MHC class II enhanceosome: how is the class II transactivator recruited to DNA-bound activators?

被引:48
作者
Jabrane-Ferrat, N
Nekrep, N
Tosi, G
Esserman, L
Peterlin, BM
机构
[1] Univ Calif San Francisco, Dept Surg, San Francisco, CA 94115 USA
[2] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94115 USA
[3] Univ Calif San Francisco, Rosalind Russell Med Res Ctr, San Francisco, CA 94115 USA
[4] Univ Calif San Francisco, Dept Med, San Francisco, CA 94115 USA
[5] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94115 USA
[6] Univ Ljubljana, Fac Med, Inst Biochem, Ljubljana, Slovenia
[7] Univ Insubria, Dept Clin & Biol Sci, Varese, Italy
关键词
activator; assembly; nuclear factor Y; regulatory factor X; transcription;
D O I
10.1093/intimm/dxg048
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MHC class II (MHCII) determinants play a crucial role in the immune response by presenting antigenic peptides to T cells. Their expression is controlled from compact promoters at the transcriptional level. Pre-assembled regulatory factor X (RFX) and nuclear factor Y (NFY) complexes form a platform on DNA. The class II transactivator (CIITA) can then be recruited through multiple protein-protein interactions. In this report, we defined domains of CIITA that are responsible for its interactions with these DNA-bound factors. Furthermore, using DNA-affinity precipitation, we demonstrated that although CIITA binds at least five activators, RFX5, RFXAP, RFXANK/B, NFYB and NFYC, its assembly on the promoter requires the addition of nuclear extracts. We conclude that not only does the platform bind DNA via multiple, spatially constrained nteractions, but that it can recruit only modified and/or complexed CIITA to MHCII promoters.
引用
收藏
页码:467 / 475
页数:9
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