQA1等位基因之间的核苷酸序列多态性,其中一些差异位于对MHCⅡ类基因表达很重要的调控元件内或其附近。所有DQA1等位基因在近端启动子区域上游紧邻处都带有一个未重排的、全长的、与Alu-Sx相关的重复序列。在所分析的DQA2(DXA)基因中不存在这种重复序列,这证实了DQ基因座的复制可能发生在大约3100万至4300万年前Alu重复序列整合到原始DQA1基因座之前。DQA2启动子区域在DR4和DR3单倍型之间高度保守,其保守程度超过了中性突变率所预期的程度。