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表征自闭症谱系障碍中的微小RNA编辑和突变位点。

Characterizing microRNA editing and mutation sites in Autism Spectrum Disorder.

作者信息

Wu Xingwang, Yang Huaide, Lin Han, Suo Angbaji, Wu Shuai, Xie Wenping, Zhou Nan, Guo Shiyong, Ding Hao, Zhou Guangchen, Qiu Zhichao, Shi Hong, Yang Jun, Zheng Yun

机构信息

State Key Laboratory of Primate Biomedical Research, Kunming University of Science and Technology, Kunming, Yunnan, China.

Institute of Primate Translational Medicine, Kunming University of Science and Technology, Kunming, Yunnan, China.

出版信息

Front Mol Neurosci. 2023 Jan 20;15:1105278. doi: 10.3389/fnmol.2022.1105278. eCollection 2022.

Abstract

Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder whose pathogenesis is still unclear. MicroRNAs (miRNAs) are a kind of endogenous small non-coding RNAs that play important roles in the post-transcriptional regulation of genes. Recent researches show that miRNAs are edited in multiple ways especially in central nervous systems. A-to-I editing of RNA catalyzed by Adenosine deaminases acting on RNA (ADARs) happens intensively in brain and is also noticed in other organs and tissues. Although miRNAs are widely edited in human brain, miRNA editing in ASD is still largely unexplored. In order to reveal the editing events of miRNAs in ASD, we analyzed 131 miRNA-seq samples from 8 different brain regions of ASD patients and normal controls. We identified 834 editing sites with significant editing levels, of which 70 sites showed significantly different editing levels in the superior frontal gyrus samples of ASD patients (ASD-SFG) when compared with those of control samples. The editing level of an A-to-I editing site in hsa-mir-376a-1 (hsa-mir-376a-1_9_A_g) in ASD-SFG is higher than that of normal controls, and the difference is exaggerated in individuals under 10 years. The increased expression of is consistent with the increased editing level of hsa-mir-376a-1_9_A_g in ASD-SFG samples compared to normal SFG samples. Furthermore, we verify that A-to-I edited hsa-mir-376a-5p directly represses and , which may contribute to the abnormal neuronal development of ASD patients. These results provide new insights into the mechanism of ASD.

摘要

自闭症谱系障碍(ASD)是一种神经发育障碍,其发病机制仍不清楚。微小RNA(miRNA)是一类内源性小非编码RNA,在基因的转录后调控中发挥重要作用。最近的研究表明,miRNA以多种方式进行编辑,尤其是在中枢神经系统中。由作用于RNA的腺苷脱氨酶(ADARs)催化的RNA的A到I编辑在大脑中大量发生,在其他器官和组织中也有发现。尽管miRNA在人类大脑中被广泛编辑,但ASD中的miRNA编辑仍在很大程度上未被探索。为了揭示ASD中miRNA的编辑事件,我们分析了来自ASD患者和正常对照的8个不同脑区的131个miRNA序列样本。我们鉴定出834个具有显著编辑水平的编辑位点,其中70个位点在ASD患者的额上回样本(ASD-SFG)中与对照样本相比显示出显著不同的编辑水平。ASD-SFG中hsa-mir-376a-1(hsa-mir-376a-1_9_A_g)的一个A到I编辑位点的编辑水平高于正常对照,且在10岁以下个体中差异更为明显。与正常SFG样本相比,ASD-SFG样本中 的表达增加与hsa-mir-376a-1_9_A_g的编辑水平增加一致。此外,我们验证了A到I编辑的hsa-mir-376a-5p直接抑制 和 ,这可能导致ASD患者神经元发育异常。这些结果为ASD的发病机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2559/9895120/df35608b03e4/fnmol-15-1105278-g0001.jpg

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