c-Myc represses the murine Nramp I promoter

被引:7
作者
Bowen, H
Biggs, TE
Baker, ST
Phillips, E
Perry, VH
Mann, DA
Barton, CH
机构
[1] Univ Southampton, Cell Sci CNS Inflammat Grp, Southampton SO16 7PX, Hants, England
[2] Univ Southampton, Southampton Gen Hosp, Liver Grp, Div Cell & Mol Med, Southampton SO16 6YD, Hants, England
关键词
initiator element; macrophage; repression;
D O I
10.1042/bst0300774
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Nramp1 (natural resistance-associated macrophage protein 1) gene modulates the growth of intracellular pathogens and encodes a divalent cation transporter within lysosomes/late endosomes of macrophages. Nramp1 modulates the cytoplasmic iron pool. Wu, Polack and Dalla-Favera [(1999) Science 283, 676-679] showed reciprocal control of H-ferritin and IRP2 by c-Myc, and suggest that c-Myc regulates genes to increase cytoplasmic iron. A role for c-Myc in Nramp1 regulation was evaluated. Co-transfection studies show that c-Myc represses Nramp1 promoter function. Five non-canonical Myc-max binding sites (E-box) identified within the Nramp1 5'-flanking sequence are not responsible for the inhibitory effects of c-Myc on Nramp1 expression. An initiator(s) adjacent to the transcription-initiation site is a candidate for the inhibition observed. Results are consistent with a role for Nramp1 removing iron from the cytosol and antagonizing c-Myc function.
引用
收藏
页码:774 / 777
页数:4
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