Negative regulation of the gene for H-2Kb class I antigen by adenovirus 12-E1A is mediated by a CAA repeated element
Autor: | Alain Israël, K. Shiroki, Kazuo Ozawa, Kazushige Yokoyama, H. Hagiwara, Gabriel Gachelin, F. Saka, Kei Fujinaga, I. Kitabayashi, Xiaoren Tang |
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Rok vydání: | 1993 |
Předmět: |
Gene Expression Regulation
Viral DNA Complementary Negative regulatory element Molecular Sequence Data Genes MHC Class I Biology Major histocompatibility complex Biochemistry Binding Competitive Mice Antigen Cricetinae MHC class I Animals Promoter Regions Genetic Molecular Biology Gene Cells Cultured Repetitive Sequences Nucleic Acid Sequence Deletion Expression vector Base Sequence H-2 Antigens Nuclear Proteins Promoter Cell Biology Molecular biology Phosphoric Monoester Hydrolases Rats Regulatory sequence biology.protein Adenovirus E1A Proteins |
Zdroj: | The Journal of biological chemistry. 268(36) |
ISSN: | 0021-9258 |
Popis: | Both positive and negative regulatory elements responsive to the product of the adenovirus type 12 E1A gene are located in the promoter region of the gene for mouse H-2Kbm1 major histocompatibility complex (MHC) class I antigen (1). We have analyzed the negative regulatory element that is affected by E1A and identified a target CAA repeated motif, CAA(A)CAAA, within -1725 to -1705 and -1591 to -1568 in a 316-bp sequence located in the far upstream region of H-2Kb promoter (-1837 to -1522; +1 refers to the cap site). The extent of cell surface expression of the MHC class 1 antigen was significantly decreased in the case of transfectants obtained by introducing an expression plasmid that included MHC class 1 cDNA with the CAA repeated element, as compared with that of a plasmid with mutated CAA repeats. We have also characterized the nuclear proteins that bind to this motif. The analysis of the effects of mutations during competition assays of in vivo and gel retardation competition assays demonstrated that the CAA repeated element is essential not only for E1A-dependent repression of transcription but also for the cell surface expression of the product of the mouse H-2Kb class I gene, presumably through nuclear proteins that specifically bind to it. |
Databáze: | OpenAIRE |
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