Cell division is necessary for the growth of multicellular organisms, the renewal of cells in multicellular organisms, and the production of differentiated cells in multicellular organisms
Prokaryotic cells
Have no nucleus, have a single circular chromosome, divide by binary fission
Eukaryotic cells
Must divide their nucleus as well as the rest of the organelles, genetic material replicates before nucleus divides
Cell division
Can be Mitosis or Meiosis
Mitosis
Results in genetically identical eukaryotic cells (diploid), occurs in somatic cells
Meiosis
Results in genetically different eukaryotic cells with half the genetic material (haploid), occurs in gametes
Haploid cells
Have one complete set of chromosomes
Diploid cells
Have double set of chromosomes
DNA in a cell constitutes the cell's genome, DNA molecules in a eukaryotic cell are packaged into chromosomes
Before cell division
DNA is replicated and the chromosomes condense, each duplicated chromosome has two sister chromatids
Centromere
The narrow "waist" of the duplicated chromosome, where the two chromatids are most closely attached
Cell cycle
Consists of Mitotic (M) phase and Interphase
Interphase
G1 phase, S phase, G2 phase
Mitotic spindle
Structure made of microtubules that controls chromosome movement during mitosis
Centrosome
Microtubule organizing center, contains a pair of centrioles in animal cells
Plant cells do not have centrosomes but they do make perfect mitotic spindles
Metaphase plate
Imaginary structure at the midway point between the spindle's two poles where the chromosomes line up
Kinetochores
Protein complexes associated with centromeres, microtubules attach to kinetochores
Division of cytoplasm, formation of new cell membrane, separation of cells
Cell cycle control system
Directs the sequential events of the cell cycle, has checkpoints where the cell cycle stops until a go-ahead signal is received
G1 checkpoint
Most important checkpoint, if cell receives go-ahead signal it will usually complete the cell cycle, if not it will exit the cycle into G0 phase
Cyclin-dependent protein kinases (Cdks)
Enzymes that catalyze the phosphorylation of various proteins necessary for cell cycle events, their activity is controlled by cyclins
Cyclins
Regulatory proteins essential for the enzymatic activation of Cdks, their concentration fluctuates cyclically throughout the cell cycle
MPF (maturation-promoting factor)
A cyclin-Cdk complex that triggers a cell's passage past the G2 checkpoint into the M phase
Activation of M-Cdk
Requires phosphorylation and dephosphorylation of specific sites, dephosphorylation of inhibitory sites by a phosphatase causes the sudden, explosive increase in M-Cdk activity
Activated M-Cdk
Indirectly activates more M-Cdk, creating a positive feedback loop
Phosphorylated
Having a phosphate group added to a molecule
Removal of inhibitory phosphate groups from a specific protein phosphatase
Activates M-Cdk
Activation of M-Cdk by selective phosphorylation and dephosphorylation
Causes a sudden, explosive increase in M-Cdk activity that rapidly promotes the cell in the M phase
cyclin-Cdk complex
Enzymatically inactive when first formed
Activation of M-Cdk
1. Cdk is phosphorylated at sites necessary for its activation and other sites that inhibit its activity
2. Finally activated by a phosphatase that dephosphorylates the inhibitory phosphate groups
Activated M-Cdk indirectly activates more M-Cdk
Activated M-Cdk
Phosphorylates and activates more molecules of activating phosphatase, which can now activate more M-Cdk complexes
Activation of M-Cdk is explosive
Sudden drop in cyclin concentration during mitosis
1. Due to its rapid degradation by the ubiquitin-dependent proteolytic system
2. Each molecule of M-cyclin covalently binds many ubiquitin molecules and leads it to degradation in the proteasome
3. Ubiquitination of cyclin ultimately causes its destruction
Destruction of cyclin
Inactivates Cdk
Anaphase promoting complex (APC)
Protein complex that adds ubiquitin to cyclin and other proteins involved in mitotic regulation
APC is not active at all stages of the cell cycle
At advanced phases of mitosis, M-Cdk is activated, which leads to APC complex activation, which leads to ubiquitination and degradation of M-cyclin and thus inactivation of M-Cdk