Parsons S F, Mallinson G, Daniels G L, Green C A, Smythe J S, Anstee D J
International Blood Group Reference Laboratory, Bristol Institute for Transfusion Sciences, UK.
Blood. 1997 Jun 1;89(11):4219-25.
Lutheran glycoprotein (Lu gp) has five predicted immunoglobulin superfamily (IgSF) domains. K562 cells were transfected with Lu cDNA and tested by flow cytometry with monoclonal antibodies and Lu blood group antisera. The results confirmed the identity of Lu cDNA. Deletion mutants lacking the regions encoding one or more IgSF domains were made by inverse polymerase chain reaction (PCR), expressed in K562 cells, and tested with the same antibodies. The Lu(b) and Lu5 antigens and the epitope recognized by monoclonal antibody BRIC 224 were mapped to the first, N-terminal, IgSF domain. Lu4 and Lu8 were mapped to domain 2; Lu20 to domain 3; Lu7 and BRIC 221 epitope to domain 4, and Lu13 and Au(b) to domain 5. The organization of the LU gene was determined. The region encoding the open reading frame is arranged in 15 exons extending over approximately 11 kb on chromosome 19q13.2. The Lu(a)/Lu(b) and Au(a)/Au(b) blood group polymorphisms were studied using genomic DNA from typed blood donors. The Lu(a) mutation is a base change in exon 3 (G252 to A) encoding an Arg77 (Lu(b)) to His (Lu(a)) change on the CFG face of domain 1. The Au(a)/Au(b) polymorphism is an A1637 to G substitution in exon 12 encoding a Thr539 (Au(a)) to Ala (Au(b)) change on the G strand of domain 5.
路德糖蛋白(Lu gp)有五个预测的免疫球蛋白超家族(IgSF)结构域。用Lu cDNA转染K562细胞,并用单克隆抗体和Lu血型抗血清进行流式细胞术检测。结果证实了Lu cDNA的一致性。通过反向聚合酶链反应(PCR)构建缺失一个或多个IgSF结构域编码区的缺失突变体,在K562细胞中表达,并用相同抗体进行检测。Lu(b)和Lu5抗原以及单克隆抗体BRIC 224识别的表位被定位到第一个N端IgSF结构域。Lu4和Lu8被定位到结构域2;Lu20被定位到结构域3;Lu7和BRIC 221表位被定位到结构域4,Lu13和Au(b)被定位到结构域5。确定了LU基因的结构。编码开放阅读框的区域由15个外显子组成,分布在19号染色体q13.2上约11 kb的区域。使用来自血型分型献血者的基因组DNA研究了Lu(a)/Lu(b)和Au(a)/Au(b)血型多态性。Lu(a)突变是外显子3中的碱基变化(G252突变为A),导致结构域1的CFG面上的精氨酸77(Lu(b))变为组氨酸(Lu(a))。Au(a)/Au(b)多态性是外显子12中的A1637到G的替换,导致结构域5的G链上的苏氨酸539(Au(a))变为丙氨酸(Au(b))。