The Ligase PIAS1 Restricts Natural Regulatory T Cell Differentiation by Epigenetic Repression

Author:

Liu Bin1,Tahk Samuel1,Yee Kathleen M.2,Fan Guoping3,Shuai Ke12

Affiliation:

1. Division of Hematology-Oncology, Department of Medicine, 11-934 Factor Building, 10833 Le Conte Avenue, University of California, Los Angeles, Los Angeles, CA 90095, USA.

2. Department of Biological Chemistry, University of California, Los Angeles, Los Angeles, CA 90095, USA.

3. Department of Human Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.

Abstract

PIAS1 Repression Regulatory T cells (T regs ) promote immune tolerance and protect against autoimmunity. T regs develop in the thymus, and their differentiation and acquisition of suppressive function requires expression of the transcription factor Foxp3. Although several transcription factors have been identified that turn on Foxp3 gene expression, how Foxp3 remains turned off in non-T regs is not well understood. Liu et al. (p. 521 ) have demonstrated that a regulator of cytokine signaling, PIAS1, represses Foxp3 expression by chromatin modification. PIAS1 promoted the methylation of the Foxp3 promoter by recruiting methyltransferases to inhibit expression. PIAS-deficient mice have more T reg cells than controls, and they appear to be protected against the development of experimental autoimmune encephalomyelitis, a mouse model for multiple sclerosis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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