1. Chapter 12
The Cell Cycle

2. By the end of this chapter you should 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
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3. Compare 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
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4. Overview: The Key Roles of Cell Division
The ability to reproduce best distinguishes living from nonliving.
The continuity of life is based on the reproduction of cells, or cell division
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5. Multicellular organisms depend on cell division for:
In 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 part of the cell cycle, the life of a cell from formation to its own division
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6. (a) Reproduction (b) Growth and development (c) Tissue renewal
Fig. 12-2
100 µm
200 µm
20 µm
(a) Reproduction
(b) Growth and
development
(c) Tissue renewal
Figure 12.2 The functions of cell division
Single-celled Amoeba
dividing into two cells
Sand dollar embryo after
the first division of the
fertilized egg.
Dividing bone marrow cells

7. Most cell division results in daughter cells with identical DNA
Concept 12.1: Cell division results in genetically identical daughter cells
Most cell division results in daughter cells with identical DNA
A special type of division produces nonidentical daughter cells (gametes, or sperm and egg cells)
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8. Cellular 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 (as in prokaryotic cells) or a number of DNA molecules (as in eukaryotic cells)
DNA molecules in a cell are packaged into chromosomes
A typical human cell has 6ft of DNA
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9. Somatic cells (body cells) have two sets of chromosomes
Different species have different numbers of chromosomes. Ex: Humans = 46
Somatic cells (body 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, which is made of DNA and protein
Chromatin condenses during cell division to form chromosomes.
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10. Distribution 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
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11. 0.5 µm Chromosomes DNA molecules Chromo- some arm Chromosome
Fig. 12-4
0.5 µm
Chromosomes
DNA molecules
Chromo-
some arm
Chromosome
duplication
(including DNA
synthesis)
Centromere
Sister
chromatids
Figure 12.4 Chromosome duplication and distribution during cell division
Separation of
sister chromatids
Centromere
Sister chromatids

12. Eukaryotic 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
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13. Concept 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
He discovered that the process of cell division happens in distinct phases.
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14. Phases of the Cell Cycle
The cell cycle consists of
Interphase (cell growth and copying of chromosomes in preparation for cell division)
Mitotic (M) phase (mitosis and cytokinesis)
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
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15. S (DNA synthesis) G1 Cytokinesis G2 Mitosis
Fig. 12-5
INTERPHASE S
(DNA synthesis) G1
Cytokinesis G2
Mitosis
Figure 12.5 The cell cycle
MITOTIC
(M) PHASE

16. Mitosis is conventionally divided into five phases:
Prophase
Prometaphase
Metaphase
Anaphase
Telophase
Cytokinesis is well underway by late telophase
For the Cell Biology Video Myosin and Cytokinesis, go to Animation and Video Files.
BioFlix: Mitosis
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

17. Chromosome, consisting of two sister chromatids
Fig. 12-6
G2 of Interphase
Prophase
Prometaphase
Metaphase
Anaphase
Telophase and Cytokinesis
Centrosomes
(with centriole
pairs)
Chromatin
(duplicated)
Early mitotic
spindle
Aster
Centromere
Fragments
of nuclear
envelope
Nonkinetochore
microtubules
Metaphase
plate
Cleavage
furrow
Nucleolus
forming
Figure 12.6 The mitotic division of an animal cell
Daughter
chromosomes
Nucleolus
Nuclear
envelope
Plasma
membrane
Chromosome, consisting
of two sister chromatids
Kinetochore
Kinetochore
microtubule
Spindle
Centrosome at
one spindle pole
Nuclear
envelope
forming

18. G2 of Interphase Prophase Prometaphase
Fig. 12-6a
Figure 12.6 The mitotic division of an animal cell
G2 of Interphase
Prophase
Prometaphase

19. Chromosome, consisting of two sister chromatids
Fig. 12-6b
G2 of Interphase
Prophase
Prometaphase
Centrosomes
(with centriole
pairs)
Chromatin
(duplicated)
Early mitotic
spindle
Aster
Centromere
Fragments
of nuclear
envelope
Nonkinetochore
microtubules
Figure 12.6 The mitotic division of an animal cell
Nucleolus
Nuclear
envelope
Plasma
membrane
Chromosome, consisting
of two sister chromatids
Kinetochore
Kinetochore
microtubule
Chromatin is duplicated but
not condensed. Centrosomes
& nucleous visible. Nuclear
envelope present
Chromatin condenses into
chromosomes with sister
chromatids visible. Nucleolus
disappears. Mitotic spindle
begins to develop
Nuclear envelope breaks up.
Chromosomes condense more
and have kinetochores which
attach to spindle fibers

20. Telophase and Cytokinesis
Fig. 12-6c
Figure 12.6 The mitotic division of an animal cell
Metaphase
Anaphase
Telophase and Cytokinesis

21. Telophase and Cytokinesis
Fig. 12-6d
Metaphase
Anaphase
Telophase and Cytokinesis
Metaphase
plate
Cleavage
furrow
Nucleolus
forming
Figure 12.6 The mitotic division of an animal cell
Daughter
chromosomes
Nuclear
envelope
forming
Spindle
Centrosome at
one spindle pole
Chromosomes line up in center.
Centrosomes at opposite poles.
Sister chromatids separate
and are pulled to opposite
ends of the cell. Cell begins
to elongate
Two daughter nuclei form
in the cell. Nuclear envelopes
reform and nucleoli reappear.
Chromosomes un-condense.

22. The 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
For the Cell Biology Video Spindle Formation During Mitosis, go to Animation and Video Files.
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

23. An aster (a radial array of short microtubules) extends from each centrosome
The spindle includes the centrosomes, the spindle microtubules, and the asters
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24. During 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

25. Fig. 12-7
Aster
Centrosome
Sister
chromatids
Microtubules
Chromosomes
Metaphase
plate
Kineto-
chores
Centrosome
1 µm
Figure 12.7 The mitotic spindle at metaphase
Overlapping
nonkinetochore
microtubules
Kinetochore
microtubules
0.5 µm

26. The microtubules shorten by depolymerizing at their kinetochore ends
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
For the Cell Biology Video Microtubules in Anaphase, go to Animation and Video Files.
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

27. EXPERIMENT RESULTS CONCLUSION Kinetochore Spindle pole Mark Chromosome
Fig. 12-8
EXPERIMENT
Kinetochore
Spindle
pole
Mark
RESULTS
Figure 12.8 At which end do kinetochore microtubules shorten during anaphase?
CONCLUSION
Chromosome
movement
Kinetochore
Motor
protein
Tubulin
subunits
Microtubule
Chromosome

28. Nonkinetochore 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
For the Cell Biology Video Microtubules in Cell Division, go to Animation and Video Files.
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

29. 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
Animation: Cytokinesis
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

30. Figure 12.9 Cytokinesis in animal and plant cells
Vesicles
forming
cell plate
Wall of
parent cell
1 µm
100 µm
Cleavage furrow
Cell plate
New cell wall
Figure 12.9 Cytokinesis in animal and plant cells
Contractile ring of
microfilaments
Daughter cells
Daughter cells
(a) Cleavage of an animal cell (SEM)
(b) Cell plate formation in a plant cell (TEM)

31. a cell plate at the end, leading to the formation of a new cell wall.
Fig
The same mitotic phases can be seen in plant cells. Note the appearance of
a cell plate at the end, leading to the formation of a new cell wall.
Nucleus
Chromatin
condensing
10 µm
Nucleolus
Chromosomes
Cell plate
Figure Mitosis in a plant cell 1
Prophase 2
Prometaphase 3
Metaphase 4
Anaphase 5
Telophase

32. Binary 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
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33. Cell wall Origin of replication Plasma membrane E. coli cell Bacterial
Fig
Cell wall
Origin of
replication
Plasma
membrane
E. coli cell
Bacterial
chromosome
Two copies
of origin
Figure Bacterial cell division by binary fission

34. Cell wall Origin of replication Plasma membrane E. coli cell Bacterial
Fig
Cell wall
Origin of
replication
Plasma
membrane
E. coli cell
Bacterial
chromosome
Two copies
of origin
Origin
Origin
Figure Bacterial cell division by binary fission

35. Cell wall Origin of replication Plasma membrane E. coli cell Bacterial
Fig
Cell wall
Origin of
replication
Plasma
membrane
E. coli cell
Bacterial
chromosome
Two copies
of origin
Origin
Origin
Figure Bacterial cell division by binary fission

36. Cell wall Origin of replication Plasma membrane E. coli cell Bacterial
Fig
Cell wall
Origin of
replication
Plasma
membrane
E. coli cell
Bacterial
chromosome
Two copies
of origin
Origin
Origin
Figure Bacterial cell division by binary fission

37. The 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 (see diagram)
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38. Origins move to opposite sides and duplicated chromosomes split
Fig
Origins move to opposite
sides and duplicated
chromosomes split
Bacterial
chromosome
(a) Bacteria
Chromosomes
Chromosomes attach to
nuclear envelope; microtubules
pass through nucleus
Microtubules
Intact nuclear
envelope
(b) Dinoflagellates
Kinetochore
microtubule
Microtubules form a spindle
within the nucleus and split
the chromosomes.
Intact nuclear
envelope
Figure A hypothetical sequence for the evolution of mitosis
(c) Diatoms and yeasts
Kinetochore
microtubule
Nucleus disappears; microtubules
form a spindle and separate
chromosomes.
Fragments of
nuclear envelope
(d) Most eukaryotes

39. Concept 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
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
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40. EXPERIMENT RESULTS Experiment 1 Experiment 2 S G1 M G1 S S M M
Fig
EXPERIMENT
Experiment 1
Experiment 2 S G1 M G1
RESULTS S S M M
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.
Figure Do molecular signals in the cytoplasm regulate the cell cycle?

41. 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 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
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42. G1 checkpoint Control system S G1 G2 M M checkpoint G2 checkpoint
Fig
G1 checkpoint
Control
system S G1 G2 M
Figure Mechanical analogy for the cell cycle control system
M checkpoint
G2 checkpoint

43. For 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
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44. Most cells of the human body are actually in the G0 phase. Example:
Mature nerve and muscle cells

45. G0 G1 G1 G1 checkpoint (b) Cell does not receive a go-ahead signal
Fig G0
G1 checkpoint
Figure The G1 checkpoint G1 G1
Cell receives a go-ahead
signal
(b) Cell does not receive a
go-ahead signal

46. The 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
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47. Stop 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
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48. Scalpels Petri plate Without PDGF cells fail to divide With PDGF
Fig
Scalpels
Petri
plate
Without PDGF
cells fail to divide
Figure The effect of a growth factor on cell division
With PDGF
cells prolifer-
ate
Cultured fibroblasts
10 µm

49. 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
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50. Density-dependent inhibition
Fig
Anchorage dependence
Density-dependent inhibition
Density-dependent inhibition
Figure Density-dependent inhibition and anchorage dependence of cell division
25 µm
25 µm
(a) Normal mammalian cells
(b) Cancer cells

51. Cancer cells do not respond normally to the body’s control mechanisms
Cancer cells exhibit neither density-dependent inhibition nor anchorage dependence
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
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52. A 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
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53. G1 S Cytokinesis Mitosis G2 MITOTIC (M) PHASE Prophase Telophase and
Fig. 12-UN1
INTERPHASE G1 S
Cytokinesis
Mitosis G2
MITOTIC (M) PHASE
Prophase
Telophase and
Cytokinesis
Prometaphase
Anaphase
Metaphase

54. Fig. 12-UN2

55. Fig. 12-UN3

56. Fig. 12-UN4

57. Fig. 12-UN5

58. Fig. 12-UN6