cell cycle
TRANSCRIPT
• OVERVIEW OF THE CELL CYCLE
• INTRACELLULAR CONTROL OF THE
CELL CYCLE
• EXTRACELLULAR CONTROL OF
CELL DIVISION AND CELL GROWTH
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FLOW OF DISCUSSION1.Overview of the cell cycle
a. G1phase
b. S phase Interphase
c. G2 phase
d. Mitosis phase
* prophase, metaphase, anaphase, telophase, * cytokinesis
Meiosis
2.Intracellular Control of the Cell Cycle
a. Positive: Cyclin- dependent kinase & Cyclins
b. Negative: Rb & p53
3. Extracellular Control of the Cell Cycle
a. Mitogens
b. Growth factors
c. Survival factors
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OVERVIEW: THE KEY ROLES OF CELL
DIVISION
The ability of organisms to reproduce best distinguishes
living things from non-living matter.
The continuity of life is based upon the reproduction of
cells, or cell division.
Cell division is integral part of cell cycle.
INTERPHASE: G1 PHASE
• Recovery from previous division
• Cell doubles its organelles
• Cell grows in size
• Accumulates raw materials for DNA synthesis (DNA replication)
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INTERPHASE: G2 PHASE
• Between DNA replication and onset of mitosis
• Cell synthesizes proteins necessary for division
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CELL CYCLE: MITOSIS PHASE
Mitosis phase includes:
• Mitosis (karyokinesis)
• Nuclear division
• Daughter chromosomes
distributed to two daughter
nuclei
• Cytokinesis
• Cytoplasm division
• Results in two genetically
identical daughter cells
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SIGNIFICANCE OF MITOSIS
• Permits growth and repair.
• In plants it retains the ability to
divide throughout the life of the
plant
• In mammals, mitosis is necessary:
• Fertilized egg becomes an
embryo
• Embryo becomes a fetus
• Allows a cut to heal or a broken
bone to mend
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MITOSIS PHASE: PROPHASEWhat’s happening?
• Chromatin condenses.
• Centrosomes separate, moving to opposite ends of the nucleus
• The centrosomes start to form a framework used to separate the two sister chromatids called the mitotic spindle, that is made of microtubules
• Nucleolus disappears
• Nuclear envelope disintegrates
What the cell looks like?
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MITOSIS PHASE: PROMETAPHASE
What’s happening?
• Nuclear envelope fragments
• Chromosomes become more condensed
• A kinetochore is formed at the centromere, the point where the sister chromatids are attached
• Microtubules attach at the kinetochores
What the cell looks like?
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MITOSIS PHASE: METAPHASE
What’s happening?
• Chromosomes align on
an axis called the
metaphase plate
• Note: the spindle
consists of
microtubules, one
attached to each
chromosome
What the cell looks like?
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MITOSIS PHASE: ANAPHASE
What’s happening?
• Each centromere splits
making two chromatids
free
• Each chromatid moves
toward a pole
• Cell begins to elongate,
caused by microtubules
not associated with the
kinetochore
What the cell looks like?
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MITOSIS PHASE: TELOPHASEWhat’s happening?
• Formation of nuclear membrane and nucleolus
• Short and thick chromosomes begin to elongate to form long and thin chromatin
• Formation of the cleavagefurrow - a shallow groove in the cell near the old metaphase plate
• Cytokinesis = division of the cytoplasm
What the cell looks like?
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RESULTS OF MITOSIS
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• Two daughter nuclei
• Each with same chromosome number as parent cell ( 2n)
• Genetically identical to each other and the parent cell
MEIOSIS
• Formation of Gametes (Eggs & Sperm)
• Called Reduction- division
• Preceded by interphase which includes
chromosome replication
• Two meiotic divisions
• Meiosis I and Meiosis II
• Original cell is diploid (2n)
• Four daughter cells produced that are
haploid (n)
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SIGNIFICANCE OF MEIOSIS
• Two haploid (1n) gametes are brought together through fertilization to form a diploid (2n) zygote
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SIGNIFICANCE OF MEIOSIS
• Meiosis must reduce the chromosome number by half
• Fertilization then restores the 2n number
from mom from dad child
meiosis reduces
genetic content
Too
much!
The
right
number!fatimaArivera
MEIOSIS I: PROPHASE I
Prophase I is further subdivided into
periods known as
•Leptotena
•Zygotena
•Pachytena
•Diplotena
•Diakinesis
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ANAPHASE I
Homologs separate and
move to opposite poles.
Sister chromatids remain
attached at their centromeres.
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TELOPHASE I
Nuclear envelopes
reassemble.
Spindle disappears.
Cytokinesis divides cell into
two.
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MEIOSIS II: ANAPHASE II
Sister chromatids
separate and move
to opposite poles.
Equator
Pole
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MEIOSIS II: TELOPHASE II
Nuclear envelope
assembles.
Chromosomes
decondense.
Spindle disappears.
Cytokinesis divides cell
into two.fatimaArivera
SUMMARY OF MEIOSIS I
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NucleusSpindle
fibersNuclear
envelope
EARLY
PROPHASE
I
LATE PROPHASE I METAPHASE I ANAPHASE I TELOPHASE I &
CYTOKINESIS
SUMMARY OF MEIOSIS II
Prophase II Metaphase II Anaphase II Telophase II 4 I
Undentical
haploid
cellsfatimaArivera
Mitosis Meiosis
Number of
divisions1 2
Number of
daughter cells2 4
Genetically
identical?Yes No
Chromosome # Same as parent Half of parent
Where Somatic cells Germ cells
When Throughout life At sexual maturity
Role Growth and repair Sexual reproduction
COMPARISON OF DIVISIONS
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FLOW OF DISCUSSION1.Overview of the cell cycle
a. G1phase
b. S phase Interphase
c. G2 phase
d. Mitosis phase
* prophase, metaphase, anaphase, telophase, * cytokinesis
Meiosis
2.Intracellular Control of the Cell Cycle
a. Positive: Cyclin- dependent kinase & Cyclins
b. Negative: Rb & p53
3. Extracellular Control of the Cell Cycle
a. Mitogens
b. Growth factors
c. Survival factors
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Intracellular control of the cell
cycle
The cell cycle is controlled by
regulator molecules that either:
promote the process (positive)
stop it from progressing (negative)
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Positive: Cdks & Cyclins
Cyclins◦ The regulatory subunits of the protein
kinases that control the cell cycle
Cyclin-Dependent Kinases (Cdks)◦ The catalytic subunits of the protein
kinases
◦ Must be associated with a cyclin in order to be activated
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Negative: Rb & p53
Tumor suppressor genes
Tumor suppressor gene codes for a
signaling protein in an inhibitory
pathway. If a tumor suppressor gene
mutates, the end result can be
active cell division.
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Negative: Rb & p53
◦ Retinoblastoma protein(Rb)
◦ prevents cell moving into S phase by
binding to a transcription factor
◦ When Rb is phosphorylated it cannot bind
so cell can move into S phase
◦ p53
◦ prevents damaged from dividing (by
inhibiting Rb pathway)
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Retinoblastoma protein (Rb)
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Rb halts the cell cycle by binding E2F. Rb releases its hold on E2F in
response to cell growth to advance the cell cycle.
• group of tumor-suppressor proteins
p53
p53 protein halts cell division if it detects
damaged DNA
options:
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
Cancer is essentially a failure of cell division
control
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p53 is theCell CycleEnforcer
Major molecule players in the
cell cycle control
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Cyclin-dependent
kinases (Cdks)Cyclins
Cdk-cyclin complexP
regulatory proteinsphosphorylates cellular proteins
triggers passage through different stages of cell cycle
Generic cell cycle checkpoints
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Is environment favorable?
Is environment favorable?
Are all DNA replicated?Are all chromosomes
attached to the spindle?
G1
S
G2M
G1 CheckpointG2 CheckpointM Checkpoint
G1 Cdk
G1 Cyclin
PActive G1 Cdk-Cyclin
• Growth factors• Nutritional state of cell• Size of cell
Degraded G1 Cyclin
Mitotic Cdk
Mitotic Cyclin
PActive Mitotic Cdk-Cyclin(MPF)
• Replication completed• DNA integrity
APC
Chromosomes attached at metaphase plate
Degraded Mitotic Cyclin
Control of the Cell Cycle
FLOW OF DISCUSSION
1.Overview of the cell cycle
a. G1phase
b. S phase Interphase
c. G2 phase
d. Mitosis phase
* prophase, metaphase, anaphase, telophase, * cytokinesis
Meiosis
2.Intracellular Control of the Cell Cycle
a. Positive: Cyclin- dependent kinase & Cyclins
b. Negative: Rb & p53
3. Extracellular Control of the Cell Cycle
a. Mitogens
b. Growth factors
c. Survival factors
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EXTRACELLULAR CONTROL OF THE CELL
DIVISION AND CELL GROWTH
• What regulates cell size and cell
number?
• Regulated by extracellular signals
Mitogens stimulate cell division (PDGF)
• Growth factors • stimulate cell growth
• Survival Factors • inhibit apoptosis
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GROWTH FACTORS
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• A signal transduction through phosphatidylinositol pathway
• Kinase cascade leads to increased translation
• Some factors stimulate both growth and cell cycle progression
protein signals released by body
cells that stimulate other cells to
divide
density-dependent inhibition
crowded cells stop dividing
each cell binds a bit of growth factor
not enough activator left to trigger
division in any one cell
anchorage dependence
to divide cells must be attached to a
substrate
“touch sensor” receptors
GROWTH FACTORS
SURVIVAL FACTOR: MYOSTATIN• Myostatins are inhibitory factors that inhibit the proliferation of
myoblast that fuse to form skeletal muscle cells.
• Myostatin Mutants decrease apoptosis in muscle tissue