The bcl-2 major breakpoint region (mbr) possesses transcriptional regulatory function

Gene. 2006 Sep 1:379:127-31. doi: 10.1016/j.gene.2006.05.002. Epub 2006 May 9.

Abstract

The bcl-2 major breakpoint region (mbr), located within the 3'-UTR of the bcl-2 gene, is the site of the most common chromosomal translocation, t(14;18) (q32;q21), which occurs in follicular lymphoma. The mbr forms a triplex DNA structure under physiological conditions and the transcription factor special AT-rich sequence-binding protein 1 (SATB1) binds immediately downstream of the mbr. These observations raise the possibility that the mbr may be involved in regulation of bcl-2 gene expression. We investigated the role of the bcl-2 mbr on reporter gene activity and the relevance of SATB1 to this function in a variety of cell lines. We found that the mbr up-regulated reporter gene expression. Deletion of the 37-bp AT-rich SATB1 binding site abolished the bcl-2 mbr regulation of reporter gene expression. Overexpression of SATB1 enhanced bcl-2 mbr up-regulation of the reporter gene activity. Our data strongly demonstrated that the bcl-2 mbr possessed regulatory function that was related to SATB1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / chemistry
  • Binding Sites
  • Cell Line, Tumor
  • Female
  • Genes, Reporter
  • Humans
  • Jurkat Cells
  • Luciferases / genetics
  • Luciferases / metabolism
  • Lymphocytes
  • Matrix Attachment Region Binding Proteins / genetics
  • Matrix Attachment Region Binding Proteins / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / genetics*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Transcription, Genetic*
  • Transfection

Substances

  • 3' Untranslated Regions
  • Matrix Attachment Region Binding Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • SATB1 protein, human
  • Luciferases