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

Thomas Derrien(Universitat Pompeu Fabra), Rory Johnson(Universitat Pompeu Fabra), Giovanni Bussotti(Universitat Pompeu Fabra), Andrea Tanzer(Universitat Pompeu Fabra), Sarah Djebali(Universitat Pompeu Fabra), Hagen Tilgner(Universitat Pompeu Fabra), Grégory Guernec(Institut National de la Recherche Agronomique), David Martı́n(Universitat Pompeu Fabra), Angelika Merkel(Universitat Pompeu Fabra), David G. Knowles(Universitat Pompeu Fabra), Julien Lagarde(Universitat Pompeu Fabra), Lavanya Veeravalli(Agency for Science, Technology and Research), Xiaoan Ruan(Agency for Science, Technology and Research), Yijun Ruan(Agency for Science, Technology and Research), Timo Lassmann(RIKEN Center for Integrative Medical Sciences), Piero Carninci(RIKEN Center for Integrative Medical Sciences), James Brown(University of California, Berkeley), Leonard Lipovich(Wayne State University), José M. González(Wellcome Sanger Institute), Mark Thomas(Wellcome Sanger Institute), Carrie Davis(Cold Spring Harbor Laboratory), Ramin Shiekhattar(The Wistar Institute), T Gingeras(Cold Spring Harbor Laboratory), Tim Hubbard(Wellcome Sanger Institute), Cédric Notredame(Universitat Pompeu Fabra), Jennifer Harrow(Wellcome Sanger Institute), Roderic Guigó(Universitat Pompeu Fabra)
Genome Research
September 1, 2012
Cited by 5,210Open Access
Full Text

Abstract

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.


Related Papers

No related papers found

Powered by citation graph analysis