Cloning and characterization of the human PAX7 promoter

Biol Chem. 2000 Apr;381(4):331-5. doi: 10.1515/BC.2000.043.

Abstract

PAX7, a member of the PAX transcription factor gene family, is normally expressed at high levels during development in the neural tube and in skeletal muscle precursor cells. Interestingly, PAX7 expression was also identified in tumor cells developing from these cell types. To date not much is known about the molecular mechanisms controlling the regulation of PAX7 expression. Therefore, we have cloned and sequenced part of the proximal 5'-flanking region of the human PAX7 gene. Computer-based sequence analysis identified putative binding sites for basic transcription factors. Analysis of a series of deletion constructs in different cell types suggested that a distal region containing several E-boxes might be involved in muscle-specific expression of PAX7, and that a distinct proximal region can enhance basal PAX7 expression in tumor cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5' Untranslated Regions
  • Animals
  • Binding Sites
  • Cloning, Molecular*
  • Gene Deletion
  • Gene Expression Regulation
  • Genetic Engineering
  • Homeodomain Proteins / genetics*
  • Humans
  • Mice
  • Molecular Sequence Data
  • Muscle Proteins / genetics
  • Neoplasm Proteins / genetics
  • Nerve Tissue Proteins / genetics
  • PAX7 Transcription Factor
  • Promoter Regions, Genetic / genetics*
  • Sequence Analysis, DNA
  • Transcription Factors / genetics
  • Transfection
  • Tumor Cells, Cultured

Substances

  • 5' Untranslated Regions
  • Homeodomain Proteins
  • Muscle Proteins
  • Neoplasm Proteins
  • Nerve Tissue Proteins
  • PAX7 Transcription Factor
  • PAX7 protein, human
  • Pax7 protein, mouse
  • Transcription Factors