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HLA - A*0101无效等位基因的5'调控核苷酸序列。

5' regulatory nucleotide sequence of an HLA-A*0101null allele.

作者信息

Lardy N M, Otting N, van der Horst A R, Bontrop R E, de Waal L P

机构信息

Department of HLA Diagnostics, Central Laboratory of the Netherlands Red Cross Blood Transfusion Service and Laboratory for Experimental and Clinical Immunology of the University of Amsterdam, Plesmanlaan 125, 1066 CX, The Netherlands.

出版信息

Immunogenetics. 1997;46(2):152-5. doi: 10.1007/s002510050254.

Abstract

We have previously demonstrated an HLA-A0101null allele segregating in a family with the HLA-B8, -Cw7, -DR3, -DR52, -DQ2 haplotype. In the present study the regulatory elements with known transcription enhancement activity of the silenced HLA-A0101 allele were analyzed. In the enhancer B element, a T was substituted for a C at position - 106, whereas no other alterations were found in the adjacent 5' section of the HLA-A0101null allele. This substitution was not seen in the enhancer B elements of the corresponding genes involved in normal HLA-A0101 membrane expression. Comparison of enhancer B element sequences of classical functional major histocompatibility complex (MHC) class I alleles demonstrated a high degree of conservation. In contrast, many MHC class I pseudogenes showed mutation in their enhancer B boxes. These results may indicate that the single mutation detected in the enhancer B element plays a pivotal role in the abolishment of membrane expression of the HLA-A*0101null allele.

摘要

我们之前已证明,一个HLA - A0101无效等位基因在一个具有HLA - B8、- Cw7、- DR3、- DR52、- DQ2单倍型的家族中分离。在本研究中,对沉默的HLA - A0101等位基因具有已知转录增强活性的调控元件进行了分析。在增强子B元件中,第 - 106位的C被T取代,而在HLA - A0101无效等位基因相邻的5' 区域未发现其他改变。在参与正常HLA - A0101膜表达的相应基因的增强子B元件中未见到这种取代。经典功能性主要组织相容性复合体(MHC)I类等位基因的增强子B元件序列比较显示出高度保守性。相比之下,许多MHC I类假基因在其增强子B框中出现了突变。这些结果可能表明,在增强子B元件中检测到的单一突变在HLA - A*0101无效等位基因膜表达的消除中起关键作用。

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