Expression of MHC class II molecules in different cellular and functional compartments is controlled by differential usage of multiple promoters of the transactivator CIITA

被引:440
作者
MuhlethalerMOttet, A [1 ]
Otten, LA [1 ]
Steimle, V [1 ]
Mach, B [1 ]
机构
[1] UNIV GENEVA,SCH MED,DEPT GENET & MICROBIOL,L JEANTET LAB MOL GENET,CH-1211 GENEVA 4,SWITZERLAND
关键词
CIITA; MHC class II; promoter; transactivator; BARE LYMPHOCYTE SYNDROME; GENE-EXPRESSION; DNA-BINDING; REGULATORY FACTOR; NUCLEAR PROTEINS; SEQUENCES; INTERFERON; ENHANCER; IMMUNODEFICIENCY; TRANSCRIPTION;
D O I
10.1093/emboj/16.10.2851
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The highly complex pattern of expression of major histocompatibility complex class II (MHC-II) molecules determines both the immune repertoire during development and subsequently the triggering and the control of immune responses. These distinct functions result from cell type-restricted expression, developmental control and either constitutive or inducible expression of MHC-II genes, Yet, in these various situations, MHC-II gene expression is always under the control of a unique transactivator, CIITA. Here we show that the CIITA gene is controlled by several distinct promoters, two of which direct specific constitutive expression in dendritic cells and B lymphocytes respectively, while another mediates gamma-interferon-induced expression, Thus the cellular, temporal and functional diversity of MHC-II expression is ultimately controlled by differential activation of different promoters of a single transactivator gene, This provides novel experimental tools to dissect compartment-specific gain or loss of MHC-H function in vivo.
引用
收藏
页码:2851 / 2860
页数:10
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