Institute of Integrative Medicine, Department of Integrated Traditional Chinese and Western Medicine, Xiangya Hospital, Central South University, Changsha 410008, China.
Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Aging (Albany NY). 2020 Nov 16;12(22):22794-22813. doi: 10.18632/aging.103938.
Transfer-RNA-derived small RNAs (tsRNAs) are a novel class of short non-coding RNAs, that possess regulatory functions. However, their biological roles in hemorrhagic stroke are not understood. In this study, by RNA sequencing, we investigated the tsRNA expression profiles of intracerebral hemorrhagic rat brains in the chronic phase. A total of 331 tsRNAs were identified (308 in sham and 309 in intracerebral hemorrhage). Among them, the validation revealed that 7 tsRNAs (1 up-regulated and 6 down-regulated) were significantly changed. Subsequently, we predicted the target mRNAs of the 7 tsRNAs. Through integrative analysis, the predicted targets were validated by mRNA microarray data. Moreover, we confirmed the functions of tsRNAs targeting mRNAs . Furthermore, using bioinformatics tools and databases, we developed a tsRNA-mRNA-pathway interaction network to visualize their potential functions. Bioinformatics analyses and confirmatory experiments indicated that the altered genes were mainly enriched in several signaling pathways. These pathways were interrelated with intracerebral hemorrhage, such as response to oxidative stress, endocytosis, and regulation of G protein-coupled receptor signaling pathway. In summary, this study systematically revealed the profiles of tsRNAs after an experimental intracerebral hemorrhage. These results may provide novel therapeutic targets following a hemorrhagic stroke in the chronic phase.
转移 RNA 衍生的小 RNA(tsRNA)是一类新型的短非编码 RNA,具有调节功能。然而,它们在出血性中风中的生物学作用尚不清楚。在这项研究中,我们通过 RNA 测序研究了慢性期脑出血大鼠脑内的 tsRNA 表达谱。共鉴定出 331 种 tsRNA(假手术组 308 种,脑出血组 309 种)。其中,验证结果显示有 7 种 tsRNA(1 种上调,6 种下调)明显变化。随后,我们预测了 7 种 tsRNA 的靶 mRNA。通过综合分析,利用 mRNA 微阵列数据验证了预测的靶标。此外,我们还证实了靶向 mRNA 的 tsRNA 的功能。此外,我们利用生物信息学工具和数据库构建了 tsRNA-mRNA-通路相互作用网络,以可视化它们的潜在功能。生物信息学分析和验证实验表明,改变的基因主要富集在几个信号通路中。这些通路与脑出血相关,如氧化应激反应、内吞作用和 G 蛋白偶联受体信号通路的调节。总之,本研究系统地揭示了实验性脑出血后 tsRNA 的图谱。这些结果可能为脑出血慢性期提供新的治疗靶点。