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通过与序列特异性寡核苷酸探针杂交对人类HLA - DR多态性进行高分辨率分析。

High-resolution analysis of the human HLA-DR polymorphism by hybridization with sequence-specific oligonucleotide probes.

作者信息

Angelini G, de Preval C, Gorski J, Mach B

出版信息

Proc Natl Acad Sci U S A. 1986 Jun;83(12):4489-93. doi: 10.1073/pnas.83.12.4489.

Abstract

The human major histocompatibility complex class II antigens of the HLA-D are highly polymorphic, surface proteins essential in the cellular interactions necessary for an immune response. The analysis of this polymorphism is crucial for (i) histocompatibility matching for transplantation and (ii) understanding the association between HLA-D and certain important diseases. The polymorphism of certain HLA-D haplotypes may escape detection by current methodologies. Analysis at the genomic level of the polymorphism of one of the HLA-D subregions HLA-DR, using oligonucleotide probes specific for the polymorphic regions, is capable of distinguishing single nucleotide differences. The DRw6 haplotype was analyzed in view of the lack of DRw6 specific sera. On the basis of nucleotide sequence analysis, the DRw6 haplotype consists of at least two subtypes. When analyzed with oligonucleotide probes, this split identifies new polymorphic groups that differ from the DRw6 serological subgroups.

摘要

HLA - D的人类主要组织相容性复合体II类抗原具有高度多态性,是免疫应答所需细胞相互作用中必不可少的表面蛋白。这种多态性分析对于(i)移植的组织相容性匹配和(ii)理解HLA - D与某些重要疾病之间的关联至关重要。某些HLA - D单倍型的多态性可能无法被当前方法检测到。使用针对多态性区域的寡核苷酸探针,在基因组水平分析HLA - D亚区域之一HLA - DR的多态性,能够区分单核苷酸差异。鉴于缺乏DRw6特异性血清,对DRw6单倍型进行了分析。基于核苷酸序列分析,DRw6单倍型至少由两个亚型组成。用寡核苷酸探针分析时,这种分型识别出了与DRw6血清学亚组不同的新的多态性组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2f2/323759/e122961acab4/pnas00316-0391-a.jpg

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