Downregulation of constitutive and heavy metal-induced metallothionein-I expression by nuclear factor I

Gene Expr. 2001;9(4-5):203-15. doi: 10.3727/000000001783992588.

Abstract

Although the existence of repressor protein(s) involved in the regulation of highly inducible metallothionein-I (MT-I) gene expression has been postulated, none has been identified to date. We considered nuclear factor I (NFL) protein as a potential repressor, as three half-sites for NFI binding are present on MT-I promoter and NFI is known to downregulate several cellular gene promoters. Overexpression of all four isoforms of mouse NFI protein (NFI-A, -B, -C, and -X) suppressed both constitutive and heavy metal-induced activation of the MT-I promoter in HepG2 cells. However, unlike other target genes of NFI, direct interaction of NFI with MT-I promoter is not necessary to mediate its repression. Point mutation of the NFI binding sites within the MT-I promoter that abrogates NFI binding in vitro could not alleviate the repression. Similarly, NFI proteins also repress activity of minimal MT-I promoter deficient in the NFI binding sites. Further, an NFI-C deletion mutant lacking the DNA binding domain continued to repress MT-I promoter. Overexpression of MTF-1, the key trails-acting factor involved in MT-I gene transcription, surmounted NFI-mediated repression of the basal and zinc-induced MT-I promoter activity. These data demonstrate that NFI is a repressor of MT-I expression, where its DNA binding activity is not essential to downregulate the MT-I promoter. Interaction of NFI with another protein(s), probably MTF-I, may be involved in this repression.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • CCAAT-Enhancer-Binding Proteins / genetics
  • CCAAT-Enhancer-Binding Proteins / metabolism*
  • Cadmium / pharmacology
  • Cells, Cultured
  • DNA / genetics
  • DNA / metabolism
  • DNA-Binding Proteins*
  • Down-Regulation* / drug effects
  • Electrophoretic Mobility Shift Assay
  • Luciferases / genetics
  • Luciferases / metabolism
  • Metallothionein / genetics*
  • Metals, Heavy / pharmacology*
  • Mice
  • Mutation / genetics
  • NFI Transcription Factors
  • Nuclear Proteins
  • Promoter Regions, Genetic / genetics
  • Rats
  • Repressor Proteins / metabolism
  • Response Elements / genetics
  • Transcription Factor MTF-1
  • Transcription Factors / metabolism
  • Transfection
  • Y-Box-Binding Protein 1

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DNA-Binding Proteins
  • Metals, Heavy
  • NFI Transcription Factors
  • Nfia protein, mouse
  • Nfic protein, mouse
  • Nfic protein, rat
  • Nuclear Proteins
  • Repressor Proteins
  • Transcription Factors
  • Y-Box-Binding Protein 1
  • YBX1 protein, human
  • Cadmium
  • DNA
  • Metallothionein
  • Luciferases