IL-10 gene expression is controlled by the transcription factors Sp1 and Sp3

被引:223
作者
Tone, M [1 ]
Powell, MJ [1 ]
Tone, Y [1 ]
Thompson, SAJ [1 ]
Waldmann, H [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
关键词
D O I
10.4049/jimmunol.165.1.286
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-10 is an 18-kDa cytokine with a key role in homeostatic control of inflammatory and immune responses. We have investigated how transcription of the IL-10 gene is regulated, so as to be able to understand the circumstances of IL-10 expression in both health and disease. In the mouse, IL-10 gene expression is regulated by a TATA-type promoter with a critical cis-acting element containing GGA repeats located at -89 to -77. Its complementary sequence is similar to the cis-acting elements (TCC repeats) in the promoters of genes encoding epidermal growth factor receptor and Cuss, All these elements comprise a common CCTCCT sequence with less conserved C + T-rich sequences, Eliminating this CCTCCT sequence results in a marked reduction in promoter activity, suggesting a necessary role in IL-10 gene expression. Despite its dissimilarity to the G + C-rich Spl consensus sequence (GC box), Sp1 and Sp3 transcription factors could be shown to bind to this motif, The requirement for Sp1 and Sp3 in transcription of IL-10 was confirmed using Drosophila SL2 cells, which lack endogenous Sp factors. These results suggest that the transcription of IL-10 is positively regulated by both Sp1 and Sp3.
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页码:286 / 291
页数:6
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