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The formation of cyclin/CDKs controls the cell-cycle progression via phosphorylation of the target genes, such as tumor suppressor protein retinoblastoma (Rb). The activation of cyclins/CDKs is induced by mitogenic signals and inhibited by the activation of cell-cycle checkpoints in response to DNA damage [8].
Cyclins play the role of activating and chaperoning CDK to specific substrates. They are constantly formed and degraded during the cell cycle. There are different types of cyclins that will chaperone CDK to different, specific substrates depending on what time of the cell cycle the cell is in.
The process consists of four phases: G1 (in which the cell grows and, under appropriate conditions, commits to division), S (in which the DNA is synthesized and chromosomes replicated), G2 (a gap between S and M), and M (in which chromosomes are separated and the cell is divided into two).
In budding yeast, G1 cyclins such as CLN1 and CLN2 are expressed in G1 and S phases, while mitotic cyclins such as CLB1 and CLB2 are expressed in G2 and M phases. We find that the CLBs play a central role in the transition from CLNs to CLBs: the CLBs stimulate their own expression while repressing that of CLNs.
Final answer: Experimental results show the effect of cyclins on the cell cycle by demonstrating the correlation between cyclin levels and cell cycle checkpoints. Cyclins regulate cell transitions and promote progression.

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The cell cycle is tightly regulated by checkpoints between the G1 and S phase, and between the G2 and mitosis. Key proteins, cyclin-dependent kinases and cyclins, control this process. Cyclins are produced at specific times, activating the kinases and allowing progression through the cell cycle.
Cell cycle progression is regulated in part by the sequential activity of various cyclins. The cyclins are regulatory subunits that bind, activate and provide substrate specificity for their catalytic partner serine-threonine kinases, collectively called cyclin-dependent kinases (Cdks) (reviewed in refs. 8 and 9).
Cyclins regulate the activity of their Cdk partners and also modulate their substrate specificity. More than 20 Cdk-related proteins and more than 11 cyclins have been identified in more complex eukaryotes, which has led to the concept that different cell cycle events are regulated by distinct cyclin-Cdk complexes.

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