Illegitimate expression of apolipoprotein A-II in Caco-2 cells is due to chromatin organization

Exp Cell Res. 1999 Mar 15;247(2):373-9. doi: 10.1006/excr.1998.4371.

Abstract

Transcriptional activity of the human apolipoprotein (apo) A-II promoter has been reported in transiently transfected Caco-2 cells, but not in the intestine in vivo. In the present study we established that the transcription of a stably transfected reporter gene under the control of the -911/+29 human apo A-II, decreases with the onset of the differentiation process. This decrease paralleled that of the expression of the endogenous apo A-II gene. The decrease in apo A-II expression is also followed by a marked increase in the expression of the intestine-specific apo A-IV gene, analyzed here as a marker of enterocytic differentiation. Using clonal glucose metabolic variants of Caco-2 cells we have also observed that the lowest levels of apo A-II mRNA are associated with the lowest rates of glucose consumption. The illegitimate apo A-II transcriptional activity observed in Caco-2 cells is linked to the presence of DNase-I hypersensitive sites within the enhancer. This reflects a chromatin organization which allows, in Caco-2 cells as in the liver, the communication between the apo A-II enhancer and the proximal promoter, unlike what is observed in intestinal epithelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoprotein A-II / genetics*
  • Caco-2 Cells
  • Chromatin*
  • Deoxyribonuclease I
  • Gene Expression Regulation*
  • Humans
  • Transcription, Genetic

Substances

  • Apolipoprotein A-II
  • Chromatin
  • Deoxyribonuclease I