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通过DQA和DQB可变外显子的基因扩增对HLA - DQ等位基因进行DNA分型:DQA/DQB单倍型分析

DNA typing of HLA-DQ alleles by gene amplification of DQA and DQB variable exons: analysis of DQA/DQB haplotypes.

作者信息

Pera C, Delfino L, Angelini G, Longo A, Ferrara G B

机构信息

Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.

出版信息

Eur J Immunogenet. 1992 Dec;19(6):373-80. doi: 10.1111/j.1744-313x.1992.tb00080.x.

Abstract

In the present report, we describe a DNA typing method that allows detection of all the polymorphic variants of DQA1 and DQB1 second exons. By the oligotyping procedure provided in this paper, we are able to identify 8 DQA1 and 13 DQB1 alleles and to type random individuals in any heterozygous combination. We provide the hybridization and washing temperatures for using either 32P labelled or non-radioactive probes. The discrimination power of this procedure, compared to serological and cellular techniques, is remarkable. Therefore, this typing method finds perfect application in transplantation immunology and it will be very helpful to optimize the matching of unrelated donors before BMT. It is apparent from our results that despite the linkage disequilibrium present between DQ and DR loci, a DR specificity may frequently be associated to different DQ haplotypes. This is the case for DR4, DR7, DR8, DR9, and DR13 specificities.

摘要

在本报告中,我们描述了一种DNA分型方法,该方法能够检测DQA1和DQB1第二外显子的所有多态性变体。通过本文提供的寡核苷酸分型程序,我们能够鉴定出8个DQA1等位基因和13个DQB1等位基因,并对任何杂合组合的随机个体进行分型。我们提供了使用32P标记探针或非放射性探针的杂交和洗涤温度。与血清学和细胞技术相比,该程序的鉴别能力非常显著。因此,这种分型方法在移植免疫学中得到了完美应用,并且对于优化异基因骨髓移植前无关供体的匹配将非常有帮助。从我们的结果可以明显看出,尽管DQ和DR位点之间存在连锁不平衡,但一种DR特异性可能经常与不同的DQ单倍型相关。DR4、DR7、DR8、DR9和DR13特异性就是这种情况。

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