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Control Points In The Cell Cycle

Three Major Checkpoints


G1 checkpoint:
Life Cycle of Organisms Cell Cycle main checkpoint. If DNA is damaged,
apoptosis will occur. Otherwhise, the cell is
commited to divide when growth signals are
present and when nutrients are available.

G2 checkpoint:
Mitosis Checkpoint. Mitosis will occur if DNA has
replicated properly. Apoptosis will occur if the
DNA is damaged and cannot be repaired.
M checkpoint:
Cell Division
-involves the distribution of identical genetic Spindle assembly checkpoint. Mitosis will not
material or DNA to two daughter cells. continue if chromosomes are not properly aligned
-the DNA is passed along, without dilution
or error, from one generation to the next. G1 Checkpoint – THE RESTRICTION POINT
-functions in: -ensures that the cell is:
1. reproduction a. large enough to divide
2. growth, and b. enough nutrients are available to support
3. repair the resulting daughter cells
4. -go-ahead signal – will usually continue with the
Cell Cycle Cell Cycle
-an orderly sequence of stages that take place -No go-ahead signal – will exit the cell cycle and
between the time a new cell has arisen from the switch to:
division of the parent cell to the point when it has G0 – non-dividing state like in most of the
given rise to two daughter cells. human cell (nerve cell, muscle cell)
-consists of:
1. Interphase – the time when the cell Kinase
performs its usual functions. -a protein which activates or deactivates another
2. Mitosis – a period of nuclear division protein by phosphorylating them.
3. Cytokinesis – division of the cytoplasm -give the go-ahead signals at the G1 and G2
4. checkpoints.
Cell Cycle Control System -must be activated to drive these checkpoints
-driven by a built-in clock that can be adjusted by Cyclin – activating molecule, a protein which
external stimuli (i.e., chemical messages). derives its name from its cyclically fluctuating
-Checkpoint – a critical control point in the Cell concentration in the cell.
Cycle where 'stop' and 'go-ahead' signals can -Cyclin dependent kinases or CDKs
regulate the cell cycle. -Cyclins accumulate during the G1, S, and G2
-Animal Cells have built-in: phases of the cell cycle.
-stop signals that halt the cell cycles
-checkpoints (until overriden by:)
-go-ahead signals
Positive Regulation of the Cell Cycle -involves DNA synthesis for the DNA replication
a. Active molecules – CDKs and cyclin -Beginning of S phase = each chromosome has one
causes the cycle to progress chromatid consisting of a single DNA double helix
b. Cyclins regulate the cell cycle only when -End of S phase = each chromosomes is composed
they are tightly bound to CDKs of two sister chromatids, each having one double
c. To be fully active, the CDK/Cyclin helix
complex must be phosphorylated in specific -The two chromatids of each chromosome remain
locations. attached at the centromere
d. A specific concentration of fully activated -DNA replication produces the duplicated
CDK/Cyclin complexes will allow the cell cycle chromosomes
through the checkpoints.
Phosphorylation – activates by changing its shape Mitotic Phase (Cell Division)
Negative Regulation of the Cell Cycle -occurs during M phase
a. Negative regulators – halt the progression -encompasses both division of the nucleus and
of the cell cycle until problematic conditions are division of the cytoplasm
resolved.
Rb or pRB – retinoblastoma protein >The Spindle
b. Group of tumor suppressor proteins -a structure of the cytoskeleton
common in many cells -pulls the chromatids apart
p53 and p21 – functional molecular masses of the -has spindle fibers made of microtubules
proteins in kilodaltons that are able to assemble and disassemble
p53 – is a multifunction protein that has a major >Centrosome
impact on the commitment of a cell to division. -the primary microtubule organizing the
-it acts when there is damaged DNA in the cells center of a cell
-halts the cell cycle and recruits enzymes to repair -In an animal cell, each centrosome has:
the DNA a. Centrioles – two barrell-like
-can trigger apoptosis when DNA cannot be structures
repaired b. Aster – array of microtubules
(p21 binds to and inhibits the acitivity of
CDK/Cyclin complexes) Mitotic Phase (PROPHASE)
-chromosomes are condensing and becoming
Rb or pRB – retinoblastoma protein visible.
-monitors cell size -Spindle fibers emerge from the centrosomes
-inhibits the function of E2F -Nuclear Envelope breaks down
-Nucleolus disappears
E2F – transcription factors Mitotic Phase (PROMETAPHASE)
-turns on specific genes, allowing the production of -Chromosomes continue to condense
proteins encoded by that gene -Kinetochores appear at the centrosomes
-Mitotic spindle microtubules attach to the
G2 Checkpoint kinetochores
-ensures that DNA replication in S phase has been -Centrosomes move toward opposite poles
successfully completed Mitotic Phase (METAPHASE)
-Mitotic Spindle is fully developed, centrosomes
Metaphase Checkpoint are at the opposite poles of the cell.
-ensures that all of the chromosomes are attached to-Chromosomes are lined up at the metaphase plate
the mitotic spindle by a kinetochore -Each sister chromatid is attached to a spindle fiber
originating from opposite poles

S phase – Synthesis Mitotic Phase (ANAPHASE)


-Cohesion proteins binding the sister chromatids
together break down
-Sister chromatids, now called chromosomes, are
pulled toward opposite ends
-Non kinetochore spindle fibers lengthen,
elongating the cell
Mitotic Phase (TELOPHASE)
-Chromosomes arrive at opposite poles begin to
decondense
-New nuclear envelopes form around the daughter
chromosomes
-The spindle dissapears
-Division of cytoplasm begins

Cytokinesis
-Physical Separation of the cytoplasmic
components into two daughter cells
-New nuclear envelopes form around the daughter
chromosomes
-The spindle disappears
-Division of the cytoplasm begins
Contractile ring – a band of actin filaments, slowly
forms a circular constriction between the two
daughter cells.
Cleavage Furrow – an indentation of the membrane
between the two daughter nuclei

Cytokinesis in plant cell


Cell plate – formed by the fusion of vesicles
produced by the Golgi Apparatus
-grows from the center toward the cell walls

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