Casein kinase 2 inhibits HomolD-directed transcription by Rrn7 in Schizosaccharomyces pombe

Moreira-Ramos, S; Rojas, D.A; Montes M.; Urbina F.; Miralles V.J.; Maldonado E.

Keywords: CK2; HomolD box; Ribosomal protein genes; Rrn7; Transcription

Abstract

In Schizosaccharomyces pombe, ribosomal protein gene (RPG) promoters contain a TATA analogue element called the HomolD box. The HomolDbinding protein Rrn7 forms a complex with the RNA polymerase II machinery. Despite the importance of ribosome biogenesis to cell survival, the mechanisms involved in the regulation of transcription of eukaryotic RPGs are unknown. In this study, we identified Rrn7 as a new substrate of the pleiotropic casein kinase 2 (CK2), which is a regulator of basal transcription. Recombinant Rrn7 from S. pombe, which is often used as a model organism for studying eukaryotic transcription, interacted with CK2 in vitro and in vivo. Furthermore, CK2-mediated phosphorylation of Rrn7 inhibited its HomolD-directed transcriptional activity and ability to bind to an oligonucleotide containing a HomolD box in vitro. Mutation of Rrn7 at Thr67 abolished these effects, indicating that this residue is a critical CK2 phosphorylation site. Finally, Rrn7 interacted with the regulatory subunit of CK2 in vivo, inhibition of CK2 in vivo potentiated ribosomal protein gene transcription, and chromatin immunoprecipitation analyses identified that the catalytic subunit of CK2 was associated with the rpk5 gene promoter in S. pombe. Taken together, these data suggest that CK2 inhibits ribosomal protein gene transcription in S. pombe via phosphorylation of Rrn7 at Thr67.

Más información

Título según WOS: Casein kinase 2 inhibits HomolD-directed transcription by Rrn7 in Schizosaccharomyces pombe
Título según SCOPUS: Casein kinase 2 inhibits HomolD-directed transcription by Rrn7 in Schizosaccharomyces pombe
Título de la Revista: FEBS JOURNAL
Volumen: 282
Número: 3
Editorial: Wiley
Fecha de publicación: 2015
Página de inicio: 491
Página final: 503
Idioma: English
DOI:

10.1111/febs.13157

Notas: ISI, SCOPUS