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Cell-Type Specific Features of Circular RNA Expression
Thousands of loci in the human and mouse genomes give rise to circular RNA transcripts; at many of these loci, the predominant RNA isoform is a circle. Using an improved computational approach for circular RNA identification, we found widespread circular RNA expression in Drosophila melanogaster and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764148/ https://www.ncbi.nlm.nih.gov/pubmed/24039610 http://dx.doi.org/10.1371/journal.pgen.1003777 |
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author | Salzman, Julia Chen, Raymond E. Olsen, Mari N. Wang, Peter L. Brown, Patrick O. |
author_facet | Salzman, Julia Chen, Raymond E. Olsen, Mari N. Wang, Peter L. Brown, Patrick O. |
author_sort | Salzman, Julia |
collection | PubMed |
description | Thousands of loci in the human and mouse genomes give rise to circular RNA transcripts; at many of these loci, the predominant RNA isoform is a circle. Using an improved computational approach for circular RNA identification, we found widespread circular RNA expression in Drosophila melanogaster and estimate that in humans, circular RNA may account for 1% as many molecules as poly(A) RNA. Analysis of data from the ENCODE consortium revealed that the repertoire of genes expressing circular RNA, the ratio of circular to linear transcripts for each gene, and even the pattern of splice isoforms of circular RNAs from each gene were cell-type specific. These results suggest that biogenesis of circular RNA is an integral, conserved, and regulated feature of the gene expression program. |
format | Online Article Text |
id | pubmed-3764148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37641482013-09-13 Cell-Type Specific Features of Circular RNA Expression Salzman, Julia Chen, Raymond E. Olsen, Mari N. Wang, Peter L. Brown, Patrick O. PLoS Genet Research Article Thousands of loci in the human and mouse genomes give rise to circular RNA transcripts; at many of these loci, the predominant RNA isoform is a circle. Using an improved computational approach for circular RNA identification, we found widespread circular RNA expression in Drosophila melanogaster and estimate that in humans, circular RNA may account for 1% as many molecules as poly(A) RNA. Analysis of data from the ENCODE consortium revealed that the repertoire of genes expressing circular RNA, the ratio of circular to linear transcripts for each gene, and even the pattern of splice isoforms of circular RNAs from each gene were cell-type specific. These results suggest that biogenesis of circular RNA is an integral, conserved, and regulated feature of the gene expression program. Public Library of Science 2013-09-05 /pmc/articles/PMC3764148/ /pubmed/24039610 http://dx.doi.org/10.1371/journal.pgen.1003777 Text en © 2013 Salzman et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Salzman, Julia Chen, Raymond E. Olsen, Mari N. Wang, Peter L. Brown, Patrick O. Cell-Type Specific Features of Circular RNA Expression |
title | Cell-Type Specific Features of Circular RNA Expression |
title_full | Cell-Type Specific Features of Circular RNA Expression |
title_fullStr | Cell-Type Specific Features of Circular RNA Expression |
title_full_unstemmed | Cell-Type Specific Features of Circular RNA Expression |
title_short | Cell-Type Specific Features of Circular RNA Expression |
title_sort | cell-type specific features of circular rna expression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764148/ https://www.ncbi.nlm.nih.gov/pubmed/24039610 http://dx.doi.org/10.1371/journal.pgen.1003777 |
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