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LEQ: Why is the eukaryotic cell cycle regulated?
Key terms: cyclin, growth factor, kinase Reading 5.3 (cancer)
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Activator: Briefly explain why the daughter cells resulting from mitosis are genetically identical to each other and to the original parent cell.
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physical contact with cells Cell signaling: Receptors/enzymes
Cells respond to internal and external signals that regulate cell division. Cell communication: physical contact with cells Cell signaling: Receptors/enzymes soluble chemical signals: Growth factors Survival signals Image: Epidermal Growth Factor (EGF) and Epidermal Growth Factor Receptor (EGFR)
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Internal and external factors: Example
Cell adhesion (stops cycle) Positional information to nucleus integrins
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All cells rely on cell signaling to detect and respond to cues in their environment:
Receptor Tyrosine Kinase (RTKs) activation involves binding to a signal (ligand), the joining together and phosphorylation of proteins. Growth promoting
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Signaling pathways Prevent division or, Promote cell division: Ras pathways promote cell division by turning on genes/proteins associated with the cell cycle
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Cdks coordinate passage through checkpoints:
G1/S Restriction/ enter S G2/M Enter M Spindle/metaphase Exit M
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Cyclins activate Cdks Timing of each phase can be adjusted Failure/DNA damage can result in cell death. apoptosis
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Cell cycles can vary based on stages of development
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Apoptosis is programmed cell death:
Programmed cell death purges damaged cells to prevent disease and shape development Apoptosis is programmed cell death: Initiation of “death” proteins (caspases) self-destructive enzymes Results in progressive cell destruction animation
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Pair Question: Suppose a mutation in a Cdk gene causes the Cdk protein to change shape so it spontaneously activates without the aid of cyclins. Predict what would happen to the cell. Suppose a mutation in a caspase gene causes a Caspase protein to change shape so it spontaneously activates without the aid of a signaling molecule. Predict what would happen to the cell.
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Competition in a tissue for growth factors “sculpts” a tissue
Loss of “tails” Finger webbing webbed fingers
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Leaf senescence (fall) is programmed cell death!
Leaf development is programmed, seasonal cell growth!
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Telomere shortening leads to senescence and programmed cell death
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