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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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Journal ArticleDOI

Regulation of microRNAs function by circular RNAs in human cancer.

TL;DR: The molecular characteristics and biogenesis of circRNAs are reviewed, with a focus on newly identified circ RNAs that may play an important role in human cancer, through their regulation of miR expression.
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Computational approaches for circular RNA analysis.

TL;DR: An overview on different computational analysis tools and pipelines that became available throughout the last years of circRNAs research is provided and a set of valuable validation strategies, in silico as well as in vitro‐based approaches are provided.
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PlantCircNet: a database for plant circRNA–miRNA–mRNA regulatory networks

TL;DR: The identification of several circRNAs to play potential regulatory roles in flower development and response to environmental stress from regulatory networks related with miR156a and AT5G59720, respectively were identified.
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Long non-coding RNAs in vascular biology and disease.

TL;DR: This review summarizes the current knowledge of lncRNA and circRNA functions in vascular biology and disease and discusses their potential use as biomarkers.
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Circular RNA profiling provides insights into their subcellular distribution and molecular characteristics in HepG2 cells.

TL;DR: This study comprehensively analyzed the subcellular distribution/characteristics and the transport mechanism of circRNA, and found that the exosome could selectively package the circRNAs containing the purine-rich 5ʹ-GMWGVWGRAG-3ʹ motif, with the characteristic of ‘garbage dumping’ and ‘intercellular signaling’ functions.
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.
Journal ArticleDOI

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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