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C11orf95-RELA 重编程幕上室管膜瘤的 3D 表观基因组。

C11orf95-RELA reprograms 3D epigenome in supratentorial ependymoma.

机构信息

The Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.

Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX, USA.

出版信息

Acta Neuropathol. 2020 Dec;140(6):951-960. doi: 10.1007/s00401-020-02225-8. Epub 2020 Sep 9.

Abstract

Supratentorial ependymoma (ST-EPN) is a type of malignant brain tumor mainly seen in children. Since 2014, it has been known that an intrachromosomal fusion C11orf95-RELA is an oncogenic driver in ST-EPN [Parker et al. Nature 506:451-455 (2014); Pietsch et al. Acta Neuropathol 127:609-611 (2014)] but the molecular mechanisms of oncogenesis are unclear. Here we show that the C11orf95 component of the fusion protein dictates DNA binding activity while the RELA component is required for driving the expression of ependymoma-associated genes. Epigenomic characterizations using ChIP-seq and HiChIP approaches reveal that C11orf95-RELA modulates chromatin states and mediates chromatin interactions, leading to transcriptional reprogramming in ependymoma cells. Our findings provide important characterization of the molecular underpinning of C11orf95-RELA fusion and shed light on potential therapeutic targets for C11orf95-RELA subtype ependymoma.

摘要

幕上室管膜瘤(ST-EPN)是一种主要见于儿童的恶性脑肿瘤。自 2014 年以来,人们已经知道,染色体内融合 C11orf95-RELA 是 ST-EPN 的致癌驱动因素[Parker 等人,《自然》506:451-455(2014);Pietsch 等人,《神经病理学学报》127:609-611(2014)],但致癌的分子机制尚不清楚。在这里,我们表明融合蛋白的 C11orf95 成分决定了 DNA 结合活性,而 RELA 成分则是驱动室管膜瘤相关基因表达所必需的。使用 ChIP-seq 和 HiChIP 方法进行的表观基因组特征分析表明,C11orf95-RELA 调节染色质状态并介导染色质相互作用,导致室管膜瘤细胞中的转录重编程。我们的研究结果为 C11orf95-RELA 融合的分子基础提供了重要的特征描述,并为 C11orf95-RELA 亚型室管膜瘤的潜在治疗靶点提供了启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de6b/7666583/4f05c9629cd0/401_2020_2225_Fig1_HTML.jpg

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