The GENCODE v7 catalog of human long noncoding RNAs: Analysis of their gene structure, evolution, and expression

Каталог длинных некодирующих РНК человека GENCODE v7: анализ структуры генов, эволюции и экспрессии
Ramin Shiekhattar, Mark Thomas, Timo Lassmann, T Gingeras, Rory Johnson, Piero Carninci, Jennifer Harrow, José M. González, Andrea Tanzer, Thomas Derrien, Roderic Guigó, Tim Hubbard, Carrie Davis, Sarah Djebali, Julien Lagarde, Giovanni Bussotti, Cédric Notredame, Leonard Lipovich, Hagen Tilgner, Grégory Guernec, David Martı́n, Angelika Merkel, David G. Knowles, Lavanya Veeravalli, Xiaoan Ruan, Yijun Ruan, James Brown
2012-09-01

GENCODE v7gene structure and evolutionlncRNA annotationlong noncoding RNAstissue-specific expression
The human genome contains many thousands of long noncoding RNAs (lncRNAs). While several studies have demonstrated compelling biological and disease roles for individual examples, analytical and experimental approaches to investigate these genes have been hampered by the lack of comprehensive lncRNA annotation. Here, we present and analyze the most complete human lncRNA annotation to date, produced by the GENCODE consortium within the framework of the ENCODE project and comprising 9277 manually annotated genes producing 14,880 transcripts. Our analyses indicate that lncRNAs are generated through pathways similar to that of protein-coding genes, with similar histone-modification profiles, splicing signals, and exon/intron lengths. In contrast to protein-coding genes, however, lncRNAs display a striking bias toward two-exon transcripts, they are predominantly localized in the chromatin and nucleus, and a fraction appear to be preferentially processed into small RNAs. They are under stronger selective pressure than neutrally evolving sequences-particularly in their promoter regions, which display levels of selection comparable to protein-coding genes. Importantly, about one-third seem to have arisen within the primate lineage. Comprehensive analysis of their expression in multiple human organs and brain regions shows that lncRNAs are generally lower expressed than protein-coding genes, and display more tissue-specific expression patterns, with a large fraction of tissue-specific lncRNAs expressed in the brain. Expression correlation analysis indicates that lncRNAs show particularly striking positive correlation with the expression of antisense coding genes. This GENCODE annotation represents a valuable resource for future studies of lncRNAs.
1
Compared with protein-coding genes, lncRNAs show a strong enrichment for two-exon transcripts, predominantly localize to chromatin and the nucleus, and may sometimes produce small RNAs.
2
The GENCODE v7 catalog provides the most complete human lncRNA annotation at the time, covering 9,277 manually annotated genes and 14,880 transcripts.
3
lncRNAs are generated through pathways resembling protein-coding genes, including similar histone-modification profiles, splicing signals, and exon/intron lengths.
4
lncRNAs experience stronger selective pressure than neutrally evolving sequences, especially in promoters, whose conservation is comparable to that of protein-coding genes; approximately one-third originated in primates.
5
lncRNAs generally have lower expression but greater tissue specificity than protein-coding genes, with many tissue-specific lncRNAs expressed in the brain and strong positive correlation with antisense coding genes.

Comprehensive catalog/annotation of human long noncoding RNAs (lncRNAs) produced by GENCODE v7

gene structure, evolutionary conservation and origin, subcellular localization, processing, and expression patterns of human lncRNAs

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2012-09-01
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Authors
Ramin Shiekhattar
Mark Thomas
Timo Lassmann
T Gingeras
Rory Johnson
Piero Carninci
Jennifer Harrow
José M. González
Andrea Tanzer
Thomas Derrien
Roderic Guigó
Tim Hubbard
Carrie Davis
Sarah Djebali
Julien Lagarde
Giovanni Bussotti
Cédric Notredame
Leonard Lipovich
Hagen Tilgner
Grégory Guernec
David Martı́n
Angelika Merkel
David G. Knowles
Lavanya Veeravalli
Xiaoan Ruan
Yijun Ruan
James Brown
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