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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

An Insulin-Sensitive Circular RNA that Regulates Lifespan in Drosophila.

TL;DR: It is found that accumulation of circRNAs is slowed down in long-lived insulin mutant flies and an important role of circSfl during aging in vivo is revealed and demonstrated.
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Circular RNA circSLC26A4 Accelerates Cervical Cancer Progression via miR-1287-5p/HOXA7 Axis.

TL;DR: It is demonstrated that circSLC26A4 facilitates cervical cancer progression through the QKI/circSLC 26A4/miR-1287-5p/HOXA7 axis, which might bring novel therapeutic strategies for cervical cancer.
Journal ArticleDOI

Closing the circle: current state and perspectives of circular RNA databases.

TL;DR: A comprehensive overview of the current circRNA databases and their content, features, and usability is presented and important suggestions to streamline further research in this growing field are presented.
Journal ArticleDOI

The role of circRNAs in cancers

TL;DR: It is inevitable to further study the interactions between circRNAs and tumors and to develop novelcircRNAs as molecular markers or potential targets, which will provide promising applications in early diagnosis, therapeutic evaluation, prognosis prediction of tumors and even gene therapy for tumors.
Journal ArticleDOI

Circ-ZNF609 regulates G1-S progression in rhabdomyosarcoma.

TL;DR: It is shown that circ-ZNF609 acts by counteracting p-Akt proteasome-dependent degradation, thus working as a new regulator of cell proliferation-related pathways, as opposed to ERMS- derived cells, the circRNA depletion had no cell cycle effects in ARMS-derived cells.
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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