首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Detection of HLA-D/DR-related DNA polymorphism in HLA-D homozygous typing cells.
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Detection of HLA-D/DR-related DNA polymorphism in HLA-D homozygous typing cells.

机译:检测HLA-D纯合型细胞中HLA-D / DR相关的DNA多态性。

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摘要

Sequences of different sizes are generated when DNA from homozygous HLA-Dw/DR typing cells are digested with restriction endonuclease and analyzed by hybridization with a HLA-D region class II antigen beta-chain cDNA probe. The patterns of hybridization were highly polymorphic but one endonuclease, BamHI, defined sequences unique to all HLA-Dw/DR specificities 1-8 except HLA-Dw/DR 2 and 6; however, these two specificities were resolved with the enzyme EcoRI. Digestion with other endonucleases such as Pst I results in patterns of restriction fragments that differ between homozygous typing cells of the same HLA-Dw/DR specificity. HLA-D region beta-chain probes permit HLA-D region genotyping at the DNA level and may allow detection of genes controlling the association of HLA specificities with a wide variety of diseases.
机译:当用限制性核酸内切酶消化来自纯合HLA-Dw / DR分型细胞的DNA并通过与HLA-D II类抗原B链cDNA探针杂交进行分析时,会产生不同大小的序列。杂交的模式是高度多态的,但一种核酸内切酶BamHI定义了除HLA-Dw / DR 2和6以外的所有HLA-Dw / DR特异性1-8特有的序列;但是,这两种特异性已通过酶EcoRI得以解决。用其他核酸内切酶(例如Pst I)消化会产生限制性片段的模式,这些片段在具有相同HLA-Dw / DR特异性的纯合型细胞之间会有所不同。 HLA-D区β链探针可在DNA水平进行HLA-D区基因分型,并可检测控制HLA特异性与多种疾病相关的基因。

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