The schematic model illustrates that G1S cell cycle transition depends Biology Diagrams In the commonly accepted paradigm for control of the mammalian cell cycle, sequential cyclin-dependent kinase (CDK) and cyclin activities drive the orderly transition from G1 to S phase. However, recent studies using different technological approaches and examining a broad range of cancer cell types are challenging this established paradigm. An alternative model is evolving in which cell Finally, a full accounting of how growth regulates the G1/S transition will also likely require a more detailed understanding of the mTOR signaling network and its mechanistic links to G1 control (Liu and Sabatini, 2020). We anticipate the nexus of cell size, growth, and the G1/S transition will be a very active area of research in the coming
The accurate transition from G1 phase of the cell cycle to S phase is crucial for the control of eukaryotic cell proliferation, and its misregulation promotes oncogenesis.
G1/S transition Biology Diagrams
The G1/S transition is a stage in the cell cycle at the boundary between the G1 phase, in which the cell grows, and the S phase, during which DNA is replicated. [1] The cell cycle control system is biochemically based so that the proteins of the mitosis promoting factor The accurate transition from G1 phase of the cell cycle to S phase is crucial for the control of eukaryotic cell proliferation, and its misregulation promotes oncogenesis. During G1 phase, growth-dependent cyclin-dependent kinase (CDK) activity promotes DNA replication and initiates G1-to-S phase transition.
Cyclins regulate cell cycle timing by activating CDKs. Their levels fluctuate throughout the cycle, rising and falling in a phase-specific manner. Different cyclins are associated with distinct stages: cyclin D in G1, cyclin E at the G1/S transition, cyclin A in S and G2, and cyclin B in mitosis. Notably, although the role of endogenous replication stress during the mother S phase provides well-established control of the daughter G1/S transition (19,22,23,40,45), a parallel contribution from ROS-mediated DNA damage arising from mother cell respiration has not been studied (to our knowledge), and may be an important avenue for future Strikingly, the cell-cycle phase targeted most frequently in multistep oncogenesis is the control of G1/S transition. This period includes the late-G1 commitment to replicate the genome and complete the cycle (the restriction point control), and the initiation of DNA replication, events regulated by the so-called `RB pathway'.
