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首页> 外文期刊>Journal of cellular and molecular medicine. >Regulatory network of two circRNAs and an miRNA with their targeted genes under astilbin treatment in pulmonary fibrosis
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Regulatory network of two circRNAs and an miRNA with their targeted genes under astilbin treatment in pulmonary fibrosis

机译:ASTLP治疗肺纤维化中的两个circRNA和一个miRNA及其靶基因的调控网络

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Circular RNAs (circRNAs) are becoming new therapeutic drug targets. However, their profiles under astilbin treatment have not been reported yet. In this study, we analysed the global reprogramming of circRNA transcriptome and a regulatory network of circRNAs with their targeted genes under astilbin treatment in pulmonary fibrosis. A total of 145 circRNAs were differentially expressed in the astilbin‐treated group compared with the bleomycin‐treated group using RNA sequencing. In the bleomycin‐ and astilbin‐treated groups, 29 coexpressed circRNAs were found. The maximum number of circRNAs was distributed on chromosome two, and their length varieties were mainly within 1000?bp. Four differentially expressed circRNAs (circRNA‐662, 949, 394 and 986) were tested to validate the RNA sequencing data, and their targeted microRNAs and genes were analysed by qRT‐PCR, Western blot, Pearson correlation coefficient, a dual‐luciferase reporter system and anti‐AGOsub2/sub RNA immunoprecipitation. The results showed that circRNA‐662 and 949 can act as “miR‐29b sponges” targeting Gli2 and STAT3 to exert their functions. Our work suggests that the transcriptome complexity at the circRNA level under astilbin treatment. These circRNAs may be potential molecular targets for drug action.
机译:环状RNA(circRNA)成为新的治疗药物靶标。然而,尚未报道其在新霉素处理下的概况。在这项研究中,我们分析了在肺纤维化中在曲霉菌素处理下circRNA转录组的全球重编程和circRNA及其靶基因的调控网络。与使用博来霉素治疗的组相比,使用RNA测序的阿司匹林治疗组中总共有145个circRNA差异表达。在博来霉素和曲霉菌素治疗组中,发现了29个共表达的circRNA。 circRNA的最大数量分布在2号染色体上,其长度变异主要在1000?bp以内。测试了四个差异表达的circRNA(circRNA‐662、949、394和986)以验证RNA测序数据,并通过qRT-PCR,Western印迹,Pearson相关系数,双荧光素酶报告系统分析了其靶向的microRNA和基因。和抗AGO 2 RNA免疫沉淀。结果表明,circRNA-662和949可以充当靶向Gli2和STAT3的“ miR-29b海绵”,发挥其功能。我们的工作表明,在枯草杆菌蛋白酶处理下,circRNA水平的转录组复杂性。这些circRNAs可能是药物作用的潜在分子靶标。

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