The Cell Cycle - AP Biology · The cell cycle is driven by specific signaling molecules present in...
Transcript of The Cell Cycle - AP Biology · The cell cycle is driven by specific signaling molecules present in...
CAMPBELL BIOLOGY IN FOCUS
© 2014 Pearson Education, Inc.
Urry • Cain • Wasserman • Minorsky • Jackson • Reece
Lecture Presentations by
Kathleen Fitzpatrick and Nicole Tunbridge
9The Cell Cycle
Overview: The Key Roles of Cell Division
The ability of organisms to produce more of their
own kind best distinguishes living things from
nonliving matter
The continuity of life is based on the reproduction
of cells, or cell division
© 2014 Pearson Education, Inc.
Reproduction
In unicellular organisms, division of one cell
reproduces the entire organism
Development and Maintenance
Cell division enables multicellular eukaryotes to
develop from a single cell and, once fully grown, to
renew, repair, or replace cells as needed
Cell division is an integral part of the cell cycle, the
life of a cell from formation to its own division
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.2
(a) Reproduction
100 m
(c) Tissue renewal
(b) Growth anddevelopment
200 m
20 m
Concept 9.1: Most cell division results in genetically identical daughter cells
Most cell division results in the distribution of
identical genetic material—DNA—to two daughter
cells
Mitosis – identical daughter cells
Meiosis – slightly different daughter cells
© 2014 Pearson Education, Inc.
Cellular Organization of the Genetic Material
There are many terms for genetic material
All the DNA in a cell constitutes the cell’s genome
A genome can consist of a single DNA molecule
(common in prokaryotic cells) or a number of DNA
molecules (common in eukaryotic cells)
DNA molecules in a cell can
condense into chromosomes
© 2014 Pearson Education, Inc.
Eukaryotic chromosomes
MORE Terms and Concepts Related to Genetic Material
Eukaryotic chromosomes consist of chromatin, a
complex of DNA and protein
Every eukaryotic species has a characteristic
number of chromosomes in each cell nucleus
Somatic cells (nonreproductive cells) have two sets
of chromosomes
Gametes (reproductive cells: sperm and eggs) have
one set of chromosomes
© 2014 Pearson Education, Inc.
Distribution of Chromosomes During Eukaryotic Cell Division
To prepare for cell division, DNA is replicated, then
chromosomes condense
Each duplicated chromosome has two sister
chromatids (chromatids are identical).
The centromere is where the two chromatids are
most closely attached
© 2014 Pearson Education, Inc.
Centromere 0.5 m
Sisterchromatids
During cell division,
the two sister
chromatids of each
duplicated
chromosome
separate and move
into two nuclei
Once separate, the
chromatids are
called
chromosomes
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.5-1
Centromere
ChromosomalDNA moleculesChromosomes
Chromosome
arm
1
© 2014 Pearson Education, Inc.
Figure 9.5-2
Centromere
Sisterchromatids
ChromosomalDNA moleculesChromosomes
Chromosome
arm
Chromosome duplication
1
2
© 2014 Pearson Education, Inc.
Figure 9.5-3
Centromere
Sisterchromatids
Separation of sisterchromatids
ChromosomalDNA moleculesChromosomes
Chromosome
arm
Chromosome duplication
1
3
2
Eukaryotic cell division consists of
Mitosis, the division of the genetic material in the
nucleus
Cytokinesis, the division of the cytoplasm
© 2014 Pearson Education, Inc.
Meiosis Prepares for Sexual Reproduction
Gametes are produced by a variation of cell division
called meiosis
Meiosis yields nonidentical daughter cells that have
only one set of chromosomes, half as many as the
parent cell
Concept 9.2: The mitotic phase alternates with interphase in the cell cycle
In 1882, the German anatomist Walther Flemming
developed dyes to observe chromosomes during
mitosis and cytokinesis
© 2014 Pearson Education, Inc.
Phases of the Cell Cycle
The cell cycle consists
of
Mitotic (M) phase,
including mitosis and
cytokinesis
Interphase, including
cell growth and
copying of
chromosomes in
preparation for cell
division
© 2014 Pearson Education, Inc.
S(DNA synthesis)
G1
G2
Interphase (about 90% of
the cell cycle) can be
divided into subphases
G1 phase (“first gap”)
S phase (“synthesis”)
G2 phase (“second gap”)
The cell grows during all
three phases, but
chromosomes are
duplicated only during the
S phase © 2014 Pearson Education, Inc.
S(DNA synthesis)
G1
G2
Mitosis is conventionally divided into five phases
Prophase
Prometaphase
Metaphase
Anaphase
Telophase
Cytokinesis overlaps the latter stages of mitosis
© 2014 Pearson Education, Inc.
Video: Animal Mitosis
Video: Microtubules Mitosis
VIDEO: Mitosis
Video: Microtubules Anaphase
Video: Nuclear Envelope
© 2014 Pearson Education, Inc.
Figure 9.7a
Centrosomes(with centriolepairs)
G2 of Interphase Prophase Prometaphase
Chromosomes(duplicated,uncondensed)
Early mitoticspindle
Centromere
Aster
Fragmentsof nuclearenvelope
Nonkinetochoremicrotubules
Kinetochoremicrotubule
KinetochoreNucleolusPlasmamembrane Two sister chromatids of
one chromosome
Nuclearenvelope
10
m
© 2014 Pearson Education, Inc.
Figure 9.7b
Metaphase Anaphase Telophase and
Cytokinesis
Cleavagefurrow
Nucleolusforming
Nuclearenvelopeforming
Spindle Centrosome atone spindle pole
Daughterchromosomes
10
m
Metaphaseplate
© 2014 Pearson Education, Inc.
Figure 9.7c
Centrosomes(with centriolepairs)
G2 of Interphase Prophase
Chromosomes(duplicated,uncondensed)
Early mitoticspindle
Centromere
Aster
NucleolusPlasmamembrane Two sister chromatids of
one chromosome
Nuclearenvelope
© 2014 Pearson Education, Inc.
Figure 9.7d
Prometaphase
Fragmentsof nuclearenvelope
Nonkinetochoremicrotubules
Kinetochoremicrotubule
Kinetochore Spindle Centrosome atone spindle pole
Metaphaseplate
Metaphase
© 2014 Pearson Education, Inc.
Figure 9.7e
Anaphase Telophase and Cytokinesis
Cleavagefurrow
Nucleolusforming
Nuclearenvelopeforming
Daughterchromosomes
© 2014 Pearson Education, Inc.
Figure 9.7f
G2 of Interphase
10
m
© 2014 Pearson Education, Inc.
Figure 9.7g
Prophase
10
m
© 2014 Pearson Education, Inc.
Figure 9.7h
Prometaphase
10
m
© 2014 Pearson Education, Inc.
Figure 9.7i
10
m
Metaphase
© 2014 Pearson Education, Inc.
Figure 9.7j
Anaphase
10
m
© 2014 Pearson Education, Inc.
Figure 9.7k
Telophase and Cytokinesis
10
m
The Mitotic Spindle: A Closer Look
The mitotic spindle is a structure made of
microtubules and associated proteins
It controls chromosome movement during mitosis
In animal cells, assembly of spindle microtubules
begins in the centrosome, the microtubule
organizing center
© 2014 Pearson Education, Inc.
Cytoskeleton Preparations
The centrosome replicates during interphase,
forming two centrosomes that migrate to opposite
ends of the cell during prophase and prometaphase
An aster (radial array of short microtubules) extends
from each centrosome
The spindle includes the centrosomes, the spindle
microtubules, and the asters
© 2014 Pearson Education, Inc.
During prometaphase, some spindle microtubules
attach to the kinetochores of chromosomes and
begin to move the chromosomes
Kinetochores are protein complexes that assemble
on sections of DNA at centromeres
At metaphase, the centromeres of all the
chromosomes are at the metaphase plate, an
imaginary structure at the midway point between
the spindle’s two poles
© 2014 Pearson Education, Inc.
Video: Mitosis Spindle
© 2014 Pearson Education, Inc.
Figure 9.8
Metaphase plate(imaginary)
Chromosomes
Aster
Kinetochoremicrotubules
Kineto-chores
Sisterchromatids
1 m
Centrosome
Overlappingnonkinetochoremicrotubules
Centrosome
Microtubules
0.5 m
© 2014 Pearson Education, Inc.
Figure 9.8a
Chromosomes
1 m
Centrosome
Microtubules
© 2014 Pearson Education, Inc.
Figure 9.8b
Kinetochoremicrotubules
Kinetochores
0.5 m
In anaphase, sister chromatids separate and move
along the kinetochore microtubules toward opposite
ends of the cell
The microtubules shorten by depolymerizing at their
kinetochore ends
Chromosomes are also “reeled in” by motor proteins
at spindle poles, and microtubules depolymerize
after they pass by the motor proteins
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.9
Kinetochore
Experiment
Spindlepole
Results
Kinetochore
Conclusion
Mark
Tubulinsubunits
Chromosome
Motorprotein
Chromosomemovement
Microtubule
© 2014 Pearson Education, Inc.
Figure 9.9a
Kinetochore
Experiment
Spindlepole
Mark
© 2014 Pearson Education, Inc.
Figure 9.9b
Results
Kinetochore
Conclusion
Tubulinsubunits
Chromosome
Motorprotein
Chromosomemovement
Microtubule
Nonkinetochore microtubules from opposite poles
overlap and push against each other, elongating
the cell
At the end of anaphase, duplicate groups of
chromosomes have arrived at opposite ends of the
elongated parent cell
Cytokinesis begins during anaphase or telophase
and the spindle eventually disassembles
© 2014 Pearson Education, Inc.
Cytokinesis: A Closer Look
In animal cells, cytokinesis occurs by a process
known as cleavage, forming a cleavage furrow
In plant cells, a cell plate forms during cytokinesis
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc. Animation: Cytokinesis
© 2014 Pearson Education, Inc. Video: Cytokinesis and Myosin
© 2014 Pearson Education, Inc.
Figure 9.10
(a) Cleavage of an animal cell (SEM)
New cell wall
Contractile ring ofmicrofilaments
Cleavage furrow
Daughter cells
Daughter cells
Cell plate
Wall of parentcell
Vesiclesformingcell plate
100 m
1 m
(b) Cell plate formation in a plant cell (TEM)
© 2014 Pearson Education, Inc.
Figure 9.10a
(a) Cleavage of an animal cell (SEM)
Contractile ring ofmicrofilaments
Cleavage furrow
Daughter cells
100 m
© 2014 Pearson Education, Inc.
Figure 9.10aa
Cleavage furrow 100 m
© 2014 Pearson Education, Inc.
Figure 9.10b
New cell wall
Daughter cells
Cell plate
Wall of parentcell
Vesiclesformingcell plate
1 m
(b) Cell plate formation in a plant cell (TEM)
© 2014 Pearson Education, Inc.
Figure 9.10ba
Wall of parentcell
Vesiclesformingcell plate
1 m
© 2014 Pearson Education, Inc.
Figure 9.11
10 m
Nucleus
Telophase
Nucleolus
Chromosomescondensing Chromosomes
Prometaphase
Cell plate
Prophase
AnaphaseMetaphase
1 2
3 4 5
© 2014 Pearson Education, Inc.
Figure 9.11a
10 m
Nucleus
Nucleolus
Chromosomescondensing
Prophase1
© 2014 Pearson Education, Inc.
Figure 9.11b
10 m2 Prometaphase
Chromosomes
© 2014 Pearson Education, Inc.
Figure 9.11c
10 m3 Metaphase
© 2014 Pearson Education, Inc.
Figure 9.11d
10 m4 Anaphase
© 2014 Pearson Education, Inc.
Figure 9.11e
10 m5 Telophase
Cell plate
Binary Fission in Bacteria
Prokaryotes (bacteria and archaea) reproduce by a
type of cell division called binary fission
In E. coli, the single chromosome replicates,
beginning at the origin of replication
The two daughter chromosomes actively move apart
while the cell elongates
The plasma membrane pinches inward, dividing the
cell into two
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.12-1
1
Origin ofreplication
Two copiesof origin
Bacterialchromosome
Plasmamembrane
Cell wall
E. coli cell
Chromosomereplicationbegins.
© 2014 Pearson Education, Inc.
Figure 9.12-2
1
Origin ofreplication
Two copiesof origin
Bacterialchromosome
Plasmamembrane
Cell wall
E. coli cell
Origin Origin
Chromosomereplicationbegins.
2 One copy of theorigin is now ateach end of thecell.
© 2014 Pearson Education, Inc.
Figure 9.12-3
1
Origin ofreplication
Two copiesof origin
Bacterialchromosome
Plasmamembrane
Cell wall
E. coli cell
Origin Origin
Chromosomereplicationbegins.
2
3
One copy of theorigin is now ateach end of thecell.
Replicationfinishes.
© 2014 Pearson Education, Inc.
Figure 9.12-4
1
Origin ofreplication
Two copiesof origin
Bacterialchromosome
Plasmamembrane
Cell wall
E. coli cell
Origin Origin
Chromosomereplicationbegins.
2
3
4
One copy of theorigin is now ateach end of thecell.
Replicationfinishes.
Two daughtercells result.
The Evolution of Mitosis
Since prokaryotes evolved before eukaryotes,
mitosis probably evolved from binary fission
Certain protists (dinoflagellates, diatoms, and some
yeasts) exhibit types of cell division that seem
intermediate between binary fission and mitosis
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.13Chromosomes
Intact nuclearenvelope
Microtubules
Kinetochoremicrotubule
Intact nuclearenvelope
(a) Dinoflagellates
(b) Diatoms and some yeasts
Concept 9.3: The eukaryotic cell cycle is regulated by a molecular control system
The frequency of cell division varies with the type
of cell
These differences result from regulation at the
molecular level
Cancer cells manage to escape the usual controls
on the cell cycle
© 2014 Pearson Education, Inc.
Evidence for Cytoplasmic Signals
The cell cycle is driven by specific signaling
molecules present in the cytoplasm
Some evidence for this hypothesis comes from
experiments with cultured mammalian cells
Cells at different phases of the cell cycle were fused
to form a single cell with two nuclei at different
stages
Cytoplasmic signals from one of the cells could
cause the nucleus from the second cell to enter the
“wrong” stage of the cell cycle
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.14
G1 nucleusimmediately enteredS phase and DNAwas synthesized.
Experiment
Experiment 1 Experiment 2
Results
S
SS
MG1
MM
G1
G1 nucleus beganmitosis withoutchromosomeduplication.
Conclusion Molecules present in the cytoplasmcontrol the progression to S and M phases.
Checkpoints of the Cell Cycle Control System
The sequential events of the cell cycle are directed
by a distinct cell cycle control system, which is
similar to a timing device of a washing machine
The cell cycle control system is regulated by both
internal and external controls
The clock has specific checkpoints where the cell
cycle stops until a go-ahead signal is received
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.15
M checkpoint
S
M
G1
G2
G1 checkpoint
G2 checkpoint
Controlsystem
For many cells, the G1 checkpoint seems to be the
most important
If a cell receives a go-ahead signal at the G1
checkpoint, it will usually complete the S, G2, and
M phases and divide
If the cell does not receive the go-ahead signal, it
will exit the cycle, switching into a nondividing state
called the G0 phase
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.16
M checkpoint
G1
G1 checkpoint
M
G1
G2
Without go-ahead signal,cell enters G0.
G0
With go-ahead signal,cell continues cell cycle.
(a) G1 checkpoint
Prometaphase
G1
M G2
Without full chromosomeattachment, stop signal isreceived.
(b) M checkpoint
S
G1
M
G1
G2
G2
checkpoint
Metaphase
Anaphase
With full chromosomeattachment, go-ahead signalis received.
© 2014 Pearson Education, Inc.
Figure 9.16a
G1
G1 checkpoint
Without go-ahead signal,cell enters G0.
G0
With go-ahead signal,cell continues cell cycle.
(a) G1 checkpoint
G1
© 2014 Pearson Education, Inc.
Figure 9.16b
M checkpoint
M
G1
G2
Prometaphase
Without full chromosomeattachment, stop signal isreceived.
(b) M checkpoint
M
G1
G2
G2
checkpoint
Metaphase
Anaphase
With full chromosomeattachment, go-ahead signalis received.
The cell cycle is regulated by a set of regulatory
proteins and protein complexes including kinases
and proteins called cyclins
© 2014 Pearson Education, Inc.
An example of an internal signal occurs at the M
phase checkpoint
In this case, anaphase does not begin if any
kinetochores remain unattached to spindle
microtubules
Attachment of all of the kinetochores activates a
regulatory complex, which then activates the enzyme
separase
Separase allows sister chromatids to separate,
triggering the onset of anaphase
© 2014 Pearson Education, Inc.
Some external signals are growth factors, proteins
released by certain cells that stimulate other cells to
divide
For example, platelet-derived growth factor (PDGF)
stimulates the division of human fibroblast cells in
culture
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.17-1
1 A sample ofhuman connectivetissue is cutup into smallpieces.
Petridish
Scalpels
© 2014 Pearson Education, Inc.
Figure 9.17-2
1 A sample ofhuman connectivetissue is cutup into smallpieces.
2 Enzymes digestthe extracellularmatrix, resultingin a suspension offree fibroblasts.
Petridish
Scalpels
© 2014 Pearson Education, Inc.
Figure 9.17-3
1 A sample ofhuman connectivetissue is cutup into smallpieces.
2
3
Enzymes digestthe extracellularmatrix, resultingin a suspension offree fibroblasts.
Cells are transferredto culture vessels.
Petridish
Scalpels
4 PDGF is added tohalf the vessels.
© 2014 Pearson Education, Inc.
Figure 9.17-4
1 A sample ofhuman connectivetissue is cutup into smallpieces.
2
3
4
Enzymes digestthe extracellularmatrix, resultingin a suspension offree fibroblasts.
Cells are transferredto culture vessels. PDGF is added to
half the vessels.
Without PDGF With PDGFCultured fibroblasts(SEM) 10 m
Petridish
Scalpels
© 2014 Pearson Education, Inc.
Figure 9.17a
Cultured fibroblasts(SEM) 10 m
Another example of external signals is density-
dependent inhibition, in which crowded cells stop
dividing
Most animal cells also exhibit anchorage
dependence, in which they must be attached to a
substratum in order to divide
Cancer cells exhibit neither density-dependent
inhibition nor anchorage dependence
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.18
Anchorage dependence: cellsrequire a surface for division
20 m
Density-dependent inhibition:cells divide to fill a gap andthen stop
Density-dependent inhibition:cells form a single layer
20 m
(a) Normal mammalian cells (b) Cancer cells
© 2014 Pearson Education, Inc.
Figure 9.18a
20 m
(a) Normal mammalian cells
© 2014 Pearson Education, Inc.
Figure 9.18b
(b) Cancer cells
20 m
Loss of Cell Cycle Controls in Cancer Cells
Cancer cells do not respond to signals that normally
regulate the cell cycle
Cancer cells may not need growth factors to grow
and divide
They may make their own growth factor
They may convey a growth factor’s signal without the
presence of the growth factor
They may have an abnormal cell cycle control system
© 2014 Pearson Education, Inc.
A normal cell is converted to a cancerous cell by a
process called transformation
Cancer cells that are not eliminated by the immune
system form tumors, masses of abnormal cells within
otherwise normal tissue
If abnormal cells remain only at the original site, the
lump is called a benign tumor
Malignant tumors invade surrounding tissues and
can metastasize, exporting cancer cells to other
parts of the body, where they may form additional
tumors© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.19
1 A tumor growsfrom a singlecancer cell.
Cancer cellsinvadeneighboringtissue.
Cancer cells spreadthrough lymph andblood vessels toother parts of the body.
A small percentageof cancer cells maymetastasize toanother part of the body.
Breast cancer cell(colorized SEM)
Lymphvessel
Bloodvessel
Cancercell
Metastatictumor
Glandulartissue
Tumor
5
m
2 3 4
© 2014 Pearson Education, Inc.
Figure 9.19a
A tumor growsfrom a singlecancer cell.
Cancer cellsinvadeneighboringtissue.
Cancer cells spreadthrough lymph andblood vessels toother parts of the body.
Glandulartissue
Tumor
1 2 3
© 2014 Pearson Education, Inc.
Figure 9.19b
43 Cancer cells spreadthrough lymph andblood vessels toother parts of the body.
A small percentageof cancer cells maymetastasize toanother part of the body.
Lymphvessel
Bloodvessel
Cancercell
Metastatictumor
© 2014 Pearson Education, Inc.
Figure 9.19c
Breast cancer cell(colorized SEM)
5
m
Recent advances in understanding the cell cycle
and cell cycle signaling have led to advances in
cancer treatment
Medical treatments for cancer are becoming more
“personalized” to an individual patient’s tumor
One of the big lessons in cancer research is how
complex cancer is
© 2014 Pearson Education, Inc.
© 2014 Pearson Education, Inc.
Figure 9.UN01
Control Treated
A B CA B C
Amount of fluorescence per cell (fluorescence units)
Nu
mb
er
of
cell
s
200
160
120
80
40
0 200 400 600
0
0 200 400 600
© 2014 Pearson Education, Inc.
Figure 9.UN02
SG1
G2Mitosis
Telophase andCytokinesis
Cytokinesis
MITOTIC (M) PHASE
Anaphase
Metaphase
Prometaphase
Prophase
© 2014 Pearson Education, Inc.
Figure 9.UN03