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CK2 phosphorylation of Bdp1 executes cell cycle-specific RNA polymerase III transcription repression.
- Source :
-
Molecular cell [Mol Cell] 2004 Oct 08; Vol. 16 (1), pp. 81-92. - Publication Year :
- 2004
-
Abstract
- RNA polymerase III (pol III) transcription from the human U6 snRNA promoter can be reconstituted with the recombinant factors SNAPc and Brf2-TFIIIB combined with purified pol III. In this system, CK2 treatment of the pol III complex is required for transcription, whereas treatment of Brf2-TFIIIB is inhibitory. Here we show that CK2 inhibits Brf2-TFIIIB by specifically phosphorylating its Bdp1 component. Bdp1 is phosphorylated by CK2 during mitosis, and this is accompanied by Bdp1 dissociation from the U6 promoter and from chromatin in general and by transcription repression. Remarkably, whereas inhibition of CK2 in mitotic extracts restores pol III transcription, inhibition of CK2 in active S phase extracts debilitates transcription. Thus, CK2 is directed to phosphorylate different targets within the basal pol III transcription machinery at different times during the cell cycle, with opposite transcriptional effects.
- Subjects :
- Casein Kinase II
Chromatin physiology
Conserved Sequence
Gene Expression Regulation physiology
Humans
Mitosis physiology
Mutation
Nuclear Proteins genetics
Phosphorylation
Promoter Regions, Genetic
Protein Structure, Tertiary
Transcription Factor TFIIIB
Transcription, Genetic
Cell Cycle physiology
Nuclear Proteins metabolism
Protein Serine-Threonine Kinases metabolism
RNA Polymerase III metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1097-2765
- Volume :
- 16
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 15469824
- Full Text :
- https://doi.org/10.1016/j.molcel.2004.09.008