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An atlas of human long non-coding RNAs with accurate 5′ ends

An atlas of human long non-coding RNAs with accurate 5′ ends
An atlas of human long non-coding RNAs with accurate 5′ ends
Long non-coding RNAs (lncRNAs) are largely heterogeneous and functionally uncharacterized. Here, using FANTOM5 cap analysis of gene expression (CAGE) data, we integrate multiple transcript collections to generate a comprehensive atlas of 27,919 human lncRNA genes with high-confidence 5′ ends and expression profiles across 1,829 samples from the major human primary cell types and tissues. Genomic and epigenomic classification of these lncRNAs reveals that most intergenic lncRNAs originate from enhancers rather than from promoters. Incorporating genetic and expression data, we show that lncRNAs overlapping trait-associated single nucleotide polymorphisms are specifically expressed in cell types relevant to the traits, implicating these lncRNAs in multiple diseases. We further demonstrate that lncRNAs overlapping expression quantitative trait loci (eQTL)-associated single nucleotide polymorphisms of messenger RNAs are co-expressed with the corresponding messenger RNAs, suggesting their potential roles in transcriptional regulation. Combining these findings with conservation data, we identify 19,175 potentially functional lncRNAs in the human genome.
0028-0836
199-204
Hon, Chung-chau
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Ramilowski, Jordan A.
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Bertin, Nicolas
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Rackham, Owen J. L.
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Gough, Julian
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Denisenko, Elena
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Schmeier, Sebastian
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Kasukawa, Takeya
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Noma, Shohei
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Djebali, Sarah
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Alam, Tanvir
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Medvedeva, Yulia A.
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Testa, Alison C.
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Lipovich, Leonard
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Yip, Chi-wai
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Abugessaisa, Imad
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Mendez, Mickaël
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Hasegawa, Akira
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Lassmann, Timo
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Heutink, Peter
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Babina, Magda
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Wells, Christine A.
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Kojima, Soichi
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Nakamura, Yukio
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Suzuki, Harukazu
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Daub, Carsten O.
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De Hoon, Michiel J. L.
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Arner, Erik
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Hayashizaki, Yoshihide
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Carninci, Piero
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Forrest, Alistair R. R.
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Hon, Chung-chau
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Ramilowski, Jordan A.
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Bertin, Nicolas
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Rackham, Owen J. L.
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Gough, Julian
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Denisenko, Elena
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Schmeier, Sebastian
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Poulsen, Thomas M.
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Kasukawa, Takeya
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Noma, Shohei
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Alam, Tanvir
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Lipovich, Leonard
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Yip, Chi-wai
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Abugessaisa, Imad
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Mendez, Mickaël
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Hasegawa, Akira
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Tang, Dave
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Lassmann, Timo
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Heutink, Peter
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Babina, Magda
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Wells, Christine A.
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Kojima, Soichi
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Nakamura, Yukio
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Suzuki, Harukazu
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Daub, Carsten O.
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De Hoon, Michiel J. L.
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Arner, Erik
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Hayashizaki, Yoshihide
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Carninci, Piero
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Forrest, Alistair R. R.
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Hon, Chung-chau, Ramilowski, Jordan A., Harshbarger, Jayson, Bertin, Nicolas, Rackham, Owen J. L., Gough, Julian, Denisenko, Elena, Schmeier, Sebastian, Poulsen, Thomas M., Severin, Jessica, Lizio, Marina, Kawaji, Hideya, Kasukawa, Takeya, Itoh, Masayoshi, Burroughs, A. Maxwell, Noma, Shohei, Djebali, Sarah, Alam, Tanvir, Medvedeva, Yulia A., Testa, Alison C., Lipovich, Leonard, Yip, Chi-wai, Abugessaisa, Imad, Mendez, Mickaël, Hasegawa, Akira, Tang, Dave, Lassmann, Timo, Heutink, Peter, Babina, Magda, Wells, Christine A., Kojima, Soichi, Nakamura, Yukio, Suzuki, Harukazu, Daub, Carsten O., De Hoon, Michiel J. L., Arner, Erik, Hayashizaki, Yoshihide, Carninci, Piero and Forrest, Alistair R. R. (2017) An atlas of human long non-coding RNAs with accurate 5′ ends. Nature, 543 (7644), 199-204. (doi:10.1038/nature21374).

Record type: Article

Abstract

Long non-coding RNAs (lncRNAs) are largely heterogeneous and functionally uncharacterized. Here, using FANTOM5 cap analysis of gene expression (CAGE) data, we integrate multiple transcript collections to generate a comprehensive atlas of 27,919 human lncRNA genes with high-confidence 5′ ends and expression profiles across 1,829 samples from the major human primary cell types and tissues. Genomic and epigenomic classification of these lncRNAs reveals that most intergenic lncRNAs originate from enhancers rather than from promoters. Incorporating genetic and expression data, we show that lncRNAs overlapping trait-associated single nucleotide polymorphisms are specifically expressed in cell types relevant to the traits, implicating these lncRNAs in multiple diseases. We further demonstrate that lncRNAs overlapping expression quantitative trait loci (eQTL)-associated single nucleotide polymorphisms of messenger RNAs are co-expressed with the corresponding messenger RNAs, suggesting their potential roles in transcriptional regulation. Combining these findings with conservation data, we identify 19,175 potentially functional lncRNAs in the human genome.

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More information

Accepted/In Press date: 8 January 2017
e-pub ahead of print date: 1 March 2017
Published date: 9 March 2017

Identifiers

Local EPrints ID: 444309
URI: http://eprints.soton.ac.uk/id/eprint/444309
ISSN: 0028-0836
PURE UUID: a7f53ed9-9221-4605-9573-139df2521df4
ORCID for Owen J. L. Rackham: ORCID iD orcid.org/0000-0002-4390-0872

Catalogue record

Date deposited: 12 Oct 2020 16:31
Last modified: 17 Mar 2024 04:03

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Contributors

Author: Chung-chau Hon
Author: Jordan A. Ramilowski
Author: Jayson Harshbarger
Author: Nicolas Bertin
Author: Julian Gough
Author: Elena Denisenko
Author: Sebastian Schmeier
Author: Thomas M. Poulsen
Author: Jessica Severin
Author: Marina Lizio
Author: Hideya Kawaji
Author: Takeya Kasukawa
Author: Masayoshi Itoh
Author: A. Maxwell Burroughs
Author: Shohei Noma
Author: Sarah Djebali
Author: Tanvir Alam
Author: Yulia A. Medvedeva
Author: Alison C. Testa
Author: Leonard Lipovich
Author: Chi-wai Yip
Author: Imad Abugessaisa
Author: Mickaël Mendez
Author: Akira Hasegawa
Author: Dave Tang
Author: Timo Lassmann
Author: Peter Heutink
Author: Magda Babina
Author: Christine A. Wells
Author: Soichi Kojima
Author: Yukio Nakamura
Author: Harukazu Suzuki
Author: Carsten O. Daub
Author: Michiel J. L. De Hoon
Author: Erik Arner
Author: Yoshihide Hayashizaki
Author: Piero Carninci
Author: Alistair R. R. Forrest

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