
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.
CD4-Positive T-Lymphocytes, Male, Binding Sites, Encephalomyelitis, Autoimmune, Experimental, Lymphopoiesis, Forkhead Transcription Factors, Mice, Inbred Strains, DNA Methylation, Protein Inhibitors of Activated STAT, Chromatin, DNA Methyltransferase 3A, Epigenesis, Genetic, Histones, Mice, Inbred C57BL, Repressor Proteins, Mice, Animals, Female, DNA (Cytosine-5-)-Methyltransferases, Promoter Regions, Genetic
CD4-Positive T-Lymphocytes, Male, Binding Sites, Encephalomyelitis, Autoimmune, Experimental, Lymphopoiesis, Forkhead Transcription Factors, Mice, Inbred Strains, DNA Methylation, Protein Inhibitors of Activated STAT, Chromatin, DNA Methyltransferase 3A, Epigenesis, Genetic, Histones, Mice, Inbred C57BL, Repressor Proteins, Mice, Animals, Female, DNA (Cytosine-5-)-Methyltransferases, Promoter Regions, Genetic
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 99 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
