An atlas of human long non-coding RNAs with accurate 5' ends.
An atlas of human long non-coding RNAs with accurate 5' ends.
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DOI:
10.1038/nature21374
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发表时间:
2017-03-09
期刊:
影响因子:
64.8
通讯作者:
Forrest AR
中科院分区:
文献类型:
--
作者:
Hon CC;Ramilowski JA;Harshbarger J;Bertin N;Rackham OJ;Gough J;Denisenko E;Schmeier S;Poulsen TM;Severin J;Lizio M;Kawaji H;Kasukawa T;Itoh M;Burroughs AM;Noma S;Djebali S;Alam T;Medvedeva YA;Testa AC;Lipovich L;Yip CW;Abugessaisa I;Mendez M;Hasegawa A;Tang D;Lassmann T;Heutink P;Babina M;Wells CA;Kojima S;Nakamura Y;Suzuki H;Daub CO;de Hoon MJ;Arner E;Hayashizaki Y;Carninci P;Forrest AR
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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影响因子:
56.9
作者:
Carninci, P;Kasukawa, T;Hayashizaki, Y
通讯作者:
Hayashizaki, Y
影响因子:
64.8
作者:
通讯作者:
--
影响因子:
7
作者:
Harrow J;Frankish A;Gonzalez JM;Tapanari E;Diekhans M;Kokocinski F;Aken BL;Barrell D;Zadissa A;Searle S;Barnes I;Bignell A;Boychenko V;Hunt T;Kay M;Mukherjee G;Rajan J;Despacio-Reyes G;Saunders G;Steward C;Harte R;Lin M;Howald C;Tanzer A;Derrien T;Chrast J;Walters N;Balasubramanian S;Pei B;Tress M;Rodriguez JM;Ezkurdia I;van Baren J;Brent M;Haussler D;Kellis M;Valencia A;Reymond A;Gerstein M;Guigó R;Hubbard TJ
通讯作者:
Hubbard TJ
影响因子:
4.5
作者:
Kapusta A;Kronenberg Z;Lynch VJ;Zhuo X;Ramsay L;Bourque G;Yandell M;Feschotte C
通讯作者:
Feschotte C
影响因子:
16.6
作者:
Andersson, Robin;Andersen, Peter Refsing;Sandelin, Albin
通讯作者:
Sandelin, Albin