Tumor cells frequently show a lack of surface class-I major histocompatibility complex (MHC) antigen expression. These molecules are key recognition structures for immune rejection of tumor cells and their absence at the surface of tumor cells could favor the progression of tumors. We have analyzed
Shared regulatory elements in the promoters of MHC class I and class II genes
β Scribed by Peter J van den Elsen; Ad Peijnenburg; Marja C.J.A van Eggermond; Sam J.P Gobin
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 432 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0167-5699
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β¦ Synopsis
ranscription of major histocompatibility complex (MHC) class II genes is controlled by a number of transcription factors that interact with a set of conserved cisacting regulatory elements within the promoter region of MHC class II genes. These regulatory sequences include the W/S, X1, X2 and Y-box elements, and are important for both the constitutive and the interferon-β₯ (IFN-β₯)-induced expression of MHC class II genes (reviewed in Ref. 1) (Fig. ). A number of DNA-binding proteins bind to these conserved sequences including the RFX complex, which binds to the X1 box; X2BP, which binds to the X2 box; and NF-Y, which binds to the Y box (reviewed in Ref. 1). There are several lines of evidence to suggest a mutual interdependency of the transcription factors RFX, X2BP and NF-Y in the formation of DNA-protein complexes on the W/S-X-Y region in the MHC class II promoter 2 .
Likewise, a series of conserved DNA sequences in the MHC class I gene promoter play a crucial role in the constitutive and cytokineinduced regulation of transcription (reviewed in Ref. 3). They include the enhancer A (enhA), the IFN-stimulated response element (ISRE), site β£ and enhancer B (enhB) (Fig. ). These regulatory elements map within the first 250 base pairs (bp) of the MHC class II and class I promoters, immediately upstream of the transcription initiation site.
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