Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1927137 | Archives of Biochemistry and Biophysics | 2007 | 10 Pages |
Abstract
Carbohydrate response element binding protein (ChREBP) is a transcription factor that activates liver glycolytic and lipogenetic enzyme genes in response to high carbohydrate diet. Here we report the transcriptional regulatory mechanisms for the rat ChREBP gene. Firstly, we determined the transcription initiation site and the nucleotide sequences of the rat ChREBP promoter region encompassing approximately 900Â bp from the ATG initiation codon. Reporter gene assays demonstrated that the major positive regulatory region exists in the nucleotide sequence between â163 and â32 of the ChREBP gene. This region contains a cluster of putative transcription factor binding elements that consist of two specificity protein 1 (Sp1) binding sites (â66 to â50 and â93 to â78), a sterol regulatory element (â101 to â110), and two nuclear factor-Y (NF-Y) binding sites (â23 to â19 and â131 to â127). Mutations introduced into these sites caused marked reduction of ChREBP promoter activities. Functional synergisms were observed between Sp1/NF-Y and Sp1/sterol regulatory element-binding protein. Additionally, electrophoretic mobility shift assays and chromatin immunoprecipitation assays demonstrated that these factors bound to these elements. Thus, we conclude that functional synergisms between these transcription factors are critical for ChREBP gene transcription.
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Authors
Shin-ichi Satoh, Sakie Masatoshi, Zhangfei Shou, Taichi Yamamoto, Tatsuya Ishigure, Atsushi Semii, Kazuya Yamada, Tamio Noguchi,