Transcriptional control of Nramp1: a paradigm for the repressive action of c-Myc

Biochem Soc Trans. 2004 Dec;32(Pt 6):1084-6. doi: 10.1042/BST0321084.

Abstract

Slc11a1/Nramp1 (solute carrier family 11 member a1/murine natural resistance-associated macrophage protein 1 gene) encodes a divalent cation transporter that resides within lysosomes/late endosomes of macrophages. Nramp1 modulates the cellular distribution of divalent cations in response to cell activation by intracellular pathogens. Nramp1 expression is repressed and activated by the proto-oncogene c-Myc and Miz-1 (c-Myc-interacting zinc finger protein 1) respectively. Here we demonstrate, using a c-Myc mutant (V394D, Val(394)-->Asp) that is incapable of binding Miz-1, that c-Myc repression of Nramp1 transcription is dependent on its interaction with Miz-1. An oligo pull-down assay demonstrates specific binding of recombinant Miz-1 to the Nramp1 Miz-1-binding site or initiator element(s), and Miz-1-dependent c-Myc recruitment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cation Transport Proteins / genetics*
  • Cations, Divalent
  • Cell Physiological Phenomena
  • Genes, myc*
  • Genetic Vectors
  • Models, Genetic
  • Restriction Mapping
  • Transcription, Genetic*

Substances

  • Cation Transport Proteins
  • Cations, Divalent
  • natural resistance-associated macrophage protein 1