MITOSIS
-Cells undergo cell division- to replace cells that have been lost due to maturation/apoptosis
-cells also divide- inresponse to an increased work load
-seen by light microscope- labelled radioactive DNA precursors such as H3 Thymidine- recorded using autoradiographic methods
G0 phase
-most of the cells in this phase are differentiated- specific function
-to leave this phase requires growth factors
Progression through the cell cycle is dependent by cyclin dependent kinase which phosphorylates other substrates and promote cell divison
G1
-longest and most variable cell cycle phase- determines the length of the whole cycle
-requires continuous signals from growth factors
-large amount of growth- large amounts of RNA and protein synthesis
-restriction point at the end of G1 phase- determines whether cell can enter S phase- cell size, condition of the chromosomes, external environment or enter the G0 phase
-p53 stimulates the G1 phase to progress onto S phase
S
-all replication needed to create two cell occurs- DNA and organelles
-synthesis of DNA, replication of centrosomes
-centrosomes are key for cell division – each consists of two centiroles- barrels of 9 triplet microtubules
G2
-phase of chromosome packaging
-synthesis of proteins required for mitosis
-checkpoint determines if all the DNA has been replicated before mitosis and the environments condition are favourable
-mauration promoting factors stimulate progression
MITOSIS
-PROPHASE
-chromosomes first become visible- light microscopy, shorten and condense
-nuclear envelope and nucleolus disintegrate
-centrosome that has already divided goes to opposite pole of the cell
-METAPHASE
-microtubules radiate out from the centrosome into the nuclear area- nuclear spindle
-during metaphase the nuclear spindle is kept under constant tension, as a result of constant amount of tubulin molecules being lost from the negative end in the centromere, and then added to the positive end – through treadmelling the microtubules maintain a constant length
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