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The GENCODE pseudogene resource

delete2012-09-05
delete300
delete
OA
AI
B
Baikang Pei
C
Cristina Sisu
A
Adam Frankish
C
Cédric Howald
L
Lukas Habegger
X
Xinmeng Jasmine Mu
R
Rachel Harte
S
Suganthi Balasubramanian
A
Andrea Tanzer
M
Mark Diekhans
A
Alexandre Reymond
T
Tim Hubbard
J
Jennifer Harrow
M
Mark Gerstein *
DOI:10.1186/gb-2012-13-9-r51delete
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Abstract

Abstract

En 中文
Background: Pseudogenes have long been considered as nonfunctional genomic sequences. However, recent evidence suggests that many of them might have some form of biological activity, and the possibility of functionality has increased interest in their accurate annotation and integration with functional genomics data. Results: As part of the GENCODE annotation of the human genome, we present the first genome-wide pseudogene assignment for protein-coding genes, based on both large-scale manual annotation and in silico pipelines. A key aspect of this coupled approach is that it allows us to identify pseudogenes in an unbiased fashion as well as untangle complex events through manual evaluation. We integrate the pseudogene annotations with the extensive ENCODE functional genomics information. In particular, we determine the expression level, transcription-factor and RNA polymerase II binding, and chromatin marks associated with each pseudogene. Based on their distribution, we develop simple statistical models for each type of activity, which we validate with large-scale RT-PCR-Seq experiments. Finally, we compare our pseudogenes with conservation and variation data from primate alignments and the 1000 Genomes project, producing lists of pseudogenes potentially under selection. Conclusions: At one extreme, some pseudogenes possess conventional characteristics of functionality; these may represent genes that have recently died. On the other hand, we find interesting patterns of partial activity, which may suggest that dead genes are being resurrected as functioning non-coding RNAs. The activity data of each pseudogene are stored in an associated resource, psiDR, which will be useful for the initial identification of potentially functional pseudogenes.
Keywords:
RIBOSOMAL-PROTEIN PSEUDOGENES
GENOME-WIDE SURVEY
PROCESSED PSEUDOGENES
COMPREHENSIVE ANALYSIS
MAMMALIAN GENOMES
ENCODE REGIONS
MOUSE OOCYTES
GENE
ANNOTATION
IDENTIFICATION

Journal

G
Genome Biology
IF:
9.4
Papers:
6.4K
Citations:
7.3W

Organization

University of California System cover
University of California System
Scholars:
37.7W
Papers: 33.8W
Citations: 6.6K
U
University of California Santa Cruz
Scholars:
95
Papers: 39
Citations: 0
Y
Yale University
Scholars:
1.0K
Papers: 411
Citations: 0
W
Wellcome Trust Sanger Institute
Scholars:
19
Papers: 10
Citations: 0
U
university oflausanne
Scholars:
8
Papers: 3
Citations: 0
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