Chromatin state and microRNA determine different gene expression dynamics responsive to TNF stimulation

Genomics. 2012 Nov;100(5):297-302. doi: 10.1016/j.ygeno.2012.07.009. Epub 2012 Jul 21.

Abstract

Gene expression is a dynamic process, and what factors influence gene expression changes upon external stimulus have not been clearly understood. We studied gene expression profiles in human umbilical vein endothelial cells (HUVEC) after the Tumor Necrosis Factor (TNF) stimulus, and found that: the promoters of fast-response up-regulated genes were enriched with several "active" chromatin markers like H3K27ac and H3K4me3, and also preferentially bound by Pol II and c-Myc; the core-promoter regions of slow-response up-regulated genes were frequently occupied by nucleosomes; down-regulated genes were more intensively regulated by microRNAs. Moreover, the Gene Ontology and motif analysis of the promoter regions revealed that gene clusters with different response behaviors had different functions and were regulated by different sets of transcription factors. Our observations suggested that the different gene expression patterns upon external stimulus were regulated by a combination of multi-layer regulators.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatin / genetics*
  • Computational Biology
  • Gene Expression Profiling
  • Gene Expression Regulation / drug effects*
  • Gene Expression Regulation / physiology
  • Genetic Markers / genetics
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • MicroRNAs / genetics*
  • Microarray Analysis
  • Multigene Family / genetics
  • Transcription Factors / genetics
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Chromatin
  • Genetic Markers
  • MicroRNAs
  • Transcription Factors
  • Tumor Necrosis Factor-alpha