Huang Sai, Feng Cong, Chen Li, Huang Zhi, Zhou Xuan, Li Bei, Wang Li-Li, Chen Wei, Lv Fa-Qin, Li Tan-Shi
Department of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).
Department of Emergency, General Hospital of the PLA, Beijing, China (mainland).
Med Sci Monit. 2016 Sep 24;22:3394-3408. doi: 10.12659/msm.900783.
BACKGROUND This study aimed to identify the potential key long non-coding RNAs (lncRNAs) and target genes associated with pneumonia using lncRNA sequencing (lncRNA-seq). MATERIAL AND METHODS A total of 9 peripheral blood samples from patients with mild pneumonia (n=3) and severe pneumonia (n=3), as well as volunteers without pneumonia (n=3), were received for lncRNA-seq. Based on the sequencing data, differentially expressed lncRNAs (DE-lncRNAs) were identified by the limma package. After the functional enrichment analysis, target genes of DE-lncRNAs were predicted, and the regulatory network was constructed. RESULTS In total, 99 DE-lncRNAs (14 upregulated and 85 downregulated ones) were identified in the mild pneumonia group and 85 (72 upregulated and 13 downregulated ones) in the severe pneumonia group, compared with the control group. Among these DE-lncRNAs, 9 lncRNAs were upregulated in both the mild and severe pneumonia groups. A set of 868 genes were predicted to be targeted by these 9 DE-lncRNAs. In the network, RP11-248E9.5 and RP11-456D7.1 targeted the majority of genes. RP11-248E9.5 regulated several genes together with CTD-2300H10.2, such as QRFP and EPS8. Both upregulated RP11-456D7.1 and RP11-96C23.9 regulated several genes, such as PDK2. RP11-456D7.1 also positively regulated CCL21. CONCLUSIONS These novel lncRNAs and their target genes may be closely associated with the progression of pneumonia.
背景 本研究旨在通过长链非编码RNA测序(lncRNA-seq)鉴定与肺炎相关的潜在关键长链非编码RNA(lncRNA)和靶基因。
材料与方法 共收集了9份外周血样本,其中包括轻度肺炎患者(n = 3)、重度肺炎患者(n = 3)以及无肺炎志愿者(n = 3)的样本,用于lncRNA-seq检测。基于测序数据,使用limma软件包鉴定差异表达的lncRNA(DE-lncRNA)。经过功能富集分析后,预测DE-lncRNA的靶基因,并构建调控网络。
结果 与对照组相比,轻度肺炎组共鉴定出99个DE-lncRNA(14个上调,85个下调),重度肺炎组鉴定出85个(72个上调,13个下调)。在这些DE-lncRNA中,有9个lncRNA在轻度和重度肺炎组中均上调。预测这9个DE-lncRNA靶向一组868个基因。在该网络中,RP11-248E9.5和RP11-456D7.1靶向的基因最多。RP11-248E9.5与CTD-2300H10.2共同调控多个基因,如QRFP和EPS8。上调的RP11-456D7.1和RP11-96C23.9均调控多个基因,如PDK2。RP11-456D7.1还正向调控CCL21。
结论 这些新的lncRNA及其靶基因可能与肺炎的进展密切相关。