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TFIIIB is phosphorylated, disrupted and selectively released from tRNA promoters during mitosis in vivo
Author(s) -
Fairley Jennifer A.,
Scott Pamela H.,
White Robert J.
Publication year - 2003
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/cdg544
Subject(s) - biology , mitosis , phosphorylation , transfer rna , microbiology and biotechnology , promoter , in vivo , genetics , rna , gene , gene expression
Mitosis involves a generalized repression of gene expression. In the case of RNA polymerase III transcription, this is due to phosphorylation‐mediated inactivation of TFIIIB, an essential complex comprising the TATA‐binding protein TBP and the TAF subunits Brf1 and Bdp1. In HeLa cells, this repression is mediated by a mitotic kinase other than cdc2–cyclin B and is antagonized by protein phosphatase 2A. Brf1 is hyperphosphorylated in metaphase‐arrested cells, but remains associated with promoters in condensed chromosomes, along with TBP. In contrast, Bdp1 is selectively released. Repression can be reversed by raising the concentration of Brf1 or Bdp1. The data support a model in which hyperphosphorylation disrupts TFIIIB during mitosis, compromising its ability to support transcription.