Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Genome Biol. 2022 Feb 7;23(1):48. doi: 10.1186/s13059-022-02621-1.
Circular RNAs (circRNAs), a novel class of poorly conserved non-coding RNAs that regulate gene expression, are highly enriched in the human brain. Despite increasing discoveries of circRNA function in human neurons, the circRNA landscape and function in developing human oligodendroglia, the myelinating cells that govern neuronal conductance, remains unexplored. Meanwhile, improved experimental and computational tools for the accurate identification of circRNAs are needed.
We adopt a published experimental approach for circRNA enrichment and develop CARP (CircRNA identification using A-tailing RNase R approach and Pseudo-reference alignment), a comprehensive 21-module computational framework for accurate circRNA identification and quantification. Using CARP, we identify developmentally programmed human oligodendroglia circRNA landscapes in the HOG oligodendroglioma cell line, distinct from neuronal circRNA landscapes. Numerous circRNAs display oligodendroglia-specific regulation upon differentiation, among which a subclass is regulated independently from their parental mRNAs. We find that circRNA flanking introns often contain cis-regulatory elements for RNA editing and are predicted to bind differentiation-regulated splicing factors. In addition, we discover novel oligodendroglia-specific circRNAs that are predicted to sponge microRNAs, which co-operatively promote oligodendroglia development. Furthermore, we identify circRNA clusters derived from differentiation-regulated alternative circularization events within the same gene, each containing a common circular exon, achieving additive sponging effects that promote human oligodendroglia differentiation.
Our results reveal dynamic regulation of human oligodendroglia circRNA landscapes during early differentiation and suggest critical roles of the circRNA-miRNA-mRNA axis in advancing human oligodendroglia development.
环状 RNA(circRNAs)是一类新型的非编码 RNA,其表达受调控,在人类大脑中高度富集。尽管越来越多的circRNA 在人类神经元中的功能被发现,但在发育中的人类少突胶质细胞(调控神经元传导的髓鞘形成细胞)中,circRNA 的图谱和功能仍未被探索。同时,需要改进用于准确鉴定 circRNA 的实验和计算工具。
我们采用了已发表的 circRNA 富集实验方法,并开发了 CARP(环状 RNA 鉴定使用 A 尾 RNA 酶 R 方法和伪参考比对),这是一种全面的 21 个模块的计算框架,用于准确鉴定和定量 circRNA。使用 CARP,我们在 HOG 少突胶质细胞瘤系中鉴定了发育程序化的人类少突胶质细胞 circRNA 图谱,与神经元 circRNA 图谱不同。大量的 circRNA 在分化过程中表现出少突胶质细胞特异性调节,其中一类是独立于其亲本 mRNA 进行调节的。我们发现 circRNA 侧翼内含子通常含有 RNA 编辑的顺式调控元件,并预测与分化调控的剪接因子结合。此外,我们发现了新的少突胶质细胞特异性 circRNA,它们可能与 microRNAs 结合,从而共同促进少突胶质细胞的发育。此外,我们还鉴定了来自同一基因内分化调节的选择性环状化事件的 circRNA 簇,每个簇都含有一个共同的环状外显子,从而实现了促进人类少突胶质细胞分化的累加海绵效应。
我们的研究结果揭示了人类少突胶质细胞 circRNA 图谱在早期分化过程中的动态调节,并表明 circRNA-miRNA-mRNA 轴在促进人类少突胶质细胞发育中起着关键作用。