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首页> 外文期刊>Journal of Molecular Biology >The Third Intron of IRF8 Is a Cell-Type-Specific Chromatin Priming Element during Mouse Embryonal Stem Cell Differentiation
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The Third Intron of IRF8 Is a Cell-Type-Specific Chromatin Priming Element during Mouse Embryonal Stem Cell Differentiation

机译:IRF8的第三内含子是小鼠胚胎干细胞分化期间的细胞型特异性染色质灌注元件

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摘要

Interferon regulatory factor 8 (IRF8) is a nuclear transcription factor that plays a key role in the hierarchical differentiation of hematopoietic stem cells toward monocyte/dendritic cell lineages. Therefore, its expression is mainly limited to bone marrow-derived cells. The molecular mechanisms governing this cell-type-restricted expression have been described. However, the molecular mechanisms that are responsible for its silencing in non-hematopoietic cells are elusive. Recently, we demonstrated a role for IRF8 third intron in restricting its expression in non-hematopoietic cells. Furthermore, we showed that this intron alone is sufficient to promote repressed chromatin a cell-type-specific manner. Here we demonstrate the effect of the IRF8 third intron on chromatin conformation during murine embryonal stem cell differentiation. Using genome editing, we provide data showing that the third intron plays a key role in priming the chromatin state of the IRF8 locus during cell differentiation. It mediates dual regulatory effects in a cell-type-specific mode. It acts as a repressor element governing chromatin state of the IRF8 locus during embryonal stem cell differentiation to cardiomyocytes that are expression-restrictive cells. Conversely, it functions as an activator element that is essential for open chromatin structure during the differentiation of these cells to dendritic cells that are expression-permissive cells. Together, these results point to the role of IRF8 third intron as a cell-type-specific chromatin priming element during embryonal stem cell differentiation. These data add another layer to our understanding of the molecular mechanisms governing misexpression of a cell-type-specific gene such as IRF8. (C) 2018 Elsevier Ltd. All rights reserved.
机译:干扰素调节因子8(IRF8)是核转录因子,其在造血干细胞对单核细胞/树突细胞谱系中起着关键作用。因此,其表达主要限于骨髓衍生细胞。已经描述了治疗该细胞类型限制表达的分子机制。然而,对其在非造血细胞中沉默的分子机制是难以捉摸的。最近,我们展示了IRF8第三内含子在限制非造血细胞中表达的作用。此外,我们表明,这种内含子足以促进抑制染色质目的细胞类型特异性的方式。在这里,我们证明了IRF8第三内含子对鼠胚胎干细胞分化期间的染色质构象的影响。使用基因组编辑,我们提供数据显示第三内含子在细胞分化期间在灌注IRF8基因座的染色质状态时发挥关键作用。它以特定于细胞类型的模式介导双重调节效果。它用作胚胎干细胞分化期间对IRF8基因座的染色质染色质的阻遏物元素,其与表现限制细胞的心肌细胞。相反,它用作活化剂元件,该活化剂元素对于在这些细胞与表达允许细胞的树突细胞的分化期间对于开放染色质结构是必不可少的。这些结果在胚胎干细胞分化期间指向IRF8第三内含子作为细胞型染色质灌注元素的作用。这些数据添加了另一种层,以了解用于治疗细胞类型特异性基因如IRF8的微调的分子机制。 (c)2018年elestvier有限公司保留所有权利。

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