Genome-wide analysis of Foxp3 target genes in developing and mature regulatory T cells (original) (raw)
- Letter
- Published: 21 January 2007
- Steven Z. Josefowicz2,
- Arnold Kas2,
- Tin-Tin Chu2,
- Marc A. Gavin2 nAff3 &
- …
- Alexander Y. Rudensky1,2
Nature volume 445, pages 936–940 (2007)Cite this article
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Abstract
Transcription factor Foxp3 (forkhead box P3), restricted in its expression to a specialized regulatory CD4+ T-cell subset (TR) with a dedicated suppressor function, controls TR lineage development. In humans and mice, Foxp3 deficiency results in a paucity of TR cells and a fatal breach in immunological tolerance, causing highly aggressive multi-organ autoimmune pathology1,2,3. Here, through genome-wide analysis combining chromatin immunoprecipitation with mouse genome tiling array profiling, we identify Foxp3 binding regions for ∼700 genes and for an intergenically encoded microRNA. We find that a large number of Foxp3-bound genes are up- or downregulated in Foxp3+ T cells, suggesting that Foxp3 acts as both a transcriptional activator and repressor. Foxp3-mediated regulation unique to the thymus affects, among others, genes encoding nuclear factors that control gene expression and chromatin remodelling. In contrast, Foxp3 target genes shared by the thymic and peripheral TR cells encode primarily plasma membrane proteins, as well as cell signalling proteins. Together, our studies suggest that distinct transcriptional sub-programmes implemented by Foxp3 establish TR lineage during differentiation and its proliferative and functional competence in the periphery.
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Acknowledgements
We thank K. Forbush and L. Karpik for assistance, and the members of our laboratory for discussions. This work was supported by the Cancer Research Institute (Y.Z.) and grants from the National Institutes of Health (A.Y.R.).
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- Marc A. Gavin
Present address: Present address: Amgen Corporation, Seattle, Washington 98101, USA.,
Authors and Affiliations
- Howard Hughes Medical Institute,,
Alexander Y. Rudensky - Department of Immunology, University of Washington, Seattle, Washington 98195, USA,
Ye Zheng, Steven Z. Josefowicz, Arnold Kas, Tin-Tin Chu, Marc A. Gavin & Alexander Y. Rudensky
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- Ye Zheng
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Correspondence toAlexander Y. Rudensky.
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Zheng, Y., Josefowicz, S., Kas, A. et al. Genome-wide analysis of Foxp3 target genes in developing and mature regulatory T cells.Nature 445, 936–940 (2007). https://doi.org/10.1038/nature05563
- Received: 30 October 2006
- Accepted: 21 December 2006
- Published: 21 January 2007
- Issue Date: 22 February 2007
- DOI: https://doi.org/10.1038/nature05563