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The Schizosaccharomyces pombe MBF complex requires heterodimerization for entry into S phase
1Division of Neoplastic Disease Mechanisms, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Abstract:
In Schizosaccharomyces pombe, MBF is a DNA-binding complex suspected to activate the transcription of genes necessary for entry into S phase. The MBF complex contains both p85cdc10 and p72res1/sct1. To obtain a better understanding of how the MBF complex regulates gene expression at the G1/S transition, we have performed a genetic analysis of p72res1. We determined that p72res1 can bind specifically to the cdc22 promoter, when analyzed by gel mobility shift assay, and that the N-terminal 157 amino acids of p72res1 are sufficient for this specific binding. When overexpressed in vivo, a fragment of p72res1 containing this DNA-binding domain could rescue a strain carrying a temperature-sensitive cdc10 allele at the restrictive temperature as well as a strain with a cdc10 null allele. We also determined that the C-terminal region of p72res1 is necessary and sufficient for binding to p85cdc10. Overexpression of the cdc10-binding domain of p72res1 leads to a G1 arrest with a cdc phenotype and a decrease on MBF activity. Overexpression of full-length p72res1 also leads to a growth arrest that can be rescued by overexpression of p85cdc10. These results imply that the MBF activity in vivo is dependent on the interaction of p85cdc10 with p72res1.
Insights
The MBF complex regulates gene expression for cell cycle progression. Its activity depends on the interaction between p85cdc10 and p72res1, crucial for the G1/S transition in Schizosaccharomyces pombe.
Area of Science:
- Molecular Biology
- Cell Cycle Regulation
- Yeast Genetics
Background:
- The MBF complex in Schizosaccharomyces pombe is implicated in activating genes for S phase entry.
- MBF comprises p85cdc10 and p72res1/sct1 subunits.
Purpose of the Study:
- To elucidate the regulatory role of p72res1 in MBF complex function.
- To understand how MBF controls gene expression during the G1/S transition.
Main Methods:
- Genetic analysis of p72res1.
- Gel mobility shift assays to assess DNA binding.
- In vivo overexpression studies of p72res1 fragments.
Main Results:
- p72res1 specifically binds the cdc22 promoter via its N-terminal 157 amino acids.
- Overexpression of the p72res1 DNA-binding domain rescues cdc10 mutants.
- The C-terminal region of p72res1 mediates p85cdc10 interaction, and its overexpression causes G1 arrest.
Conclusions:
- MBF activity is contingent upon the p85cdc10-p72res1 interaction.
- p72res1's DNA-binding and p85cdc10-binding domains have distinct roles in regulating MBF function and cell cycle progression.