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大鼠周围神经损伤前后许旺细胞中 DNA 甲基化的比较。

Comparison of DNA Methylation in Schwann Cells before and after Peripheral Nerve Injury in Rats.

机构信息

Department of Orthopedics, Tianjin Medical University General Hospital, Tianjin, China.

Tianjin Neurological Institute, Key Laboratory of Post-Neuroinjury Neuro-Repair and Regeneration in Central Nervous System, Ministry of Education and Tianjin City, Tianjin, China.

出版信息

Biomed Res Int. 2017;2017:5393268. doi: 10.1155/2017/5393268. Epub 2017 Mar 26.

Abstract

This study aims to find the difference of genomewide DNA methylation in Schwann cells (SCs) before and after peripheral nerve system (PNS) injury by Methylated DNA Immunoprecipitation Sequencing (MeDIP-Seq) and seek meaningful differentially methylated genes related to repairment of injured PNS. SCs harvested from sciatic nerve were named as activated Schwann cells (ASCs), and the ones harvested from brachial plexus were named as normal Schwann cells (NSCs). Genomic DNA of ASCs and NSCs were isolated and MeDIP-Seq was conducted. Differentially methylated genes and regions were discovered and analyzed by bioinformatic methods. MeDIP-Seq analysis showed methylation differences were identified between ASCs and NSCs. The distribution of differentially methylated regions (DMRs) peaks in different components of genome was mainly located in distal intergenic regions. GO and KEGG analysis of these methylated genes were also conducted. The expression patterns of hypermethylated genes (Dgcr8, Zeb2, Dixdc1, Sox2, and Shh) and hypomethylated genes (Gpr126, Birc2) detected by qRT-PCR were opposite to the MeDIP analysis data with significance ( < 0.05), which proved MeDIP analysis data were real and believable. Our data serve as a basis for understanding the injury-induced epigenetic changes in SCs and the foundation for further studies on repair of PNS injury.

摘要

本研究旨在通过甲基化 DNA 免疫沉淀测序(MeDIP-Seq)寻找周围神经系统(PNS)损伤前后雪旺细胞(SCs)全基因组 DNA 甲基化的差异,并寻找与损伤 PNS 修复相关的有意义的差异甲基化基因。从坐骨神经中分离的 SCs 被命名为激活雪旺细胞(ASCs),从臂丛中分离的 SCs 被命名为正常雪旺细胞(NSCs)。分离 ASCs 和 NSCs 的基因组 DNA 并进行 MeDIP-Seq。通过生物信息学方法发现和分析差异甲基化基因和区域。MeDIP-Seq 分析表明,ASCs 和 NSCs 之间存在甲基化差异。差异甲基化区域(DMRs)峰在基因组不同成分中的分布主要位于远端基因间区域。对这些甲基化基因进行 GO 和 KEGG 分析。qRT-PCR 检测到的高甲基化基因(Dgcr8、Zeb2、Dixdc1、Sox2 和 Shh)和低甲基化基因(Gpr126、Birc2)的表达模式与 MeDIP 分析数据相反,具有统计学意义(<0.05),这证明了 MeDIP 分析数据是真实可信的。我们的数据为了解 SC 损伤诱导的表观遗传变化以及进一步研究 PNS 损伤修复提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4130/5385226/671703b67d18/BMRI2017-5393268.001.jpg

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