Literature DB >> 11551505

TATA binding protein-associated CK2 transduces DNA damage signals to the RNA polymerase III transcriptional machinery.

A Ghavidel1, M C Schultz.   

Abstract

Here we report that RNA polymerase (pol) III transcription is repressed in response to DNA damage by downregulation of TFIIIB, the core component of the pol III transcriptional machinery. Protein kinase CK2 transduces this stress signal to TFIIIB. CK2 associates with and normally activates the TATA binding protein (TBP) subunit of TFIIIB. The beta regulatory subunit of CK2 binds to TBP and is required for high TBP-associated CK2 activity and pol III transcription in unstressed cells. Transcriptional repression induced by DNA damage requires CK2 and coincides with downregulation of TBP-associated CK2 and dissociation of catalytic subunits from TBP-CK2 complexes. Therefore, CK2 is the terminal effector in a signaling pathway that represses pol III transcription when genome integrity is compromised.

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Year:  2001        PMID: 11551505     DOI: 10.1016/s0092-8674(01)00473-1

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  53 in total

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3.  The RNA polymerase III transcriptome revealed by genome-wide localization and activity-occupancy relationships.

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5.  Replication stress checkpoint signaling controls tRNA gene transcription.

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7.  Regulation of NuA4 histone acetyltransferase activity in transcription and DNA repair by phosphorylation of histone H4.

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8.  Phosphorylation and maximal activity of Saccharomyces cerevisiae meiosis-specific transcription factor Ndt80 is dependent on Ime2.

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Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

9.  Transcription elongation factor Spt4 mediates loss of phosphorylated RNA polymerase II transcription in response to DNA damage.

Authors:  Lars E T Jansen; Ana I Belo; Rinske Hulsker; Jaap Brouwer
Journal:  Nucleic Acids Res       Date:  2002-08-15       Impact factor: 16.971

10.  Ability of CK2beta to selectively regulate cellular protein kinases.

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Journal:  Mol Cell Biochem       Date:  2008-06-17       Impact factor: 3.396

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