A code for transcription initiation in mammalian genomes

被引:189
作者
Frith, Martin C. [1 ,5 ]
Valen, Eivind [2 ,3 ]
Krogh, Anders [2 ,3 ]
Hayashizaki, Yoshihide [4 ,5 ]
Carninci, Piero [4 ,5 ]
Sandelin, Albin [2 ,3 ]
机构
[1] Univ Queensland, Inst Mol Biosci, ARC Ctr Bioinformat, Brisbane, Qld 4072, Australia
[2] Univ Copenhagen, Bioinformat Ctr, Dept Mol Biol & Biotech Res, DK-2200 Kobenhavn N, Denmark
[3] Univ Copenhagen, Innovat Ctr, DK-2200 Copenhagen N, Denmark
[4] RIKEN Wako Inst, Discovery Res Inst, Genome Sci Lab, Wako, Saitama 3510198, Japan
[5] Yokohama Inst Earth Sci, RIKEN, RIKEN Genom Sci Ctr,Tsurumi Ku, Genome Explorat Res Grp,Genome Network Project Co, Kanagawa 2300045, Japan
关键词
D O I
10.1101/gr.6831208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genome-wide detection of transcription start sites (TSSs) has revealed that RNA Polymerase 11 transcription initiates at millions of positions in mammalian genomes. Most core promoters do not have a single TSS, but an array of closely located TSSs with different rates of initiation. As a rule, genes have more than one such core promoter however, defining the boundaries between core promoters is not trivial. These discoveries prompt a re-evaluation of our models for transcription initiation. We describe a new framework for understanding the organization of transcription initiation. We show that initiation events are Clustered oil the chromosomes at Multiple scales-clusters Within clusters-indicating multiple regulatory processes. Within the smallest of such clusters, which can be interpreted as core promoters, the local DNA sequence predicts the relative transcription start usage of each nucleotide with a remarkable 91% accuracy, implying the existence of a DNA code that determines TSS selection. Conversely, the total expression strength of such clusters is only partially determined by the local DNA sequence. Thus, the overall control of transcription call be understood as a combination of large- and small-scale effects; the selection of transcription start sites is largely governed by the local DNA sequence, whereas the transcriptional activity of a locus is regulated at a different level; it is affected by distal features or events Such as enhancers and chromatin remodeling.
引用
收藏
页码:1 / 12
页数:12
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