Author:
Valen Eivind,Pascarella Giovanni,Chalk Alistair,Maeda Norihiro,Kojima Miki,Kawazu Chika,Murata Mitsuyoshi,Nishiyori Hiromi,Lazarevic Dejan,Motti Dario,Marstrand Troels Torben,Tang Man-Hung Eric,Zhao Xiaobei,Krogh Anders,Winther Ole,Arakawa Takahiro,Kawai Jun,Wells Christine,Daub Carsten,Harbers Matthias,Hayashizaki Yoshihide,Gustincich Stefano,Sandelin Albin,Carninci Piero
Abstract
Finding and characterizing mRNAs, their transcription start sites (TSS), and their associated promoters is a major focus in post-genome biology. Mammalian cells have at least 5–10 magnitudes more TSS than previously believed, and deeper sequencing is necessary to detect all active promoters in a given tissue. Here, we present a new method for high-throughput sequencing of 5′ cDNA tags—DeepCAGE: merging the Cap Analysis of Gene Expression method with ultra-high-throughput sequence technology. We apply DeepCAGE to characterize 1.4 million sequenced TSS from mouse hippocampus and reveal a wealth of novel core promoters that are preferentially used in hippocampus: This is the most comprehensive promoter data set for any tissue to date. Using these data, we present evidence indicating a key role for the Arnt2 transcription factor in hippocampus gene regulation. DeepCAGE can also detect promoters used only in a small subset of cells within the complex tissue.
Publisher
Cold Spring Harbor Laboratory
Subject
Genetics(clinical),Genetics
Cited by
126 articles.
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