Dynamic interplay of transcriptional machinery and chromatin regulates "late" expression of the chemokine RANTES in T lymphocytes

Mol Cell Biol. 2007 Jan;27(1):253-66. doi: 10.1128/MCB.01071-06. Epub 2006 Oct 30.

Abstract

The chemokine RANTES (regulated upon activation normal T cell expressed and secreted) is expressed "late" (3 to 5 days) after activation in T lymphocytes. In order to understand the molecular events that accompany changes in gene expression, a detailed analysis of the interplay between transcriptional machinery and chromatin on the RANTES promoter over time was undertaken. Krüppel-like factor 13 (KLF13), a sequence-specific DNA binding transcription factor, orchestrates the induction of RANTES expression in T lymphocytes by ordered recruitment of effector molecules, including Nemo-like kinase, p300/cyclic AMP response element binding protein (CBP), p300/CBP-associated factor, and Brahma-related gene 1, that initiate sequential changes in phosphorylation and acetylation of histones and ATP-dependent chromatin remodeling near the TATA box of the RANTES promoter. These events recruit RNA polymerase II to the RANTES promoter and are responsible for late expression of RANTES in T lymphocytes. Therefore, KLF13 is a key regulator of late RANTES expression in T lymphocytes.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / physiology*
  • Chemokine CCL5 / biosynthesis*
  • Chemokine CCL5 / genetics
  • Chromatin / chemistry
  • Chromatin / metabolism*
  • Gene Expression Regulation*
  • Humans
  • Kinetics
  • Kruppel-Like Transcription Factors / genetics
  • Kruppel-Like Transcription Factors / physiology*
  • Lymphocyte Activation
  • Models, Biological
  • Promoter Regions, Genetic
  • RNA Polymerase II / metabolism
  • RNA, Small Interfering / metabolism
  • Repressor Proteins / genetics
  • Repressor Proteins / physiology*
  • T-Lymphocytes / metabolism*
  • Time Factors
  • Transcription, Genetic*
  • p300-CBP Transcription Factors / metabolism

Substances

  • Cell Cycle Proteins
  • Chemokine CCL5
  • Chromatin
  • KLF13 protein, human
  • Kruppel-Like Transcription Factors
  • RNA, Small Interfering
  • Repressor Proteins
  • p300-CBP Transcription Factors
  • RNA Polymerase II