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一个长链非编码 RNA 鉴定出树突状细胞分化负反馈调控中的增强子元件。

A lncRNA identifies enhancer element in negative feedback control of dendritic cell differentiation.

机构信息

Department of Cell Biology, Institute of Biomedical Engineering, RWTH Aachen University Medical School, Aachen, Germany.

Helmholtz Institute for Biomedical Engineering, RWTH Aachen University, Aachen, Germany.

出版信息

Elife. 2023 Mar 14;12:e83342. doi: 10.7554/eLife.83342.

Abstract

Transcription factors play a determining role in lineage commitment and cell differentiation. Interferon regulatory factor 8 (IRF8) is a lineage determining transcription factor in hematopoiesis and master regulator of dendritic cells (DC), an important immune cell for immunity and tolerance. IRF8 is prominently upregulated in DC development by autoactivation and controls both DC differentiation and function. However, it is unclear how autoactivation is controlled and eventually limited. Here, we identified a novel long non-coding RNA transcribed from the +32 kb enhancer downstream of transcription start site and expressed specifically in mouse plasmacytoid DC (pDC), referred to as . The locus interacts with the promoter and shows differential epigenetic signatures in pDC versus classical DC type 1 (cDC1). Interestingly, a sequence element of the promoter, but not itself, is crucial for mouse pDC and cDC1 differentiation, and this sequence element confers feedback inhibition of expression. Taken together, in DC development autoactivation is first initiated by flanking enhancers and then second controlled by feedback inhibition through the promoter element in the +32 kb enhancer. Our work reveals a previously unrecognized negative feedback loop of that orchestrates its own expression and thereby controls DC differentiation.

摘要

转录因子在谱系决定和细胞分化中起着决定性的作用。干扰素调节因子 8 (IRF8) 是造血中的谱系决定转录因子,也是树突状细胞 (DC) 的主要调节因子,DC 是免疫和耐受的重要免疫细胞。IRF8 通过自身激活在 DC 发育中显著上调,并控制 DC 的分化和功能。然而,自身激活是如何被控制和最终受到限制的尚不清楚。在这里,我们鉴定了一个新的长非编码 RNA,它从转录起始位点下游的 +32kb 增强子转录而来,并且特异性地在小鼠浆细胞样 DC (pDC) 中表达,称为 。 基因座与 启动子相互作用,在 pDC 与经典 DC 类型 1 (cDC1) 中表现出不同的表观遗传特征。有趣的是, 启动子的一个序列元件,但不是 本身,对于小鼠 pDC 和 cDC1 分化至关重要,并且这个序列元件赋予 表达的反馈抑制。总之,在 DC 发育过程中,侧翼增强子首先启动自身激活,然后通过 +32kb 增强子中的 启动子元件进行反馈抑制来控制自身激活。我们的工作揭示了一个以前未被识别的 负反馈回路,该回路协调其自身的表达,从而控制 DC 的分化。

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