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Regulation of Cell Division. Frequency of cell division Varies with cell type Skin cells Skin cells...
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Transcript of Regulation of Cell Division. Frequency of cell division Varies with cell type Skin cells Skin cells...
![Page 1: Regulation of Cell Division. Frequency of cell division Varies with cell type Skin cells Skin cells Divide frequently throughout lifeDivide frequently.](https://reader030.fdocuments.in/reader030/viewer/2022032709/56649ec55503460f94bcf778/html5/thumbnails/1.jpg)
Regulation of Cell Division
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Frequency of cell division
Varies with cell type Skin cells
• Divide frequently throughout life Liver cells
• Retain ability to divide Mature nerve cells & muscle cells
• Do not divide after maturity
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Cell Cycle control Two irreversible points in cell cycle
Replication of genetic material Separation of sister chromatids
Cell can be put on hold at specific checkpoints
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Checkpoint control system
Cell cycle controlled by STOP and GO chemical signals at critical points
Signals indicate if key cellular processes have been completed correctly
3 major checkpoints
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Checkpoint Control System
G1 Can DNA synthesis
begin? G2
Has DNA synthesis been completed correctly?
Commitment to mitosis
M phases Spindle checkpoint Can sister
chromatids separate correctly?
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G1 Checkpoint G1 checkpoint is most critical
Primary decision point• “restriction point”
If cell receives “go” signal, it divides If cell does not receive
“go” signal, cell exits cycle
& switches to Go phase• Non-dividing state
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G0 Phase Non-dividing, differentiated state Most human cells in Go phase
Liver cells• In G0, but can be “called back” to cell
Nerve & muscle cells• Highly specialized; arrested
in G0 & can never divide
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Control of Cell Cycle
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Activation of Cell Division How do cells know when to divide?
Cell communication = signals• Chemical signals in cytoplasm give cue• Signals usually mean proteins
Activators inhibitors
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“Go-ahead” signals Signals that promote cell growth & division
Proteins Internal signals
• “promoting factors” External signals
• “growth factors”
Primary mechanism
of control Phosphorylation
• Kinase enzymes
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Protein signals – Promoting Factors Cyclins
Regulatory proteins Levels cycle in the cell
Cdks Cyclin-dependent kinases Enzyme activates cellular
proteins MPF
• Maturation (mitosis) promoting factor APC
Anaphase promoting complex
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Cyclins & Cdks (1970s-80s)
Interaction of Cdks & different cyclins triggers the stages of the cell cycle
Sir Paul Nurse: cyclins Tim Hunt: Cdks
Leland H. Hartwell: checkpoints
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Cyclin & cyclin dependent kinases
CDKs & cyclin drive cell from one phase to the next in the cell cycle Genes for these regulatory
proteins have been highly conserved through evolution• Proper regulation of cell cycle
is key to life These genes are basically
the same in yeast, insects, plants, & animals
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External signals Growth factors Protein signals released
by body cells that stimulate other cells to divide• Density-dependent
inhibition Crowded cells stop
dividing Mass of cells use up
growth factors• Not enough left to trigger
cell division
• Anchorage dependence To divide cells must be attached
to a substrate
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Growth Factor Signals
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Example of a Growth Factor: Platelet Derived Growth Factor
Made by platelets Binding of PDGF to cell receptors stimulates
fibroblast
cell division Helps heal
wounds
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Growth Factors and Cancer
Proto-oncogenes Normal genes that become oncogenes (cancer-
causing) when mutated Stimulates cell growth If switched on can cause cancer Ex.: RAS (activates cyclins)
Tumor-suppressor genes Inhibit cell division If switched off can cause cancer Ex.: p53 – The cell cycle enforcer – discovered at
Stony Brook by Dr. Arnold Levine
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Cancer & Cell Growth
Cancer is essentially a failure of
cell division control Unrestrained, uncontrolled cell growth
What control is lost? Checkpoint stops Gene p53 plays a key role in G1 checkpoint
• p53 protein halts cell division if it detects damaged DNA Stimulates repair enzymes to fix DNA Forces cell into G0 resting stage Keeps cell in G1 arrest Causes apoptosis of damaged cell
• All cancers have to shut down p53 activity
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Development of Cancer
Cancer develops only after a cell experiences ~ 6 key mutations (“hits”)
1. Unlimited growth• Turn on growth promoter genes
2. Ignore checkpoints• Turn off tumor suppressor genes
3. Escape apoptosis• Turn off suicide genes
4. Immortality = unlimited divisions• Turn on chromosome maintenance genes
5. Promotes blood vessel growth• Turn on blood vessel growth genes
6. Overcome anchor & density dependence• Turn off censor gene
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“Hits” can be triggered by…
UV radiation Chemical exposure Radiation exposure Heat
Cigarette smoke Pollution Age Genetics
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Tumors – mass of abnormal cells Benign tumor
Abnormal cells remain at original sit as a lump• P53 has halted cell division
Most do not cause serious problems & can be removed by surgery
Malignant tumor Cells leave original site
• Lose attachment to nearby cells• Carried by blood & lymph system to other tissues• Start more tumors = metastasis
Impair functions of organs throughout body
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Traditional treatments for cancer Treatments target rapidly
dividing cells High energy radiation &
chemotherapy with toxic drugs
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New “Miracle Drugs” Drugs targeting proteins
(enzymes) found only in tumor cells
Gleevec• Treatment for adult
leukemia & stomach cancer
• 1st successful targeted drug
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Cancers = cell cycle genes
Cancer results from genetic changes that affect the cell cycle Proto-oncogenes
• Normal cellular genes code for proteins that stimulate normal cell growth & division
Oncogenes• Mutations that alter proto-oncogenes cause them
to become cancer-causing genes
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Proto-oncogenes & oncogenes
Genetic change that can turn proto-oncogenes into oncogenes
Removing repression of genes
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Cancers = failures of regulation Cancer cells have escaped cell cycle
controls Do not respond normally to the body’s
control mechanisms• Divide excessively & invade other tissues• If unchecked, they can kill the organism
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Effects of signal pathways
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Multi-step model for cancer Multiple mutations underlie the development of
cancer Several changes must occur at DNA level for cell to
become fully cancerous• Including at least 1 active oncogene &
mutation or loss of several tumor-suppressor genes
• Telomerase is often activated
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p53 gene “Guardian of the Genome”
The “anti-cancer gene” After DNA damage is detected, p53
initiates:• DNA repair• Growth arrest• apoptosis
Almost all cancers
have mutations in p53
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