Bck2 is a phase-independent activator of cell cycle-regulated genes in yeast

Author

Ferrezuelo, Francisco

Aldea, Martí

Futcher, Bruce

Publication date

2017-01-31T11:46:21Z

2025-01-01

2009



Abstract

During the cell division cycle of the yeast Saccharomyces cerevisiae, the G1-to-S transition depends upon the activation of two transcription factors (SBF and MBF), which are responsible for the cell cycle-regulated expression of more than 200 genes. Bck2 becomes essential in the absence of Cln3, the most upstream activator of this transcriptional program. Here we have used a genome-wide approach to elucidate the targets of Bck2. Our data indicate that Bck2 activates a selection of cell cycle-regulated genes from all cell cycle stages. In contrast, Cln3 activates only G1/S phase genes. Furthermore, Bck2 activates many genes independently of Swi6, the common component of SBF and MBF. Comparison of Bck2 targets with those of other transcription factors suggests that, in addition to SBF and MBF, Bck2 may elicit gene expression via Ste12 and Mcm1. We propose that Bck2 activates its targets by a mechanism fundamentally different from that of Cln3, and that it may be a necessary cofactor for the full expression of a subset of cell cycle-regulated genes.


Thanks to Sylvia Gutiérrez Erlandsson for technical assistance with flow cytometry, Herman Wijnen for providing plasmid pML1 (pRS313-MET3pCLN2), Victor Parro and his lab for sharing the GenePix scanner, and people of the CYC group for their helpful discussions. This work was funded by the Ministerio de Ciencia e Innovación of Spain (Consolider-Ingenio 2010), and the European Union (FEDER). F.F. is a researcher of the Ramón y Cajal program.

Document Type

article
publishedVersion

Language

English

Subjects and keywords

Saccharomyces cerevisiae; Microarrays; Cell cycle; Gene expression; START

Publisher

Landes Bioscience

Related items

Reproducció del document publicat a https://doi.org/10.4161/cc.8.2.7543

Cell Cycle, 2009, vol. 8, núm. 2, p. 239-252

Rights

(c) Landes Bioscience, 2009

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