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Circular RNA expression profile and its potential regulative role in human abdominal aortic aneurysm

机译:圆形RNA表达谱及其在人腹主动脉瘤中的潜在调节作用

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This study aimed to identify the differentially expressed circular RNAs (circRNAs) between human abdominal aortic aneurysm (AAA) and the?control group. High-throughput sequencing was applied to determine the circRNA expression profiles of 4 paired aortic samples. Real-time quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was carried out to testify 6 randomly selected dysregulated circRNAs. Kyoto Encyclopedia of Genes and Genomes and Gene ontology (GO) analysis were conducted for functional annotation of the?parental genes. Additionally, interaction networks between circRNA and 5 putative microRNA (miRNA) partners were constructed. Finally, 411 differentially expressed circRNAs were discovered, including 266 downregulated and 145 upregulated circRNAs. Compared with the control group, the expression level of hsa (Homo sapiens) _circ_0005360 (LDLR) and hsa_circ_0002168 (TMEM189) were proved significantly lower in the AAA group by qRT-PCR. Regarding upregulated circRNAs, the most enriched GO molecular function, biological process and cellular component terms were poly(A) RNA binding, negative regulation of transcription from RNA polymerase II promoter and nucleoplasm, respectively. Moreover, circRNA/miRNA interaction networks showed that hsa_circ_0005360/miR-181b and hsa_circ_0002168/miR-15a axis might have a regulative role in human AAA. This study revealed new circRNAs potentially related to the pathogenesis of AAA. Further experimental studies are warranted to clarify the potential molecular mechanisms.
机译:该研究旨在鉴定人腹主动脉瘤(AAA)和α对照组之间的差异表达圆形RNA(Circrnas)。施用高通量测序以确定4个成对主动脉样品的CircRNA表达谱。进行实时定量逆转录 - 聚合酶链反应(QRT-PCR),以证明6种随机选择的脱少管CircrNA。进行基因和基因组和基因本体论(GO)分析的京都百科全书用于蛋白生物基因的功能注释。另外,构建了CircrNA和5个推定的MicroRNA(miRNA)合作伙伴之间的相互作用网络。最后,发现了411个差异表达的CircrNA,包括下调和145个上调Circrnas。与对照组相比,通过QRT-PCR在AAA组中显着降低了HSA(HOMO SAPIENS)_CIRC_0005360(LDLR)和HSA_CIRC_0002168(TMEM189)的表达水平。关于上调的CircrNA,最富集的GO分子功能,生物学过程和细胞组分术语分别是来自RNA聚合酶II启动子和核状的转录的多(a)RNA结合,负调节。此外,CircRNA / miRNA相互作用网络表明,HSA_CIRC_0005360 / miR-181b和hsa_circ_0002168 / mir-15a轴在人aaa中可能具有调节作用。本研究揭示了与AAA发病机制有关的新柳枝。有必要进一步的实验研究来阐明潜在的分子机制。

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