Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10771122 | Biochemical and Biophysical Research Communications | 2005 | 8 Pages |
Abstract
To clarify the mechanisms and factors involved in the regulation of mouse IL-2Rβ gene expression, we isolated the 5â²-flanking region of IL-2Rβ gene and investigated the promoter activity. Here we elucidated the positive regulatory regions, the most potent of which are located between â50 to â30 bp and â164 to â135 bp. These regions contain a potentially functional Ets and Egr-1-binding sites whose mutations abrogate promoter activity. Data from electrophoretic mobility shift assay indicate that Ets and Egr-1, but not Sp1, bind to the positive regulatory regions, â50 to â30 bp and â164 to â135 bp, respectively. Furthermore, recruitment of Ets and Egr-1 at endogenous IL-2Rβ promoter segments in an IL-2-dependent F7 cells was verified by the chromatin immunoprecipitation assay. This study for the first time delineates the molecular mechanisms underlying regulation of mouse IL-2Rβ gene transcription by Ets family proteins, partially with Egr-1, and thereby further elucidates the molecular basis of lymphocyte activation and differentiation.
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Authors
Sang-Kyu Ye, Tack Joong Kim, Sung Sik Won, Taek Joon Yoon, Tae Kyu Park, Yung Choon Yoo, Yong-Nyun Kim, Hai Chon Lee, Koichi Ikuta, Myung-Hee Chung, Kwang Ho Lee,