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先天性小耳畸形中微小RNA综合调控网络的生物信息学分析

Bioinformatics analysis of microRNA comprehensive regulatory network in congenital microtia.

作者信息

Wei Gangqiang

机构信息

Burn and Plastic Surgery Department, Tangshan Gongren Hospital, Tangshan 063000, Hebei, China.

出版信息

Int J Pediatr Otorhinolaryngol. 2015 Oct;79(10):1727-31. doi: 10.1016/j.ijporl.2015.07.036. Epub 2015 Aug 4.

Abstract

PURPOSE

This study was aimed to reveal the involvement of miRNAs in the progression of microtia by bioinformatics analyses.

METHODS

The data in this study came from the paper of Li et al. who analyzed the microRNA (miRNA) expression profiling between congenital microtia and normal controls. Based on the 11 identified differentially expressed miRNAs, we predicted the target genes, long non-coding RNAs (lncRNA) and transcription factors (TFs). Then we constructed the miRNAs-centered comprehensive regulatory network. In addition, we performed functional enrichment analysis to analyze the functions of target genes.

RESULTS

From the miRNAs comprehensive regulatory network, we found that has-miR-203 regulated a large number of target genes and lncRNAs, including suppressor of cytokine signaling 3 (SOCS3) and metastasis associated in lung adenocarcinoma transcript 1 (MALAT1). The has-miR-185, has-miR-451 and has-miR-200c were regulated by a host of TFs including signal transducer and activator of transcription 1 (STAT1) and STAT2. Additionally, the target genes of hsa-miR-486-5p were mainly enriched in 17 Gene Ontology terms and target genes of has-miRNA-203 were enriched in 6 pathways.

CONCLUSIONS

The expression of has-miR-203, has-miR-200c and has-miR-451 were significantly different in microtia. Target gene of SOCS3, TFs of STAT1 and STAT2, and lncRNA of MALAT1 may play important roles in the development of the external ear.

摘要

目的

本研究旨在通过生物信息学分析揭示微小RNA(miRNA)在小耳畸形进展中的作用。

方法

本研究的数据来自Li等人的论文,他们分析了先天性小耳畸形与正常对照之间的微小RNA(miRNA)表达谱。基于11个鉴定出的差异表达miRNA,我们预测了靶基因、长链非编码RNA(lncRNA)和转录因子(TF)。然后构建了以miRNA为中心的综合调控网络。此外,我们进行了功能富集分析以分析靶基因的功能。

结果

从miRNA综合调控网络中,我们发现has-miR-203调控大量靶基因和lncRNA,包括细胞因子信号转导抑制因子3(SOCS3)和肺腺癌转移相关转录本1(MALAT1)。has-miR-185、has-miR-451和has-miR-200c受包括信号转导和转录激活因子1(STAT1)和STAT2在内的多种TF调控。此外,hsa-miR-486-5p的靶基因主要富集在17个基因本体学术语中,has-miRNA-203的靶基因富集在6条通路中。

结论

has-miR-203、has-miR-200c和has-miR-451在小耳畸形中的表达存在显著差异。SOCS3的靶基因、STAT1和STAT2的TF以及MALAT1的lncRNA可能在外耳发育中起重要作用。

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