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Cold Spring Harbor Laboratory Press, Genes & Development, 7(27), p. 767-777, 2013

DOI: 10.1101/gad.216200.113

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In vivo live imaging of RNA polymerase II transcription factories in primary cells.

Journal article published in 2013 by Alireza Ghamari, Mariëtte P. C. van de Corput, Supat Thongjuea, Wiggert A. van Cappellen ORCID, Wilfred van Ijcken ORCID, Jeffrey van Haren, Eric Soler, Dirk Eick, Boris Lenhard ORCID, Frank G. Grosveld
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Transcription steps are marked by different modifications of the C-terminal domain of RNA polymerase II (RNAPII). Phosphorylation of Ser5 and Ser7 by cyclin-dependent kinase 7 (CDK7) as part of TFIIH marks initiation, whereas phosphorylation of Ser2 by CDK9 marks elongation. These processes are thought to take place in localized transcription foci in the nucleus, known as "transcription factories,'' but it has been argued that the observed clusters/foci are mere fixation or labeling artifacts. We show that transcription factories exist in living cells as distinct foci by live-imaging fluorescently labeled CDK9, a kinase known to associate with active RNAPII. These foci were observed in different cell types derived from CDK9-mCherry knock-in mice. We show that these foci are very stable while highly dynamic in exchanging CDK9. Chromatin immunoprecipitation (ChIP) coupled with deep sequencing (ChIP-seq) data show that the genome-wide binding sites of CDK9 and initiating RNAPII overlap on transcribed genes. Immunostaining shows that CDK9-mCherry foci colocalize with RNAPII-Ser5P, much less with RNAPII-Ser2P, and not with CDK12 (a kinase reported to be involved in the Ser2 phosphorylation) or with splicing factor SC35. In conclusion, transcription factories exist in living cells, and initiation and elongation of transcripts takes place in different nuclear compartments.