Egr2 Promoter反义 RNA 在调节许旺细胞染色质景观中的作用

IF 3.9 3区 工程技术 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Margot Martinez Moreno, David Karambizi, Hyeyeon Hwang, Kristen Fregoso, Madison J Michles, Eduardo Fajardo, Andras Fiser, Nikos Tapinos
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引用次数: 0

摘要

背景:许旺细胞(SC)及其可塑性有助于外周神经系统在损伤后的神经再生能力。Egr2/Krox20 启动子反义 RNA(Egr2-AS)能在周围神经损伤后招募染色质重塑复合物抑制 Egr2 的转录。方法:RNA-seq 和 ATAC-seq:对对照细胞、Lenti-GFP转导细胞和过表达Egr2-AS(Lenti-AS)的细胞进行RNA-seq和ATAC-seq分析。将 Egr2 AS-RNA 克隆到 pLVX-DsRed-Express2-N1 慢病毒表达载体(Clontech, Mountain View, CA, USA)中,并测定 AS-RNA 的表达水平。从大鼠 SCs 中免疫沉淀 Ezh2 和 Wdr5,并针对 AS-Egr2 RNA 进行 RT-qPCR。使用 ChIP 和 DNA 纯化柱对相关启动子进行 qPCR。Hi-C、HiC-DC+、R、Bioconductor 和 TOBIAS 被用于显著和差异环路分析、COREs 和 CORE-promotor 环路的鉴定、启动子位点 TF 活性的比较以及位点特异性 TF 脚印的鉴定。OnTAD 用于检测 TADs,Juicer 用于鉴定 A/B 区。结果我们在这里发现,Neuregulin-ErbB2/3 信号轴介导 Egr2-AS 与 YY1Ser184 结合并调节其表达。Egr2-AS 可调节许旺细胞染色质的可及性,并与两种不同的组蛋白修饰复合物相互作用。它与 EZH2 和 WDR5 结合,使 H3K27me3 和 H3K4me3 分别靶向 Egr2 和 C-JUN 的启动子。Egr2-AS的表达会导致全局染色质景观的重组以及环路形成的定量变化和AP-1基因富集的结构域边界的接触频率。此外,Egr2-AS 还诱导了分级 TAD 的变化,并增加了超级增强子调控中枢与 mTOR 启动子之间的 TAD 间环的转录因子结合得分。结论我们的研究结果表明,Neuregulin-ErbB2/3-YY1调控Egr2-AS的表达,而Egr2-AS介导了许旺细胞染色质景观的重塑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of the Egr2 Promoter Antisense RNA in Modulating the Schwann Cell Chromatin Landscape.

Background: Schwann cells (SCs) and their plasticity contribute to the peripheral nervous system's capacity for nerve regeneration after injury. The Egr2/Krox20 promoter antisense RNA (Egr2-AS) recruits chromatin remodeling complexes to inhibit Egr2 transcription following peripheral nerve injury. Methods: RNA-seq and ATAC-seq were performed on control cells, Lenti-GFP-transduced cells, and cells overexpressing Egr2-AS (Lenti-AS). Egr2 AS-RNA was cloned into the pLVX-DsRed-Express2-N1 lentiviral expression vector (Clontech, Mountain View, CA, USA), and the levels of AS-RNA expression were determined. Ezh2 and Wdr5 were immunoprecipitated from rat SCs and RT-qPCR was performed against AS-Egr2 RNA. ChIP followed by DNA purification columns was used to perform qPCR for relevant promoters. Hi-C, HiC-DC+, R, Bioconductor, and TOBIAS were used for significant and differential loop analysis, identifications of COREs and CORE-promotor loops, comparisons of TF activity at promoter sites, and identification of site-specific TF footprints. OnTAD was used to detect TADs, and Juicer was used to identify A/B compartments. Results: Here we show that a Neuregulin-ErbB2/3 signaling axis mediates binding of the Egr2-AS to YY1Ser184 and regulates its expression. Egr2-AS modulates the chromatin accessibility of Schwann cells and interacts with two distinct histone modification complexes. It binds to EZH2 and WDR5 and enables targeting of H3K27me3 and H3K4me3 to promoters of Egr2 and C-JUN, respectively. Expression of the Egr2-AS results in reorganization of the global chromatin landscape and quantitative changes in the loop formation and contact frequency at domain boundaries exhibiting enrichment for AP-1 genes. In addition, the Egr2-AS induces changes in the hierarchical TADs and increases transcription factor binding scores on an inter-TAD loop between a super-enhancer regulatory hub and the promoter of mTOR. Conclusions: Our results show that Neuregulin-ErbB2/3-YY1 regulates the expression of Egr2-AS, which mediates remodeling of the chromatin landscape in Schwann cells.

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来源期刊
Biomedicines
Biomedicines Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.20
自引率
8.50%
发文量
2823
审稿时长
8 weeks
期刊介绍: Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.
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