wave of nascent transcription on activated human genes

Genome-wide studies reveal that transcription by RNA polymerase II (Pol II) is dynamically regulated. To obtain a comprehensive view of a single transcription cycle, we switched on transcription of five long human genes (>100 kbp) with tumor necrosis factor-α (TNFα) and monitored (using microarra...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2009-10, Vol.106 (43), p.18357-18361
Hauptverfasser: Wada, Youichiro, Ohta, Yoshihiro, Xu, Meng, Tsutsumi, Shuichi, Minami, Takashi, Inoue, Kenji, Komura, Daisuke, Kitakami, Jun'ichi, Oshida, Nobuhiko, Papantonis, Argyris, Izumi, Akashi, Kobayashi, Mika, Meguro, Hiroko, Kanki, Yasuharu, Mimura, Imari, Yamamoto, Kazuki, Mataki, Chikage, Hamakubo, Takao, Shirahige, Katsuhiko, Aburatani, Hiroyuki, Kimura, Hiroshi, Kodama, Tatsuhiko, Cook, Peter R, Ihara, Sigeo
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container_issue 43
container_start_page 18357
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 106
creator Wada, Youichiro
Ohta, Yoshihiro
Xu, Meng
Tsutsumi, Shuichi
Minami, Takashi
Inoue, Kenji
Komura, Daisuke
Kitakami, Jun'ichi
Oshida, Nobuhiko
Papantonis, Argyris
Izumi, Akashi
Kobayashi, Mika
Meguro, Hiroko
Kanki, Yasuharu
Mimura, Imari
Yamamoto, Kazuki
Mataki, Chikage
Hamakubo, Takao
Shirahige, Katsuhiko
Aburatani, Hiroyuki
Kimura, Hiroshi
Kodama, Tatsuhiko
Cook, Peter R
Ihara, Sigeo
description Genome-wide studies reveal that transcription by RNA polymerase II (Pol II) is dynamically regulated. To obtain a comprehensive view of a single transcription cycle, we switched on transcription of five long human genes (>100 kbp) with tumor necrosis factor-α (TNFα) and monitored (using microarrays, RNA fluorescence in situ hybridization, and chromatin immunoprecipitation) the appearance of nascent RNA, changes in binding of Pol II and two insulators (the cohesin subunit RAD21 and the CCCTC-binding factor CTCF), and modifications of histone H3. Activation triggers a wave of transcription that sweeps along the genes at ≈3.1 kbp/min; splicing occurs cotranscriptionally, a major checkpoint acts several kilobases downstream of the transcription start site to regulate polymerase transit, and Pol II tends to stall at cohesin/CTCF binding sites.
doi_str_mv 10.1073/pnas.0902573106
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subjects Antisense elements
Binding Sites
Biological Sciences
CCCTC-Binding Factor
Cell Cycle Proteins - genetics
Cell Cycle Proteins - metabolism
Cells, Cultured
Chromatin Immunoprecipitation
Chromosomal Proteins, Non-Histone - genetics
Chromosomal Proteins, Non-Histone - metabolism
Cohesins
DNA-Binding Proteins
Fluorescence in situ hybridization
Genes
Genomics
Histones
Humans
In Situ Hybridization
Introns
Nuclear Proteins - genetics
Nuclear Proteins - metabolism
Nucleotides
Oligonucleotide Array Sequence Analysis
Phosphoproteins - genetics
Phosphoproteins - metabolism
Repressor Proteins - genetics
Repressor Proteins - metabolism
RNA
RNA polymerase
RNA Polymerase II - metabolism
RNA probes
RNA Splicing
RNA, Messenger - biosynthesis
Signal detection
Splicing
Tiling
Transcription, Genetic
Transcriptional Activation
Tumor Necrosis Factor-alpha - genetics
title wave of nascent transcription on activated human genes
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