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
The Bioinformatics Centre, Department of Biology and Biotech Research and Innovation Centre, University of Copenhagen, Ole Maaloes vej 5, DK-2200, Denmark.
Genome Res. 2009 Feb;19(2):255-65. doi: 10.1101/gr.084541.108. Epub 2008 Dec 11.
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.
寻找并鉴定信使核糖核酸(mRNA)、其转录起始位点(TSS)以及相关启动子是后基因组生物学的主要研究重点。哺乳动物细胞的转录起始位点数量比之前认为的至少多5至10个数量级,因此需要更深度的测序才能检测出特定组织中所有活跃的启动子。在此,我们提出了一种用于5' cDNA标签高通量测序的新方法——深度CAGE:将基因表达的帽分析方法与超高通量测序技术相结合。我们应用深度CAGE来鉴定来自小鼠海马体的140万个已测序转录起始位点,并揭示了大量在海马体中优先使用的新型核心启动子:这是迄今为止针对任何组织最全面的启动子数据集。利用这些数据,我们提供了证据表明芳烃受体核转运蛋白2(Arnt2)转录因子在海马体基因调控中起关键作用。深度CAGE还能检测出复杂组织中仅在一小部分细胞中使用的启动子。