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Cyclin
Scientists might have asked how cyclin levels are regulated during the cell cycle, what specific role cyclin plays in regulating cell division, and whether abnormalities in cyclin expression or function are associated with diseases like cancer.
The decrease in cyclin levels at a specific point in the cell cycle is typically caused by the cyclin being targeted for degradation by ubiquitin-mediated proteolysis. This process is regulated by the activity of specific enzymes called ubiquitin ligases, which mark the cyclin for destruction by the proteasome. This decrease in cyclin levels is important for progression to the next phase of the cell cycle.
Cyclins are proteins that regulate the cell cycle by binding to cyclin-dependent kinases (CDKs). This binding activates the CDKs, leading to the phosphorylation of target proteins that drive the cell cycle progression.
Cyclin dependent kinases (CDKs) are a family of enzymes that regulate cell cycle progression by phosphorylating target proteins involved in cell division. CDK activity is tightly regulated by the binding of cyclins, which activate their kinase function. CDK-cyclin complexes phosphorylate key proteins to drive cell cycle transitions.
The MPF complex is activated by the phosphorylation of its Cyclin B subunit by Cyclin-dependent kinase (Cdk), causing the complex to become active and initiate mitosis. This phosphorylation is regulated by various factors such as growth factors, DNA damage, and regulatory proteins within the cell cycle.
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Yes, in eukaryotic cells, the timing of the cell cycle is regulated by cyclins. Cyclins are proteins that control the progression of the cell cycle by activating cyclin-dependent kinases (CDKs). The levels of different cyclins fluctuate throughout the cell cycle, signaling the cell to move from one phase to another.
MPF - complex of cyclin and cdk that initiates mitosis by phosphorylating protein and other kinases; highest concentration at metaphase Cdk - levels are constant throughout the cell cycle Cyclin - levels vary because it is broken down by MPF after anaphase
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Electrolyte concentration
MPF promotes the entrance into mitosis from the G2 phase by phosphorylating multiple proteins needed during mitosis. MPF is activated at the end of G2 by a phosphatase, which removes an inhibitory phosphate group added earlier.