首页> 外文期刊>Journal of Molecular Biology >Recruitment of Histone Methyltransferase Ehmt1 to Foxp3 TSDR Counteracts Differentiation of Induced Regulatory T Cells
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Recruitment of Histone Methyltransferase Ehmt1 to Foxp3 TSDR Counteracts Differentiation of Induced Regulatory T Cells

机译:组蛋白甲基转移酶EHMT1至FoxP3 TSDR的募集抵消了诱导的调节性T细胞的分化

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摘要

Differentiation toward CD4(+) regulatory T (Treg) cells is essentially dependent on an epigenetic program at Treg signature genes, which involves remodeling of the Treg-specific demethylated regions (TSDRs). In particular, the epigenetic status of the conserved non-coding sequence 2 of Foxp3 (Foxp3 TSDR) determines expression stability of the master transcription factor and thus Treg lineage identity. However, the molecular mechanisms controlling the epigenetic remodeling at TSDRs in Treg and conventional T cells are largely unknown.
机译:对CD4(+)调节性T(Treg)细胞的分化基本上依赖于Treg标志性基因的表观遗传程序,其涉及重新于特异性去甲基化区域(TSDR)的重塑。 特别地,Foxp3(FoxP3 TSDR)的保守非编码序列2的表观遗传状态决定了母转录因子的表达稳定性,从而确定了Treg谱系身份。 然而,在Treg和常规T细胞中控制TSDRS的表观遗传重塑的分子机制在很大程度上是未知的。

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