Analysis of the role of Purα in the pathogenesis of Alzheimer's disease based on RNA-seq and ChIP-seq

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作者
Xiaoguang Shi
Shuanglai Ren
Bingying Zhang
Shanshan Guo
Wenxin He
Chengmin Yuan
Xiaofan Yang
Kevin Ig-lzevbekhai
Tao Sun
Qinwen Wang
Jianqi Cui
机构
[1] Ningxia Medical University,Ningxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of the National Key Laboratory
[2] Ningbo University,Zhejiang Provincial Key Laboratory of Pathophysiology, School of Medicine
[3] Hongqi Hospital Affiliated to Mudanjiang Medical University,Department of Neurology
[4] University of Pennsylvania,Perelman School of Medicine
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Scientific Reports | / 11卷
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摘要
Purine rich element binding protein A (Purα), encoded by the Purα gene, is an important transcriptional regulator that binds to DNA and RNA and is involved in processes such as DNA replication and RNA translation. Purα also plays an important role in the nervous system. To identify the function of Pura, we performed RNA sequence (RNA-seq) analysis of Purɑ-KO mouse hippocampal neuron cell line (HT22) to analyze the effect of Purα deletion on neuronal expression profiles. And combined with ChIP-seq analysis to explore the mechanism of Purα on gene regulation. In the end, totaly 656 differentially expressed genes between HT22 and Purα-KO HT22 cells have been found, which include 7 Alzheimer’s disease (AD)-related genes and 5 Aβ clearance related genes. 47 genes were regulated by Purα directly, the evidence based on CHIP-seq, which include Insr, Mapt, Vldlr, Jag1, etc. Our study provides the important informations of Purα in neuro-development. The possible regulative effects of Purα on AD-related genes consist inthe direct and indirect pathways of Purα in the pathogenesis of AD.
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