Genome-wide analysis of mammalian promoter architecture and evolution

Piero Carninci; Albin Sandelin; Boris Lenhard; Shintaro Katayama; Kazuro Shimokawa; Jasmina Ponjavic; Colin A M Semple; Martin S Taylor; Pär G Engström; Martin C Frith; Alistair R R Forrest; Wynand B Alkema; Sin Lam Tan; Charles Plessy; Rimantas Kodzius; Timothy Ravasi; Takeya Kasukawa; Shiro Fukuda; Mutsumi Kanamori-Katayama; Yayoi Kitazume; Hideya Kawaji; Chikatoshi Kai; Mari Nakamura; Hideaki Konno; Kenji Nakano; Salim Mottagui-Tabar; Peter Arner; Alessandra Chesi; Stefano Gustincich; Francesca Persichetti; Harukazu Suzuki; Sean M Grimmond; Christine A Wells; Valerio Orlando; Claes Wahlestedt; Edison T Liu; Matthias Harbers; Jun Kawai; Vladimir B Bajic; David A Hume; Yoshihide Hayashizaki

doi:10.1038/ng1789

Genome-wide analysis of mammalian promoter architecture and evolution

Piero Carninci, Albin Sandelin, Boris Lenhard, Shintaro Katayama, Kazuro Shimokawa, Jasmina Ponjavic, Colin A M Semple, Martin S Taylor, Pär G Engström, Martin C Frith, Alistair R R Forrest, Wynand B Alkema, Sin Lam Tan, Charles Plessy, Rimantas Kodzius, Timothy Ravasi, Takeya Kasukawa, Shiro Fukuda, Mutsumi Kanamori-Katayama, Yayoi KitazumeHideya Kawaji, Chikatoshi Kai, Mari Nakamura, Hideaki Konno, Kenji Nakano, Salim Mottagui-Tabar, Peter Arner, Alessandra Chesi, Stefano Gustincich, Francesca Persichetti, Harukazu Suzuki, Sean M Grimmond, Christine A Wells, Valerio Orlando, Claes Wahlestedt, Edison T Liu, Matthias Harbers, Jun Kawai, Vladimir B Bajic, David A Hume, Yoshihide Hayashizaki

Research output: Contribution to journal › Article › peer-review

Abstract

Mammalian promoters can be separated into two classes, conserved TATA box-enriched promoters, which initiate at a well-defined site, and more plastic, broad and evolvable CpG-rich promoters. We have sequenced tags corresponding to several hundred thousand transcription start sites (TSSs) in the mouse and human genomes, allowing precise analysis of the sequence architecture and evolution of distinct promoter classes. Different tissues and families of genes differentially use distinct types of promoters. Our tagging methods allow quantitative analysis of promoter usage in different tissues and show that differentially regulated alternative TSSs are a common feature in protein-coding genes and commonly generate alternative N termini. Among the TSSs, we identified new start sites associated with the majority of exons and with 3' UTRs. These data permit genome-scale identification of tissue-specific promoters and analysis of the cis-acting elements associated with them.

Original language	English
Pages (from-to)	626-35
Number of pages	10
Journal	Nature Genetics
Volume	38
Issue number	6
DOIs	https://doi.org/10.1038/ng1789
Publication status	Published - 2006

Access to Document

10.1038/ng1789

Cite this

Carninci, P., Sandelin, A., Lenhard, B., Katayama, S., Shimokawa, K., Ponjavic, J., Semple, C. A. M., Taylor, M. S., Engström, P. G., Frith, M. C., Forrest, A. R. R., Alkema, W. B., Tan, S. L., Plessy, C., Kodzius, R., Ravasi, T., Kasukawa, T., Fukuda, S., Kanamori-Katayama, M., ... Hayashizaki, Y. (2006). Genome-wide analysis of mammalian promoter architecture and evolution. Nature Genetics, 38(6), 626-35. https://doi.org/10.1038/ng1789

@article{4bd81d7b48554b1da49bce29ac9ec3da,

title = "Genome-wide analysis of mammalian promoter architecture and evolution",

abstract = "Mammalian promoters can be separated into two classes, conserved TATA box-enriched promoters, which initiate at a well-defined site, and more plastic, broad and evolvable CpG-rich promoters. We have sequenced tags corresponding to several hundred thousand transcription start sites (TSSs) in the mouse and human genomes, allowing precise analysis of the sequence architecture and evolution of distinct promoter classes. Different tissues and families of genes differentially use distinct types of promoters. Our tagging methods allow quantitative analysis of promoter usage in different tissues and show that differentially regulated alternative TSSs are a common feature in protein-coding genes and commonly generate alternative N termini. Among the TSSs, we identified new start sites associated with the majority of exons and with 3' UTRs. These data permit genome-scale identification of tissue-specific promoters and analysis of the cis-acting elements associated with them.",

author = "Piero Carninci and Albin Sandelin and Boris Lenhard and Shintaro Katayama and Kazuro Shimokawa and Jasmina Ponjavic and Semple, {Colin A M} and Taylor, {Martin S} and Engstr{\"o}m, {P{\"a}r G} and Frith, {Martin C} and Forrest, {Alistair R R} and Alkema, {Wynand B} and Tan, {Sin Lam} and Charles Plessy and Rimantas Kodzius and Timothy Ravasi and Takeya Kasukawa and Shiro Fukuda and Mutsumi Kanamori-Katayama and Yayoi Kitazume and Hideya Kawaji and Chikatoshi Kai and Mari Nakamura and Hideaki Konno and Kenji Nakano and Salim Mottagui-Tabar and Peter Arner and Alessandra Chesi and Stefano Gustincich and Francesca Persichetti and Harukazu Suzuki and Grimmond, {Sean M} and Wells, {Christine A} and Valerio Orlando and Claes Wahlestedt and Liu, {Edison T} and Matthias Harbers and Jun Kawai and Bajic, {Vladimir B} and Hume, {David A} and Yoshihide Hayashizaki",

year = "2006",

doi = "10.1038/ng1789",

language = "English",

volume = "38",

pages = "626--35",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Publishing Group",

number = "6",

}

Carninci, P, Sandelin, A, Lenhard, B, Katayama, S, Shimokawa, K, Ponjavic, J, Semple, CAM , Taylor, MS, Engström, PG, Frith, MC, Forrest, ARR, Alkema, WB, Tan, SL, Plessy, C, Kodzius, R, Ravasi, T, Kasukawa, T, Fukuda, S, Kanamori-Katayama, M, Kitazume, Y, Kawaji, H, Kai, C, Nakamura, M, Konno, H, Nakano, K, Mottagui-Tabar, S, Arner, P, Chesi, A, Gustincich, S, Persichetti, F, Suzuki, H, Grimmond, SM, Wells, CA, Orlando, V, Wahlestedt, C, Liu, ET, Harbers, M, Kawai, J, Bajic, VB, Hume, DA & Hayashizaki, Y 2006, 'Genome-wide analysis of mammalian promoter architecture and evolution', Nature Genetics, vol. 38, no. 6, pp. 626-35. https://doi.org/10.1038/ng1789

TY - JOUR

T1 - Genome-wide analysis of mammalian promoter architecture and evolution

AU - Carninci, Piero

AU - Sandelin, Albin

AU - Lenhard, Boris

AU - Katayama, Shintaro

AU - Shimokawa, Kazuro

AU - Ponjavic, Jasmina

AU - Semple, Colin A M

AU - Taylor, Martin S

AU - Engström, Pär G

AU - Frith, Martin C

AU - Forrest, Alistair R R

AU - Alkema, Wynand B

AU - Tan, Sin Lam

AU - Plessy, Charles

AU - Kodzius, Rimantas

AU - Ravasi, Timothy

AU - Kasukawa, Takeya

AU - Fukuda, Shiro

AU - Kanamori-Katayama, Mutsumi

AU - Kitazume, Yayoi

AU - Kawaji, Hideya

AU - Kai, Chikatoshi

AU - Nakamura, Mari

AU - Konno, Hideaki

AU - Nakano, Kenji

AU - Mottagui-Tabar, Salim

AU - Arner, Peter

AU - Chesi, Alessandra

AU - Gustincich, Stefano

AU - Persichetti, Francesca

AU - Suzuki, Harukazu

AU - Grimmond, Sean M

AU - Wells, Christine A

AU - Orlando, Valerio

AU - Wahlestedt, Claes

AU - Liu, Edison T

AU - Harbers, Matthias

AU - Kawai, Jun

AU - Bajic, Vladimir B

AU - Hume, David A

AU - Hayashizaki, Yoshihide

PY - 2006

Y1 - 2006

N2 - Mammalian promoters can be separated into two classes, conserved TATA box-enriched promoters, which initiate at a well-defined site, and more plastic, broad and evolvable CpG-rich promoters. We have sequenced tags corresponding to several hundred thousand transcription start sites (TSSs) in the mouse and human genomes, allowing precise analysis of the sequence architecture and evolution of distinct promoter classes. Different tissues and families of genes differentially use distinct types of promoters. Our tagging methods allow quantitative analysis of promoter usage in different tissues and show that differentially regulated alternative TSSs are a common feature in protein-coding genes and commonly generate alternative N termini. Among the TSSs, we identified new start sites associated with the majority of exons and with 3' UTRs. These data permit genome-scale identification of tissue-specific promoters and analysis of the cis-acting elements associated with them.

AB - Mammalian promoters can be separated into two classes, conserved TATA box-enriched promoters, which initiate at a well-defined site, and more plastic, broad and evolvable CpG-rich promoters. We have sequenced tags corresponding to several hundred thousand transcription start sites (TSSs) in the mouse and human genomes, allowing precise analysis of the sequence architecture and evolution of distinct promoter classes. Different tissues and families of genes differentially use distinct types of promoters. Our tagging methods allow quantitative analysis of promoter usage in different tissues and show that differentially regulated alternative TSSs are a common feature in protein-coding genes and commonly generate alternative N termini. Among the TSSs, we identified new start sites associated with the majority of exons and with 3' UTRs. These data permit genome-scale identification of tissue-specific promoters and analysis of the cis-acting elements associated with them.

U2 - 10.1038/ng1789

DO - 10.1038/ng1789

M3 - Article

C2 - 16645617

VL - 38

SP - 626

EP - 635

JO - Nature Genetics

JF - Nature Genetics

SN - 1061-4036

IS - 6

ER -

Genome-wide analysis of mammalian promoter architecture and evolution

Abstract

Access to Document

Fingerprint

Cite this