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加权基因共表达网络分析(WGCNA)鉴定出与多囊卵巢综合征相关的环状RNA,这些环状RNA与RNA结合蛋白相互作用并作为微小RNA(miRNA)的海绵。

WGCNA Analysis Identifies Polycystic Ovary Syndrome-Associated Circular RNAs That Interact with RNA-Binding Proteins and Sponge miRNAs.

作者信息

Li Mengxiong, Zeng Zhi, Zhang Aiqing, Ye Qingjian, Su Shujun, Xia Tingting

机构信息

Department of Obstetrics and Gynecology, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, Guangdong, 518107, People's Republic of China.

The Department of Reproductive Medicine Center, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, 510000, People's Republic of China.

出版信息

Int J Gen Med. 2021 Nov 23;14:8737-8751. doi: 10.2147/IJGM.S335108. eCollection 2021.

Abstract

OBJECTIVE

Dysfunction of cumulus granulosa cells has been suggested as a contributor to abnormal folliculogenesis and the development of polycystic ovary syndrome (PCOS), but the underlying molecular mechanisms remain unclear. Recent studies indicate that circular RNAs (circRNAs) exert important roles for diseases. We aimed to screen crucial circRNAs of PCOS patients and predict their functions.

METHODS

The high-throughput datasets of circRNAs (GSE145296), microRNAs (miRNAs; GSE72274) and messenger RNAs (mRNAs; GSE155489) in cumulus cells of PCOS patients and controls were collected from the Gene Expression Omnibus database. Differentially expressed circRNAs (DECs), miRNAs (DEMs) and protein-coding genes (DEGs) were identified by the limma method. The weighted correlation network analysis (WGCNA) was conducted using the DECs to mine PCOS-associated modules. Hub DECs in modules were defined as both of |gene significance| and |module membership| >0.8. The downstream effectors of hub DECs were predicted by constructing DEC-DEM-DEG ceRNA and DEC-RNA binding protein (RBP) networks. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were performed to explore the functions of circRNAs.

RESULTS

A total of 3614 DECs, 3544 DEGs and 1469 DEMs were identified between PCOS and controls. WGCNA analysis yielded five PCOS-related modules, of which 190 DECs were hub circRNAs. Seventeen hub DECs, nine DEMs, and 315 DEGs were identified to construct the ceRNA network, while 56 hub DECs and two DEGs (MBNL2, RBPMS) constituted the circRNA-RBP network. Five hub DECs (hsa_circ_0063309, hsa_circ_0054275, hsa_circ_0056196, hsa_circ_0018108 and hsa_circ_0070987) were overlapped between ceRNA and DEC-MBNL2 regulatory networks and thus they may be pivotal for PCOS. Furthermore, hsa_circ_0099109 could interact with the RBP gene RBPMS. Function analyses showed these circRNAs were inflammation-, apoptosis- or steroidogenesis-related.

CONCLUSION

Aberrant expression of six circRNAs that function as RBP regulators or miRNA sponges may be possible mechanisms underlying the pathogenesis of PCOS by affecting apoptosis and steroidogenesis in cumulus cells.

摘要

目的

有研究提示卵丘颗粒细胞功能障碍是异常卵泡生成和多囊卵巢综合征(PCOS)发生发展的一个因素,但潜在分子机制仍不清楚。近期研究表明,环状RNA(circRNA)在疾病中发挥重要作用。我们旨在筛选PCOS患者关键的circRNA并预测其功能。

方法

从基因表达综合数据库收集PCOS患者和对照者卵丘细胞中circRNA(GSE145296)、微小RNA(miRNA;GSE72274)和信使RNA(mRNA;GSE155489)的高通量数据集。采用limma方法鉴定差异表达的circRNA(DEC)、miRNA(DEM)和蛋白质编码基因(DEG)。使用DEC进行加权基因共表达网络分析(WGCNA)以挖掘PCOS相关模块。模块中的枢纽DEC定义为|基因显著性|和|模块成员关系|均>0.8。通过构建DEC-DEM-DEG竞争性内源RNA(ceRNA)网络和DEC-RNA结合蛋白(RBP)网络预测枢纽DEC的下游效应分子。进行基因本体论和京都基因与基因组百科全书富集分析以探索circRNA的功能。

结果

在PCOS患者和对照者之间共鉴定出3614个DEC、3544个DEG和1469个DEM。WGCNA分析产生了5个PCOS相关模块,其中190个DEC为枢纽circRNA。鉴定出17个枢纽DEC、9个DEM和315个DEG构建ceRNA网络,而56个枢纽DEC和2个DEG(MBNL2、RBPMS)构成circRNA-RBP网络。5个枢纽DEC(hsa_circ_0063309、hsa_circ_00542�5、hsa_circ_0056196、hsa_circ_0018108和hsa_circ_0070987)在ceRNA和DEC-MBNL2调控网络之间重叠,因此它们可能对PCOS至关重要。此外,hsa_circ_0099109可与RBP基因RBPMS相互作用。功能分析表明这些circRNA与炎症、凋亡或类固醇生成相关。

结论

6个作为RBP调节因子或miRNA海绵发挥作用的circRNA异常表达可能是通过影响卵丘细胞凋亡和类固醇生成而成为PCOS发病机制的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa52/8627285/939991d20f0e/IJGM-14-8737-g0001.jpg

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