Frye Richard E, Rose Shannon, McCullough Sandra, Bennuri Sirish C, Porter-Gill Patricia A, Dweep Harsh, Gill Pritmohinder S
Barrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ 85016, USA.
Department of Child Health, University of Arizona College of Medicine, Phoenix, AZ 85004, USA.
J Pers Med. 2021 Sep 17;11(9):922. doi: 10.3390/jpm11090922.
MicroRNAs (miRNAs) are important regulators of molecular pathways in psychiatric disease. Here, we examine differential miRNAs expression in lymphoblastoid cell lines (LCLs) derived from 10 individuals with autism spectrum disorder (ASD) and compare them to seven typically developing unrelated age- and gender-matched controls and 10 typically developing siblings. Small RNAseq analysis identified miRNAs, and selected miRNAs were validated using quantitative real-time polymerase reaction (qRT-PCR). KEGG analysis identified target pathways, and selected predicted mRNAs were validated using qRT-PCR.
Small RNAseq analysis identified that multiple miRNAs differentiated ASD from unrelated controls and ASD from typically developing siblings, with only one, hsa-miR-451a_R-1, being in common. Verification with qRT-PCR showed that miR-320a differentiated ASD from both sibling and unrelated controls and that several members of the miR-181 family differentiated ASD from unrelated controls. Differential expression of AKT2, AKT3, TNF α and CamKinase II predicted by KEGG analysis was verified by qRT-PCR. Expression of CamKinase II βwas found to be correlated with the severity of stereotyped behavior of the ASD participants.
This study provides insight into the mechanisms regulating molecular pathways in individuals with ASD and identifies differentiated regulated genes involved in both the central nervous system and the immune system.
微小RNA(miRNA)是精神疾病分子通路的重要调节因子。在此,我们检测了来自10名自闭症谱系障碍(ASD)个体的淋巴母细胞系(LCL)中miRNA的差异表达,并将其与7名年龄和性别匹配的发育正常的无关对照以及10名发育正常的同胞进行比较。小RNA测序分析鉴定出miRNA,所选miRNA通过定量实时聚合酶链反应(qRT-PCR)进行验证。KEGG分析确定了靶通路,所选预测的mRNA通过qRT-PCR进行验证。
小RNA测序分析表明,多个miRNA可区分ASD与无关对照以及ASD与发育正常的同胞,只有一个(hsa-miR-451a_R-1)是共有的。qRT-PCR验证显示,miR-320a可区分ASD与同胞及无关对照,miR-181家族的几个成员可区分ASD与无关对照。KEGG分析预测的AKT2、AKT3、TNFα和钙调蛋白激酶II的差异表达通过qRT-PCR得到验证。发现钙调蛋白激酶IIβ的表达与ASD参与者刻板行为的严重程度相关。
本研究深入了解了ASD个体分子通路的调节机制,并鉴定出参与中枢神经系统和免疫系统的差异调节基因。