Regulation of NKG2D ligand gene expression

被引:86
作者
Eagle, Robert A.
Traherne, James A.
Ashiru, Omodele
Wills, Mark R.
Trowsdale, John
机构
[1] Addenbrookes Hosp, Cambridge Inst Med Res, Cambridge CB2 2XY, England
[2] Univ Cambridge, Sch Clin, Dept Med, Cambridge, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
NKG2D; ligand; NK cell; promoter; HCMV; polymorphism;
D O I
10.1016/j.humimm.2006.02.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The activating immunoreceptor NKG2D has seven known host ligands encoded by the MHC class I chain-related MIC and ULBP/RAET genes. Why there is such diversity of NKG2D ligands is not known but one hypothesis is that they are differentially expressed in different tissues in response to different stresses. To explore this, we compared expression patterns and promoters of NKG2D ligand genes. ULBP/RAET genes were transcribed independent of each other in a panel of cell lines. ULBP/RAET gene expression was upregulated on infection with human cytomegalovirus; however, a clinical strain, Toledo, induced expression more slowly than did a laboratory strain, AD169. ULBP4/RAETIE was not induced by infection with either strain. To investigate the mechanisms behind the similarities and differences in NKG2D ligand gene expression a comparative sequence analysis of NKG2D ligand gene Putative promoter regions was conducted. Sequence alignments demonstrated that there was significant sequence diversity; however, one region of high similarity between most of the genes is evident. This region contains a number of potential transcription factor binding sites, including those involved in shock responses and sites for retinoic acid-induced factors. Promoters of some NKG2D ligand genes are polymorphic and several sequence alterations in these alleles abolished Putative transcription factor binding.
引用
收藏
页码:159 / 169
页数:11
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