Regulation of the gene encoding glutathione S-transferase M1 (GSTM1) by the Myb oncoprotein

被引:13
作者
Bartley, PA
Keough, RA
Lutwyche, JK
Gonda, TJ
机构
[1] Inst Med & Vet Sci, Hanson Inst, Adelaide, SA 5000, Australia
[2] Inst Med & Vet Sci, Div Human Immunol, Adelaide, SA 5000, Australia
[3] Univ Adelaide, Dept Med, Adelaide, SA 5005, Australia
基金
英国医学研究理事会;
关键词
Myb; transactivation; glutathione S-transferase; promoter;
D O I
10.1038/sj.onc.1207136
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The identification of Myb 'target' genes will not only aid in the understanding of how overexpression of Myb, or expression of activated forms of Myb, leads to cellular transformation but will also shed light on its role in normal cells. Using a combination of an estrogen-regulated Myb-transformed cell line (ERMYB) and PCR-based subtractive hybridization, we have identified the gene (GSTM1) encoding the detoxification enzyme glutathione S-transferase M1 as being transcriptionally upregulated by Myb. Functional analysis of the GSTM1 promoter using reporter assays indicated that both the DNA binding and transactivation domains of Myb were required for transcriptional activation. Mutational analysis of consensus Myb-binding sites (MBS) in the promoter and electrophoretic mobility gel shift analysis indicated that one of the three potential MBS can bind Myb protein, and is the primary site involved in the regulation of this promoter by Myb.
引用
收藏
页码:7570 / 7575
页数:6
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