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与自闭症谱系障碍及相关障碍相关的 microRNA 和 microRNA 靶标变异。

MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.

机构信息

Department of Genetics, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.

Department of Statistics, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.

出版信息

Genes (Basel). 2022 Jul 26;13(8):1329. doi: 10.3390/genes13081329.

DOI:10.3390/genes13081329
PMID:35893067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9329941/
Abstract

Autism spectrum disorder (ASD) is a childhood neurodevelopmental disorder with a complex and heterogeneous genetic etiology. MicroRNA (miRNA), a class of small non-coding RNAs, could regulate ASD risk genes post-transcriptionally and affect broad molecular pathways related to ASD and associated disorders. Using whole-genome sequencing, we analyzed 272 samples in 73 families in the New Jersey Language and Autism Genetics Study (NJLAGS) cohort. Families with at least one ASD patient were recruited and were further assessed for language impairment, reading impairment, and other associated phenotypes. A total of 5104 miRNA variants and 1,181,148 3' untranslated region (3' UTR) variants were identified in the dataset. After applying several filtering criteria, including population allele frequency, brain expression, miRNA functional regions, and inheritance patterns, we identified high-confidence variants in five brain-expressed miRNAs (targeting 326 genes) and 3' UTR miRNA target regions of 152 genes. Some genes, such as and , were identified in multiple families. Using Gene Ontology overrepresentation analysis and protein-protein interaction network analysis, we identified clusters of genes and pathways that are important for neurodevelopment. The miRNAs and miRNA target genes identified in this study are potentially involved in neurodevelopmental disorders and should be considered for further functional studies.

摘要

自闭症谱系障碍 (ASD) 是一种儿童神经发育障碍,具有复杂和异质的遗传病因。微小 RNA (miRNA) 是一类小的非编码 RNA,可以在转录后调节 ASD 风险基因,影响与 ASD 相关的广泛分子途径和相关疾病。我们使用全基因组测序,对新泽西语言和自闭症遗传学研究 (NJLAGS) 队列中的 73 个家庭的 272 个样本进行了分析。招募了至少有一名 ASD 患者的家庭,并进一步评估了语言障碍、阅读障碍和其他相关表型。在该数据集中共鉴定出 5104 个 miRNA 变体和 1181148 个 3'非翻译区 (3'UTR) 变体。应用包括群体等位基因频率、大脑表达、miRNA 功能区和遗传模式在内的几种过滤标准后,我们鉴定了 5 个在大脑中表达的 miRNA(靶向 326 个基因)和 152 个基因的 3'UTR miRNA 靶区中的高可信度变体。一些基因,如 和 ,在多个家庭中被鉴定出来。使用基因本体论过表达分析和蛋白质-蛋白质相互作用网络分析,我们鉴定了与神经发育重要的基因簇和途径。本研究中鉴定的 miRNA 和 miRNA 靶基因可能与神经发育障碍有关,应考虑进一步进行功能研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/77e386dad409/genes-13-01329-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/adcaf3f15056/genes-13-01329-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/70da3a5fedd4/genes-13-01329-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/1a19db2f6999/genes-13-01329-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/83eec0388ab3/genes-13-01329-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/77e386dad409/genes-13-01329-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/adcaf3f15056/genes-13-01329-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/70da3a5fedd4/genes-13-01329-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/1a19db2f6999/genes-13-01329-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/83eec0388ab3/genes-13-01329-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea2/9329941/77e386dad409/genes-13-01329-g005.jpg

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