Related Experiment Video
Updated: May 10, 2026

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
Published on: June 6, 2017
Negative regulation of mitosis by wee1+, a gene encoding a protein kinase homolog
Abstract:
Fission yeast wee1- mutants initiate mitosis at half the cell size of wild type. The wee1+ activity is required to prevent lethal premature mitosis in cells that overproduce the mitotic inducer cdc25+. This lethal phenotype was used to clone wee1+ by complementation. When wee1+ expression is increased, mitosis is delayed until cells grow to a larger size. Thus wee1+ functions as a dose-dependent inhibitor of mitosis, the first such element to be specifically identified and cloned. The carboxy-terminal region of the predicted 112 kd wee1+ protein contains protein kinase consensus sequences, suggesting that negative regulation of mitosis involves protein phosphorylation. Genetic evidence indicates that wee1+ and cdc25+ compete in a control system regulating the cdc2+ protein kinase, which is required for mitotic initiation.
Insights
Fission yeast wee1 mutants initiate mitosis prematurely. Wee1+ protein acts as a dose-dependent inhibitor, delaying mitosis until cells reach a larger size, revealing a key regulator of cell cycle progression.
Area of Science:
- Cell biology
- Molecular genetics
- Biochemistry
Background:
- Fission yeast cell cycle regulation is crucial for proper cell division.
- The protein kinase cdc2+ is essential for initiating mitosis.
- cdc25+ is a known inducer of mitosis.
Purpose of the Study:
- To identify and clone the gene responsible for inhibiting premature mitosis in fission yeast.
- To elucidate the role of the identified gene in cell size control and mitotic entry.
- To understand the regulatory mechanism involving wee1+ and cdc25+ in the cell cycle.
Main Methods:
- Complementation cloning using a lethal premature mitosis phenotype.
- Genetic analysis of gene function and interactions.
- Biochemical analysis of protein domains and kinase activity.
Main Results:
- Fission yeast wee1- mutants initiate mitosis at a significantly smaller cell size.
- Wee1+ activity is essential for preventing lethal premature mitosis induced by cdc25+.
- Increased wee1+ expression delays mitotic entry until cells reach a larger size.
- The wee1+ protein contains kinase consensus sequences, suggesting a role in phosphorylation.
- Wee1+ and cdc25+ compete to regulate the cdc2+ protein kinase.
Conclusions:
- Wee1+ functions as a dose-dependent inhibitor of mitosis, acting as a critical cell size checkpoint.
- The negative regulation of mitosis by wee1+ likely involves protein phosphorylation.
- Wee1+ and cdc25+ form a regulatory system controlling cdc2+ activity and mitotic initiation.
More Related Videos
08:33Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis
Published on: December 5, 2017
12:26Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
Published on: May 3, 2018
Related Concept Videos
Negative Regulator Molecules
Canonical Wnt Signaling Pathway
Inhibition of Cdk Activity
Abnormal Proliferation
The Spindle Assembly Checkpoint
Many proteins function together to control the spindle assembly checkpoint. Mutations affecting these proteins may allow cells to proceed into anaphase prematurely, resulting in the...
Molecular Factors Affecting Cell Division
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...