Genome-wide interrogation of transfer RNA-derived small RNAs in a mouse model of traumatic brain injury

被引:0
|
作者
Xiao-Jian Xu [1 ]
Meng-Shi Yang [1 ,2 ]
Bin Zhang [1 ,2 ]
Qian-Qian Ge [1 ,2 ]
Fei Niu [1 ]
Jin-Qian Dong [1 ,2 ]
Yuan Zhuang [1 ,2 ]
Bai-Yun Liu [1 ,2 ,3 ,4 ]
机构
[1] Beijing Key Laboratory of Central Nervous System Injury, Beijing Neurosurgical Institute, Capital Medical University
[2] Beijing Key Laboratory of Central Nervous System Injury and Department of Neurosurgery, Beijing Neurosurgical Institute and Beijing Tiantan Hospital, Capital Medical University
[3] Nerve Injury and Repair Center of Beijing Institute for Brain Disorders
[4] China National Clinical Research Center for Neurological Diseases
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
R651.15 []; R-332 [医用实验动物学];
学科分类号
1001 ; 1002 ; 100210 ;
摘要
Transfer RNA(t RNA)-derived small RNAs(ts RNAs) are a recently established family of regulatory small non-coding RNAs that modulate diverse biological processes. Growing evidence indicates that ts RNAs are involved in neurological disorders and play a role in the pathogenesis of neurodegenerative disease. However, whether ts RNAs are involved in traumatic brain injury-induced secondary injury remains poorly understood. In this study, a mouse controlled cortical impact model of traumatic brain injury was established, and integrated ts RNA and messenger RNA(m RNA) transcriptome sequencing were used. The results revealed that 103 ts RNAs were differentially expressed in the mouse model of traumatic brain injury at 72 hours, of which 56 ts RNAs were upregulated and 47 ts RNAs were downregulated. Based on micro RNA-like seed matching and Pearson correlation analysis, 57 differentially expressed ts RNA-m RNA interaction pairs were identified, including 29 ts RNAs and 26 m RNAs. Moreover, Gene Ontology annotation of target genes revealed that the significantly enriched terms were primarily associated with inflammation and synaptic function. Collectively, our findings suggest that ts RNAs may be associated with traumatic brain injury-induced secondary brain injury, and are thus a potential therapeutic target for traumatic brain injury. The study was approved by the Beijing Neurosurgical Institute Animal Care and Use Committee(approval No. 20190411) on April 11, 2019.
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页码:386 / 394
页数:9
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