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Open AccessJournal ArticleDOI

Circular RNAs Are the Predominant Transcript Isoform from Hundreds of Human Genes in Diverse Cell Types

TLDR
By deep sequencing of RNA from a variety of normal and malignant human cells, this work suggests that a non-canonical mode of RNA splicing, resulting in a circular RNA isoform, is a general feature of the gene expression program in human cells.
Abstract
Most human pre-mRNAs are spliced into linear molecules that retain the exon order defined by the genomic sequence. By deep sequencing of RNA from a variety of normal and malignant human cells, we found RNA transcripts from many human genes in which the exons were arranged in a non-canonical order. Statistical estimates and biochemical assays provided strong evidence that a substantial fraction of the spliced transcripts from hundreds of genes are circular RNAs. Our results suggest that a non-canonical mode of RNA splicing, resulting in a circular RNA isoform, is a general feature of the gene expression program in human cells.

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Citations
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Circular RNA TTN Acts As a miR-432 Sponge to Facilitate Proliferation and Differentiation of Myoblasts via the IGF2/PI3K/AKT Signaling Pathway.

TL;DR: Results showed that circTTN promoted proliferation and differentiation of bovine primary myoblasts via competitively combining with miR-432 to activate the IGF2/phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway.
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A novel circFMN2 promotes tumor proliferation in CRC by regulating the miR-1182/hTERT signaling pathways

TL;DR: circFMN2 is a central component linking circRNAs to progression of CRC via a miR-1182/hTERT axis and is provided a novel basis for targeted therapy for CRC from the aspect of circRNA-miRNA-mRNA interaction.
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Non-coding RNA: a potential biomarker and therapeutic target for sepsis.

TL;DR: Non-coding RNAs provide a new insight into sepsis and could become the novel therapeutic targets in the future to further understanding of the disease process.
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Lncing Epigenetic Control of Transcription to Cardiovascular Development and Disease

TL;DR: The growing roles of long noncoding RNAs in different aspects of cardiovascular development as well as pathological responses during injury or disease are discussed and the exciting potential of this novel class of transcripts as biomarkers and novel therapeutic targets for cardiovascular diseases is explored.
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The emerging landscape of circular RNA in cardiovascular diseases.

TL;DR: The biogenesis, properties and biological function of circRNAs are reviewed, and their roles in cardiovascular disorders are summarized.
References
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Journal ArticleDOI

A coding-independent function of gene and pseudogene mRNAs regulates tumour biology

TL;DR: It is found that PTENP1 is biologically active as it can regulate cellular levels of PTEN and exert a growth-suppressive role, and this analysis extended to other cancer-related genes that possess pseudogenes, and revealed a non-coding function for mRNAs.
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Circular transcripts of the testis-determining gene Sry in adult mouse testis

TL;DR: It is suggested that the circles arise from normal splicing processes as a consequence of the unusual genomic structure surrounding the Sry locus in the mouse.
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Mis-splicing yields circular RNA molecules.

TL;DR: To the knowledge, this is the first case of circular transcripts being processed from nuclear pre‐mRNA in eukaryotes, and might represent a novel aspect of gene expression and hold some interesting clues about the splicing mechanism.
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miRNA-dependent gene silencing involving Ago2-mediated cleavage of a circular antisense RNA

TL;DR: This study provides the first evidence for non‐coding antisense transcripts as functional miRNA targets, and a novel regulatory mechanism involving a positive correlation between mRNA and antisense circular RNA levels.
Journal ArticleDOI

Expression of Linear and Novel Circular Forms of an INK4/ARF-Associated Non-Coding RNA Correlates with Atherosclerosis Risk

TL;DR: The results identify novel circular RNA products emanating from the ANRIL locus and suggest causal variants at 9p21.3 regulate INK4/ARF expression and ASVD risk by modulating ANRil expression and/or structure.
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