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整合的微小RNA-信使核糖核酸表达谱分析鉴定出与自闭症相关的新靶点和网络。

Integrated microRNA-mRNA Expression Profiling Identifies Novel Targets and Networks Associated with Autism.

作者信息

Gill Pritmohinder S, Dweep Harsh, Rose Shannon, Wickramasinghe Priyankara J, Vyas Kanan K, McCullough Sandra, Porter-Gill Patricia A, Frye Richard E

机构信息

Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR 72202, USA.

Arkansas Children's Research Institute, Little Rock, AR 72202, USA.

出版信息

J Pers Med. 2022 Jun 1;12(6):920. doi: 10.3390/jpm12060920.

Abstract

Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder, with mutations in hundreds of genes contributing to its risk. Herein, we studied lymphoblastoid cell lines (LCLs) from children diagnosed with autistic disorder ( = 10) and controls ( = 7) using RNA and miRNA sequencing profiles. The sequencing analysis identified 1700 genes and 102 miRNAs differentially expressed between the ASD and control LCLs ( ≤ 0.05). The top upregulated genes were , , and , and the top upregulated miRNAs were , , and . The RT-qPCR analysis confirmed the sequencing results for randomly selected candidates: , , , and The functional enrichment analysis showed pathways involved in ASD control proliferation of neuronal cells, cell death of immune cells, epilepsy or neurodevelopmental disorders, WNT and PTEN signaling, apoptosis, and cancer. The integration of mRNA and miRNA sequencing profiles by miRWalk2.0 identified correlated changes in miRNAs and their targets' expression. The integration analysis found significantly dysregulated miRNA-gene pairs in ASD. Overall, these findings suggest that mRNA and miRNA expression profiles in ASD are greatly altered in LCLs and reveal numerous miRNA-gene interactions that regulate critical pathways involved in the proliferation of neuronal cells, cell death of immune cells, and neuronal development.

摘要

自闭症谱系障碍(ASD)是一种复杂的神经发育障碍,数百个基因的突变会增加其发病风险。在此,我们使用RNA和miRNA测序图谱研究了来自被诊断为自闭症障碍儿童(n = 10)和对照组(n = 7)的淋巴母细胞系(LCLs)。测序分析确定了ASD和对照LCLs之间差异表达的1700个基因和102个miRNA(p≤0.05)。上调程度最高的基因是 、 和 ,上调程度最高的miRNA是 、 和 。RT-qPCR分析证实了随机选择的候选基因的测序结果: 、 、 和 。功能富集分析显示ASD控制神经元细胞增殖、免疫细胞死亡、癫痫或神经发育障碍、WNT和PTEN信号传导、细胞凋亡以及癌症的相关途径。通过miRWalk2.0对mRNA和miRNA测序图谱进行整合,确定了miRNA及其靶标表达的相关变化。整合分析发现ASD中miRNA-基因对显著失调。总体而言,这些发现表明ASD中LCLs的mRNA和miRNA表达谱发生了很大改变,并揭示了众多调节神经元细胞增殖、免疫细胞死亡和神经元发育关键途径的miRNA-基因相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e32d/9225282/b502ef3abfec/jpm-12-00920-g001.jpg

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