Differential Expression of Hippocampal Circular RNAs in the BTBR Mouse Model for Autism Spectrum Disorder

被引:0
作者
Silvia Gasparini
Giorgia Del Vecchio
Silvia Gioiosa
Tiziano Flati
Tiziana Castrignano
Ivano Legnini
Valerio Licursi
Laura Ricceri
Maria Luisa Scattoni
Arianna Rinaldi
Carlo Presutti
Cecilia Mannironi
机构
[1] Sapienza University of Rome,Department of Biology and Biotechnology Charles Darwin
[2] CINECA,SCAI
[3] National Research Council,Super Computing Applications and Innovation Department
[4] Sciences University of Tuscia,Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies, IBIOM
[5] National Institute of Health,Department of Ecological and Biological
[6] National Research Council,Institute of Molecular Biology and Pathology
来源
Molecular Neurobiology | 2020年 / 57卷
关键词
Non-coding RNAs; circRNAs; Autism; ASD; RNA-seq; Hippocampus; BTBR;
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学科分类号
摘要
Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental condition with unknown etiology. Recent experimental evidences suggest the contribution of non-coding RNAs (ncRNAs) in the pathophysiology of ASD. In this work, we aimed to investigate the expression profile of the ncRNA class of circular RNAs (circRNAs) in the hippocampus of the BTBR T + tf/J (BTBR) mouse model and age-matched C57BL/6J (B6) mice. Alongside, we analyzed BTBR hippocampal gene expression profile to evaluate possible correlations between the differential abundance of circular and linear gene products. From RNA sequencing data, we identified circRNAs highly modulated in BTBR mice. Thirteen circRNAs and their corresponding linear isoforms were validated by RT-qPCR analysis. The BTBR-regulated circCdh9 was better characterized in terms of molecular structure and expression, highlighting altered levels not only in the hippocampus, but also in the cerebellum, prefrontal cortex, and amygdala. Finally, gene expression analysis of the BTBR hippocampus pinpointed altered biological and molecular pathways relevant for the ASD phenotype. By comparison of circRNA and gene expression profiles, we identified 6 genes significantly regulated at either circRNA or mRNA gene products, suggesting low overall correlation between circRNA and host gene expression. In conclusion, our results indicate a consistent deregulation of circRNA expression in the hippocampus of BTBR mice. ASD-related circRNAs should be considered in functional studies to identify their contribution to the etiology of the disorder. In addition, as abundant and highly stable molecules, circRNAs represent interesting potential biomarkers for autism.
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页码:2301 / 2313
页数:12
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