Histone dynamics on the interleukin-2 gene in response to T-Cell activation

Xinxin Chen, Jun Wang, Donna Woltring, Steve Gerondakis, Frances Shannon

Research output: Contribution to journalArticlepeer-review

90 Citations (Scopus)


Several models have been proposed for the mechanism of chromatin remodelling across the promoters of inducible genes in mammalian cells. The most commonly held model is one of cooccupation where histone proteins are modified by acetylation or phosphorylation and nucleosomes are remodelled, allowing the assembly of transcription factor complexes. Using chromatin immunoprecipitation, we observed an apparent decrease of histone acetylation and phosphorylation signals at the proximal promoter region of the inducible interleukin-2 and granulocyte-macrophage colony-stimulating factor genes in response to T-cell activation. We showed that this apparent decrease was due to a loss of histone H3 and H4 proteins corresponding to a decrease in nucleosome occupation of the promoter. This histone loss is reversible; it is dependent on the continual presence of appropriate activating signals and transcription factors and is not dependent on the acetylation status of the histone proteins. These data show for the first time that histone proteins are lost from a mammalian promoter upon activation of transcription and support a model of activation-dependent disassembly and reassembly of nucleosomes
Original languageEnglish
Pages (from-to)3209-3219
Number of pages11
JournalMolecular and Cellular Biology
Issue number8
Publication statusPublished - 2005
Externally publishedYes


Dive into the research topics of 'Histone dynamics on the interleukin-2 gene in response to T-Cell activation'. Together they form a unique fingerprint.

Cite this