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首页> 外文期刊>Reproductive sciences >Expression Profiling of lncRNAs, miRNAs, and mRNAs and Their Differential Expression in Leiomyoma Using Next-Generation RNA Sequencing
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Expression Profiling of lncRNAs, miRNAs, and mRNAs and Their Differential Expression in Leiomyoma Using Next-Generation RNA Sequencing

机译:利用下一代RNA测序,LNCRNA,miRNA和MRNA的表达分析及其在平滑肌瘤中的差异表达

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摘要

The objective of this study was to identify the expression profile of long noncoding RNAs (lncRNAs) with concurrent assessment of microRNA (miRNA) and messenger RNA (mRNA) profiles in leiomyomas and paired myometrium using next-generation RNA sequencing and assembly of RNA transcripts. Total RNA was isolated from leiomyoma and paired myometrium (N = 8) and samples from 3 pairs were subjected to RNA sequencing. Normalized assembly of over 48 000 lncRNAs resulted in identification of 45 936 lncRNAs. Of these lncRNAs, 22 148 representing overlapping, intergenic, intronic, and antisense subtypes were expressed in all paired tissues, with 5941 (2813 up- and 3128 downregulated at 1.5 fold) differentially expressed in leiomyomas. Concurrent RNA sequencing revealed the expression of 2588 miRNAs and 21 814 mRNAs, of which 392 miRNAs and 16 559 mRNAs were expressed in all paired tissues. Of these transcripts, 56 and 92 miRNAs and 2030 and 1825 mRNAs were up- or downregulated at 1.5 fold, respectively, in leiomyoma as compared to myometrium. Using quantitative reverse transcription-polymerase chain reaction (QRT-PCR), we confirmed the expression of hepatocellular carcinoma upregulated (HULC), lnc-maternally expressed 3 (MEG3), long intergenic ncRNA 890 (LINC00890), TSIX, long intergenic ncRNA 473 (LINC00473), lnc-KLF9-1, and lnc-POTEM-3 (lncRNA-ATB) in leiomyoma and matched myometrium (N = 8). Collectively, the results presented here provide a comprehensive expression profile of lncRNAs in leiomyomas with concurrent integrated expression of miRNAs and mRNAs and implicate potential regulatory functions of lncRNAs through interactions with specific miRNAs and mRNAs which are known to be critical in the pathogenesis of leiomyoma.
机译:本研究的目的是鉴定长度非编码RNA(LNCRNA)的表达谱,并使用下一代RNA测序和RNA转录物组装成对的MICRORNA(miRNA)和信使RNA(mRNA)谱的同时评估MICRORNA(miRNA)和信使RNA(mRNA)谱。从平滑肌瘤中分离总RNA,并对3对的配对肌肌(n = 8)和样品进行RNA测序。标准化组装超过48 000LNCRNA,导致鉴定为45 936毫克。在所有配对组织中表达了这些LNCRNA,22148,代表重叠,代表性,内肠和反义亚型,用5941(在1.5倍下下调的3128和3128)在平滑肌瘤中差异表达。并发RNA测序显示2588 miRNA和21814 mRNA的表达,其中392 miRNA和1659mRNA在所有配对组织中表达。与肌瘤相比,这些转录物,56和92 miRNA和2030和1825mRNA分别在平滑肌瘤中升高或下调。使用定量逆转录 - 聚合酶链反应(QRT-PCR),我们证实了肝细胞癌上调的表达(Hulc),LNC-母体表达3(Meg3),长的基因NcRNA 890(LINC00890),Tsix,长的NcRNA 473( LINC00473),LNC-KLF9-1和LNC-Potem-3(LNC-Potem-3(LNCRNA-ATB)在平滑肌瘤和匹配的肌瘤中(n = 8)。总的来说,本文呈现的结果在平滑肌瘤中具有综合表达谱,其具有miRNA和MRNA的并发整合表达,并通过与特定miRNA和MRNA的相互作用来暗示LNCRNA的潜在调节功能,这些功能在平滑肌瘤的发病机制中至关重要。

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