Intronic RNAs constitute the major fraction of the non-coding RNA in mammalian cells

<p>Abstract</p> <p>Background</p> <p>The function of RNA from the non-coding (the so called “dark matter”) regions of the genome has been a subject of considerable recent debate. Perhaps the most controversy is regarding the function of RNAs found in introns of annotate...

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Main Authors: St Laurent Georges, Shtokalo Dmitry, Tackett Michael R, Yang Zhaoqing, Eremina Tatyana, Wahlestedt Claes, Urcuqui-Inchima Silvio, Seilheimer Bernd, McCaffrey Timothy A, Kapranov Philipp
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/13/504
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author St Laurent Georges
Shtokalo Dmitry
Tackett Michael R
Yang Zhaoqing
Eremina Tatyana
Wahlestedt Claes
Urcuqui-Inchima Silvio
Seilheimer Bernd
McCaffrey Timothy A
Kapranov Philipp
author_facet St Laurent Georges
Shtokalo Dmitry
Tackett Michael R
Yang Zhaoqing
Eremina Tatyana
Wahlestedt Claes
Urcuqui-Inchima Silvio
Seilheimer Bernd
McCaffrey Timothy A
Kapranov Philipp
author_sort St Laurent Georges
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>The function of RNA from the non-coding (the so called “dark matter”) regions of the genome has been a subject of considerable recent debate. Perhaps the most controversy is regarding the function of RNAs found in introns of annotated transcripts, where most of the reads that map outside of exons are usually found. However, it has been reported that the levels of RNA in introns are minor relative to those of the corresponding exons, and that changes in the levels of intronic RNAs correlate tightly with that of adjacent exons. This would suggest that RNAs produced from the vast expanse of intronic space are just pieces of pre-mRNAs or excised introns <it>en route</it> to degradation.</p> <p>Results</p> <p>We present data that challenges the notion that intronic RNAs are mere by-standers in the cell. By performing a highly quantitative RNAseq analysis of transcriptome changes during an inflammation time course, we show that intronic RNAs have a number of features that would be expected from functional, standalone RNA species. We show that there are thousands of introns in the mouse genome that generate RNAs whose overall abundance, which changes throughout the inflammation timecourse, and other properties suggest that they function in yet unknown ways.</p> <p>Conclusions</p> <p>So far, the focus of non-coding RNA discovery has shied away from intronic regions as those were believed to simply encode parts of pre-mRNAs. Results presented here suggest a very different situation – the sequences encoded in the introns appear to harbor a yet unexplored reservoir of novel, functional RNAs. As such, they should not be ignored in surveys of functional transcripts or other genomic studies.</p>
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spelling doaj.art-f162d4cdd90f423bbb0feed1c1516f952022-12-22T01:42:43ZengBMCBMC Genomics1471-21642012-09-0113150410.1186/1471-2164-13-504Intronic RNAs constitute the major fraction of the non-coding RNA in mammalian cellsSt Laurent GeorgesShtokalo DmitryTackett Michael RYang ZhaoqingEremina TatyanaWahlestedt ClaesUrcuqui-Inchima SilvioSeilheimer BerndMcCaffrey Timothy AKapranov Philipp<p>Abstract</p> <p>Background</p> <p>The function of RNA from the non-coding (the so called “dark matter”) regions of the genome has been a subject of considerable recent debate. Perhaps the most controversy is regarding the function of RNAs found in introns of annotated transcripts, where most of the reads that map outside of exons are usually found. However, it has been reported that the levels of RNA in introns are minor relative to those of the corresponding exons, and that changes in the levels of intronic RNAs correlate tightly with that of adjacent exons. This would suggest that RNAs produced from the vast expanse of intronic space are just pieces of pre-mRNAs or excised introns <it>en route</it> to degradation.</p> <p>Results</p> <p>We present data that challenges the notion that intronic RNAs are mere by-standers in the cell. By performing a highly quantitative RNAseq analysis of transcriptome changes during an inflammation time course, we show that intronic RNAs have a number of features that would be expected from functional, standalone RNA species. We show that there are thousands of introns in the mouse genome that generate RNAs whose overall abundance, which changes throughout the inflammation timecourse, and other properties suggest that they function in yet unknown ways.</p> <p>Conclusions</p> <p>So far, the focus of non-coding RNA discovery has shied away from intronic regions as those were believed to simply encode parts of pre-mRNAs. Results presented here suggest a very different situation – the sequences encoded in the introns appear to harbor a yet unexplored reservoir of novel, functional RNAs. As such, they should not be ignored in surveys of functional transcripts or other genomic studies.</p>http://www.biomedcentral.com/1471-2164/13/504
spellingShingle St Laurent Georges
Shtokalo Dmitry
Tackett Michael R
Yang Zhaoqing
Eremina Tatyana
Wahlestedt Claes
Urcuqui-Inchima Silvio
Seilheimer Bernd
McCaffrey Timothy A
Kapranov Philipp
Intronic RNAs constitute the major fraction of the non-coding RNA in mammalian cells
BMC Genomics
title Intronic RNAs constitute the major fraction of the non-coding RNA in mammalian cells
title_full Intronic RNAs constitute the major fraction of the non-coding RNA in mammalian cells
title_fullStr Intronic RNAs constitute the major fraction of the non-coding RNA in mammalian cells
title_full_unstemmed Intronic RNAs constitute the major fraction of the non-coding RNA in mammalian cells
title_short Intronic RNAs constitute the major fraction of the non-coding RNA in mammalian cells
title_sort intronic rnas constitute the major fraction of the non coding rna in mammalian cells
url http://www.biomedcentral.com/1471-2164/13/504
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