Cells exit the previous cell cycle and enter a quiescent state.
Cells increase in size and carry out normal metabolic activities.
Cells prepare for DNA replication by synthesizing proteins and organelles.
DNA replication begins at multiple origins of replication along the chromosomes.
DNA polymerase synthesizes new DNA strands in a semiconservative manner.
DNA replication is completed, resulting in the formation of sister chromatids.
Cells continue to grow and synthesize proteins necessary for mitosis.
Checkpoints monitor DNA integrity and ensure proper completion of DNA replication before entering mitosis.
Chromosomes condense, becoming visible under a light microscope.
Centrioles begin to migrate to opposite poles of the cell, forming the spindle apparatus.
Cyclin-CDK complexes phosphorylate target proteins, initiating chromosome condensation and spindle formation.
Checkpoints monitor the integrity of DNA and ensure proper condensation and alignment of chromosomes.
The nuclear envelope ,ER ,Golgi body, breaks down, and the mitotic spindle forms.
Kinetochore proteins assemble on the centromeres of chromosomes, facilitating their attachment to spindle fibers.
Chromosomes align along the metaphase plate, ready for proper segregation during metaphase.
Chromosomes attach to spindle fibers at their kinetochores and begin to move toward the metaphase plate.
Chromosomes align along the metaphase plate, establishing a bipolar spindle.
Sister chromatids separate and move toward opposite poles of the cell due to spindle fiber shortening.
The spindle poles move apart, elongating the cell.
1. Metacentric : inverted V shaped
2. Submetacentric: inverted L shaped
3. Acrocentric:inverted J shaped
4. Telocentric:Inverted I shaped
Chromosomes decondense, and nuclear envelopes form around each set of chromosomes.
The mitotic spindle disassembles, and cytokinesis initiates.
Spindle fibers contract, pulling homologous chromosomes of each bivalent towards opposite poles of the cell. Sister chromatids remain attached at the centromere.
The cytoplasm divides, resulting in two haploid daughter cells, each containing one set of chromosomes.
Actin and myosin filaments assemble at the equatorial plane.
The contractile ring contracts, pinching the cell membrane inward.
The cytoplasm divides, resulting in two daughter cells, each with its nucleus.
Proteins that regulate the progression of the cell cycle by activating cyclin-dependent kinases (CDKs).
Enzymes that regulate the cell cycle by phosphorylating target proteins.
Active complexes formed by the binding of cyclins to CDKs, which phosphorylate target proteins to drive cell cycle progression.
Control mechanisms that monitor the integrity of DNA and other cellular components at key stages of the cell cycle, ensuring proper progression or halting the cycle if abnormalities are detected.
Programmed cell death, which plays a crucial role in removing damaged or unwanted cells from the organism.
Microtubule-organizing centers that play a role in spindle formation during cell division.