MCB-mediated regulation of cell cycle-specific cdc22+ transcription in fission yeast

• Published in: Molecular genetics and genomics : MGG Vol. 269; no. 6; pp. 765 - 775
• Main Authors: Maqbool, Z, Kersey, P J, Fantes, P A, McInerny, C J
• Format: Journal Article
• Language: English
• Published: Germany Springer Nature B.V 01.09.2003
• Subjects: Base Sequence; Cell Cycle; Cell Cycle Proteins - genetics; Cell Cycle Proteins - metabolism; DNA Footprinting; DNA-Directed RNA Polymerases; G1 Phase; Gene Expression Regulation, Fungal; GTP Phosphohydrolases; Membrane Glycoproteins - genetics; Membrane Proteins; Molecular Sequence Data; Promoter Regions, Genetic - genetics; Ribonucleotide Reductases; RNA polymerase; S Phase; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism; Schizosaccharomyces - genetics; Schizosaccharomyces pombe Proteins; Trans-Activators - genetics; Trans-Activators - metabolism; Transcription Factors; Transcription, Genetic - genetics; Yeast
• ISSN: 1617-4615; 1617-4623
• DOI: 10.1007/s00438-003-0885-4

The cdc22+ gene of the fission yeast, Schizosaccharomyces pombe, encodes the large subunit of ribonucleotide reductase, and is periodically expressed during the mitotic cell cycle, transcript abundance reaching a maximum at the G1-S boundary. This regulation of expression is controlled by a transcription factor complex called DSC1, which binds to MCB motifs (ACGCGT) present in the promoter of cdc22+. cdc22+ has a complex pattern of MCBs, including two clusters of four motifs each, one of which is located within the transcribed region. We show that both clusters of MCBs contribute to the regulation of cdc22+ expression during the cell cycle, each having a different role. The MCB cluster within the transcribed region has the major role in regulating cdc22+, as its removal results in loss of transcription. The upstream cluster, instead, controls cell cycle-specific transcription through a negative function, as its removal results in expression of cdc22+ throughout the cell cycle. Both MCB clusters bind DSC1. We show that the interaction of DSC1 with the MCB cluster within the transcribed region has a high "on-off" rate, suggesting a mechanism by which DSC1 could activate expression, and still allow RNA polymerase to pass during transcription. Finally, we show that both clusters are orientation-dependent in their function. The significance of these results, in the context of MCB-mediated regulation of G1-S expression in fission yeast, is discussed.