Regulatory elements in the rat betaB2-crystallin promoter

Exp Eye Res. 2001 Nov;73(5):703-10. doi: 10.1006/exer.2001.1077.

Abstract

The suggested common regulator of the eye lens crystallin genes is c-Maf. Maf responsive elements have been detected in a number of crystallin promoters including that of the rat betaB2-crystallin gene. The betaB2-crystallin gene is active in the post-natal lens and its mRNA reaches its maximal level in the rat lens 6 months after birth. Yet c-Maf has been reported to be present in the rat lens only up to 3 months of age. This discrepancy prompted an investigation into the role of the Maf responsive element (MARE) in the regulation of activity of the rat betaB2-crystallin promoter in rat lens fiber cells. Although betaB2 promoter activity is enhanced by c-Maf in both in vitro differentiating rat lens fiber cells and CHO cells, deletion of the betaB2 MARE, which was mapped to -143/-123, does not decrease betaB2 promoter activity in lens fiber cells. Furthermore, a dominant negative c-Maf construct did not inhibit activity of the betaB2 promoter in lens fiber cells. The data suggest that the betaB2 MARE does not play a major role in regulating activity of the betaB2 promoter. Rather, a putative Sox binding site at -164/-159 and a positive element at -14/-7 seem to be the prime regulatory elements.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Crystallins / genetics*
  • Epithelial Cells / cytology
  • Fungal Proteins / genetics
  • Gene Expression
  • Genes, Regulator / physiology*
  • Genes, Reporter / physiology
  • Lens, Crystalline / metabolism
  • Promoter Regions, Genetic / physiology*
  • Rats
  • Saccharomyces cerevisiae Proteins*
  • Transcription Factors*
  • Transfection / methods

Substances

  • Crystallins
  • Fungal Proteins
  • MAF1 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors