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利用将DR基因导入小鼠L细胞的方法对DR2抗原的基因结构和抗原决定簇进行分析。

Analysis of gene structure and antigen determinants of DR2 antigens using DR gene transfer into mouse L cells.

作者信息

Kawai J, Ando A, Sato T, Nakatsuji T, Tsuji K, Inoko H

机构信息

Department of Transplantation, Tokai University School of Medicine, Kanagawa, Japan.

出版信息

J Immunol. 1989 Jan 1;142(1):312-7.

PMID:2462589
Abstract

Three HLA class II DR beta genes and one DR alpha gene from the DR2 haplotype were cloned in cosmid vectors. The DR beta II gene might be a pseudogene lacking the first exon that encodes the leader peptide. The DR beta I and DR beta III genes were expressed, together with the DR alpha-chain, after transfection into mouse L cells. Restriction enzyme mapping of the DR beta genomic clones and reactivity of their products expressed on the L cell transfectant against mAb showed that the DR beta I and DR beta III genes encoded the nonpolymorphic and polymorphic DR beta chain, respectively. This arrangement is the reverse of that observed in other haplotypes, such as DR3, 4 and 6. The alignment of the HLA class II genes including the DR beta genes on the chromosome 6, however, was consistent with other haplotypes, e.g., centromere-DX beta-DX alpha-DV beta-DQ beta-DQ alpha-DR beta I-DR beta II- DR beta III-DR alpha-telomere. These results suggest that the susceptibility to mutations or gene conversions responsible for genetic polymorphisms depends on the gene itself and not on its location. Furthermore, absorption experiments of anti-DR2 allosera by the DR alpha/DR beta transfectants revealed that the so-called DR2 specificities were determined by multiple epitopes although both the DR beta I and DR beta III genes behaved similarly with DR2-specific antibodies.

摘要

从DR2单倍型中克隆出三个HLA - II类DRβ基因和一个DRα基因,并将其克隆到黏粒载体中。DRβII基因可能是一个假基因,缺少编码前导肽的第一个外显子。将DRβI和DRβIII基因与DRα链一起转染到小鼠L细胞后,它们得以表达。对DRβ基因组克隆进行限制性酶切图谱分析,以及其在L细胞转染体上表达的产物与单克隆抗体的反应性表明,DRβI和DRβIII基因分别编码非多态性和多态性的DRβ链。这种排列与在其他单倍型(如DR3、4和6)中观察到的情况相反。然而,包括6号染色体上的DRβ基因在内的HLA - II类基因的排列与其他单倍型一致,例如着丝粒 - DXβ - DXα - DVβ - DQβ - DQα - DRβI - DRβII - DRβIII - DRα - 端粒。这些结果表明,导致遗传多态性的突变或基因转换的易感性取决于基因本身而非其位置。此外,DRα/DRβ转染体对抗DR2同种异体血清的吸收实验表明,尽管DRβI和DRβIII基因与DR2特异性抗体的反应相似,但所谓的DR2特异性是由多个表位决定的。

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