Chapter 12. The Cell Cycle презентация

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Overview: The Key Roles of Cell Division The ability of organisms to reproduce best distinguishes living things from nonliving matter The continuity of life is based on the reproduction of cells,

Слайд 1Chapter 12
The Cell Cycle


Слайд 2Overview: The Key Roles of Cell Division
The ability of organisms to

reproduce best distinguishes living things from nonliving matter
The continuity of life is based on the reproduction of cells, or cell division

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 3Fig. 12-1


Слайд 4In unicellular organisms, division of one cell reproduces the entire organism
Multicellular

organisms depend on cell division for:
Development from a fertilized cell
Growth
Repair
Cell division is an integral part of the cell cycle, the life of a cell from formation to its own division

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 5Fig. 12-2
100 µm
200 µm
20 µm
(a) Reproduction
(b) Growth and
development
(c)

Tissue renewal

Слайд 6Fig. 12-2a
100 µm
(a) Reproduction


Слайд 7Fig. 12-2b
200 µm
(b) Growth and development


Слайд 8Fig. 12-2c
20 µm
(c) Tissue renewal


Слайд 9Concept 12.1: Cell division results in genetically identical daughter cells
Most cell

division results in daughter cells with identical genetic information, DNA
A special type of division produces nonidentical daughter cells (gametes, or sperm and egg cells)

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 10Cellular Organization of the 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 are packaged into chromosomes

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 11Fig. 12-3
20 µm


Слайд 12Every 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 half as many chromosomes as somatic cells
Eukaryotic chromosomes consist of chromatin, a complex of DNA and protein that condenses during cell division

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 13Distribution of Chromosomes During Eukaryotic Cell Division
In preparation for cell division,

DNA is replicated and the chromosomes condense
Each duplicated chromosome has two sister chromatids, which separate during cell division
The centromere is the narrow “waist” of the duplicated chromosome, where the two chromatids are most closely attached

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 14Fig. 12-4
0.5 µm
Chromosomes
Chromosome
duplication
(including DNA
synthesis)
Chromo-
some arm
Centromere
Sister
chromatids
DNA molecules
Separation of
sister chromatids
Centromere
Sister chromatids


Слайд 15Eukaryotic cell division consists of:
Mitosis, the division of the nucleus
Cytokinesis, the

division of the cytoplasm
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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 16Concept 12.2: 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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 17Phases of the Cell Cycle
The cell cycle consists of
Mitotic (M) phase

(mitosis and cytokinesis)
Interphase (cell growth and copying of chromosomes in preparation for cell division)

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 18Interphase (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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 19Fig. 12-5
S
(DNA synthesis)
MITOTIC
(M) PHASE
Mitosis
Cytokinesis
G1
G2
INTERPHASE


Слайд 20Mitosis is conventionally divided into five phases:
Prophase
Prometaphase
Metaphase
Anaphase
Telophase
Cytokinesis is well underway by

late telophase

BioFlix: Mitosis

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 21




Fig. 12-6
G2 of Interphase
Centrosomes
(with centriole
pairs)
Chromatin
(duplicated)
Nucleolus
Nuclear
envelope
Plasma
membrane
Early mitotic
spindle
Aster
Centromere
Chromosome, consisting
of two sister chromatids

Prophase

Prometaphase
Fragments
of

nuclear
envelope

Nonkinetochore
microtubules

Kinetochore

Kinetochore
microtubule

Metaphase

Metaphase
plate

Spindle

Centrosome at
one spindle pole


Anaphase

Daughter
chromosomes

Telophase and Cytokinesis

Cleavage
furrow

Nucleolus
forming

Nuclear
envelope
forming


Слайд 22


Prophase


Fig. 12-6a
Prometaphase
G2 of Interphase


Слайд 23


Fig. 12-6b
Prometaphase
Prophase
G2 of Interphase
Nonkinetochore
microtubules
Fragments
of nuclear
envelope
Aster
Centromere

Early mitotic
spindle
Chromatin
(duplicated)
Centrosomes
(with centriole
pairs)
Nucleolus
Nuclear
envelope
Plasma
membrane
Chromosome, consisting
of two sister chromatids
Kinetochore
Kinetochore
microtubule


Слайд 24


Fig. 12-6c
Metaphase
Anaphase
Telophase and Cytokinesis


Слайд 25


Fig. 12-6d
Metaphase
Anaphase
Telophase and Cytokinesis
Cleavage
furrow
Nucleolus
forming
Metaphase
plate
Centrosome at
one spindle pole
Spindle
Daughter
chromosomes
Nuclear
envelope
forming


Слайд 26The Mitotic Spindle: A Closer Look
The mitotic spindle is an apparatus

of microtubules that controls chromosome movement during mitosis
During prophase, assembly of spindle microtubules begins in the centrosome, the microtubule organizing center
The centrosome replicates, forming two centrosomes that migrate to opposite ends of the cell, as spindle microtubules grow out from them

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 27An aster (a radial array of short microtubules) extends from each

centrosome
The spindle includes the centrosomes, the spindle microtubules, and the asters

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 28During prometaphase, some spindle microtubules attach to the kinetochores of chromosomes

and begin to move the chromosomes
At metaphase, the chromosomes are all lined up at the metaphase plate, the midway point between the spindle’s two poles

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 29Fig. 12-7
Microtubules
Chromosomes
Sister
chromatids
Aster
Metaphase
plate
Centrosome
Kineto-
chores
Kinetochore
microtubules
Overlapping
nonkinetochore
microtubules
Centrosome
1 µm
0.5 µm


Слайд 30In 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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 31


Fig. 12-8
EXPERIMENT
Kinetochore
RESULTS
CONCLUSION
Spindle
pole
Mark
Chromosome
movement
Kinetochore
Microtubule
Motor
protein
Chromosome
Tubulin
subunits


Слайд 32Fig. 12-8a
Kinetochore
Spindle
pole
Mark

EXPERIMENT

RESULTS


Слайд 33Fig. 12-8b
Kinetochore
Microtubule
Tubulin
Subunits
Chromosome
Chromosome
movement
Motor
protein

CONCLUSION


Слайд 34Nonkinetochore microtubules from opposite poles overlap and push against each other,

elongating the cell
In telophase, genetically identical daughter nuclei form at opposite ends of the cell

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 35Cytokinesis: 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

Animation: Cytokinesis

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 36Video: Sea Urchin (Time Lapse)
Video: Animal Mitosis
Copyright © 2008 Pearson Education,

Inc., publishing as Pearson Benjamin Cummings

Слайд 37Fig. 12-9
Cleavage furrow
100 µm
Contractile ring of
microfilaments
Daughter cells
(a) Cleavage of an animal

cell (SEM)

(b) Cell plate formation in a plant cell (TEM)

Vesicles
forming
cell plate

Wall of
parent cell

Cell plate

Daughter cells

New cell wall

1 µm


Слайд 38Cleavage furrow
Fig. 12-9a
100 µm
Daughter cells
(a) Cleavage of an animal cell (SEM)
Contractile

ring of
microfilaments

Слайд 39Fig. 12-9b
Daughter cells
(b) Cell plate formation in a plant cell (TEM)
Vesicles
forming
cell

plate

Wall of
parent cell

New cell wall

Cell plate

1 µm


Слайд 40Fig. 12-10
Chromatin
condensing
Metaphase
Anaphase
Telophase
Prometaphase
Nucleus
Prophase

1

2

3

5

4
Nucleolus
Chromosomes
Cell plate
10 µm


Слайд 41Fig. 12-10a
Nucleus
Prophase

1
Nucleolus
Chromatin
condensing


Слайд 42Fig. 12-10b
Prometaphase

2
Chromosomes


Слайд 43Fig. 12-10c
Metaphase

3


Слайд 44Fig. 12-10d
Anaphase

4


Слайд 45Fig. 12-10e
Telophase

5
Cell plate
10 µm


Слайд 46Binary Fission
Prokaryotes (bacteria and archaea) reproduce by a type of cell

division called binary fission
In binary fission, the chromosome replicates (beginning at the origin of replication), and the two daughter chromosomes actively move apart

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 47Fig. 12-11-1
Origin of
replication
Two copies
of origin
E. coli cell
Bacterial
chromosome
Plasma
membrane
Cell wall


Слайд 48Fig. 12-11-2
Origin of
replication
Two copies
of origin
E. coli cell
Bacterial
chromosome
Plasma
membrane
Cell wall
Origin
Origin


Слайд 49Fig. 12-11-3
Origin of
replication
Two copies
of origin
E. coli cell
Bacterial
chromosome
Plasma
membrane
Cell wall
Origin
Origin


Слайд 50Fig. 12-11-4
Origin of
replication
Two copies
of origin
E. coli cell
Bacterial
chromosome
Plasma
membrane
Cell wall
Origin
Origin


Слайд 51The Evolution of Mitosis
Since prokaryotes evolved before eukaryotes, mitosis probably evolved

from binary fission
Certain protists exhibit types of cell division that seem intermediate between binary fission and mitosis

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 52Fig. 12-12
(a) Bacteria
Bacterial
chromosome
Chromosomes
Microtubules
Intact nuclear
envelope
(b) Dinoflagellates
Kinetochore
microtubule
Intact nuclear
envelope
(c) Diatoms and yeasts
Kinetochore
microtubule
Fragments of
nuclear envelope
(d)

Most eukaryotes

Слайд 53Fig. 12-12ab
Bacterial
chromosome
Chromosomes
Microtubules
(a) Bacteria
(b) Dinoflagellates
Intact nuclear
envelope


Слайд 54Fig. 12-12cd
Kinetochore
microtubule
(c) Diatoms and yeasts
Kinetochore
microtubule
(d) Most eukaryotes
Fragments of
nuclear envelope
Intact nuclear
envelope


Слайд 55Concept 12.3: The eukaryotic cell cycle is regulated by a molecular

control system

The frequency of cell division varies with the type of cell
These cell cycle differences result from regulation at the molecular level

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 56Evidence for Cytoplasmic Signals
The cell cycle appears to be driven by

specific chemical signals present in the cytoplasm
Some evidence for this hypothesis comes from experiments in which cultured mammalian cells at different phases of the cell cycle were fused to form a single cell with two nuclei

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 57Fig. 12-13
Experiment 1
Experiment 2

EXPERIMENT

RESULTS
S
G1
M
G1
M
M
S
S
When a cell in the
S phase was fused


with a cell in G1, the G1
nucleus immediately
entered the S
phase—DNA was
synthesized.

When a cell in the
M phase was fused with
a cell in G1, the G1
nucleus immediately
began mitosis—a
spindle formed and
chromatin condensed,
even though the
chromosome had not
been duplicated.


Слайд 58The 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 clock
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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 59Fig. 12-14
S
G1
M checkpoint
G2
M
Control
system
G1 checkpoint
G2 checkpoint


Слайд 60For many cells, the G1 checkpoint seems to be the most

important one
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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 61Fig. 12-15
G1
G0
G1 checkpoint
Cell receives a go-ahead
signal
G1
(b) Cell does

not receive a
go-ahead signal

Слайд 62The Cell Cycle Clock: Cyclins and Cyclin-Dependent Kinases
Two types of regulatory

proteins are involved in cell cycle control: cyclins and cyclin-dependent kinases (Cdks)
The activity of cyclins and Cdks fluctuates during the cell cycle
MPF (maturation-promoting factor) is a cyclin-Cdk complex that triggers a cell’s passage past the G2 checkpoint into the M phase

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 63Fig. 12-16
Protein kinase activity (– )
% of dividing cells (– )
Time

(min)

300

200

400

100

0

1

2

3

4

5

30

500

0

20

10


RESULTS


Слайд 64Fig. 12-17
M
G1
S
G2
M
G1
S
G2
M
G1
MPF activity
Cyclin
concentration
Time
(a) Fluctuation of MPF activity and cyclin concentration during

the cell cycle

Degraded
cyclin

Cdk

G1

S

G2

M

Cdk

G2

checkpoint

Cyclin is
degraded

Cyclin

MPF

(b) Molecular mechanisms that help regulate the cell cycle

Cyclin accumulation


Слайд 65Fig. 12-17a
Time
(a) Fluctuation of MPF activity and cyclin concentration during

the cell cycle

Cyclin
concentration

MPF activity

M

M

M

S

S

G1

G1

G1

G2

G2


Слайд 66Fig. 12-17b
Cyclin is
degraded
Cdk
MPF
Cdk
M
S
G1
G2
checkpoint
Degraded
cyclin
Cyclin
(b) Molecular mechanisms that help regulate the cell cycle
G2
Cyclin

accumulation

Слайд 67Stop and Go Signs: Internal and External Signals at the Checkpoints
An

example of an internal signal is that kinetochores not attached to spindle microtubules send a molecular signal that delays anaphase
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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 68Fig. 12-18
Petri
plate
Scalpels
Cultured fibroblasts
Without PDGF
cells fail to divide
With PDGF
cells prolifer-
ate
10 µm


Слайд 69Another 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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 70Fig. 12-19
Anchorage dependence
Density-dependent inhibition
Density-dependent inhibition
(a) Normal mammalian cells
(b) Cancer cells
25 µm
25

µm

Слайд 71Cancer cells exhibit neither density-dependent inhibition nor anchorage dependence
Copyright © 2008

Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Слайд 72Loss of Cell Cycle Controls in Cancer Cells
Cancer cells do not

respond normally to the body’s control mechanisms
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

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 73A normal cell is converted to a cancerous cell by a

process called transformation
Cancer cells form tumors, masses of abnormal cells within otherwise normal tissue
If abnormal cells remain 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 secondary tumors

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 74



Fig. 12-20
Tumor
A tumor grows
from a single
cancer cell.
Glandular
tissue
Lymph
vessel
Blood
vessel
Metastatic
tumor
Cancer
cell
Cancer cells
invade neigh-
boring tissue.
Cancer cells

spread
to other parts of
the body.

Cancer cells may
survive and
establish a new
tumor in another
part of the body.

1

2

3

4


Слайд 75Fig. 12-UN1
Telophase and
Cytokinesis
Anaphase
Metaphase
Prometaphase
Prophase
MITOTIC (M) PHASE
Cytokinesis
Mitosis
S
G1
G2
INTERPHASE


Слайд 76Fig. 12-UN2


Слайд 77Fig. 12-UN3


Слайд 78Fig. 12-UN4


Слайд 79Fig. 12-UN5


Слайд 80Fig. 12-UN6


Слайд 81You should now be able to:
Describe the structural organization of the

prokaryotic genome and the eukaryotic genome
List the phases of the cell cycle; describe the sequence of events during each phase
List the phases of mitosis and describe the events characteristic of each phase
Draw or describe the mitotic spindle, including centrosomes, kinetochore microtubules, nonkinetochore microtubules, and asters

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


Слайд 82Compare cytokinesis in animals and plants
Describe the process of binary fission

in bacteria and explain how eukaryotic mitosis may have evolved from binary fission
Explain how the abnormal cell division of cancerous cells escapes normal cell cycle controls
Distinguish between benign, malignant, and metastatic tumors

Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings


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