chapter 12 the cell cycle lab 3 mitosis and meiosis
TRANSCRIPT
Chapter 12Chapter 12The Cell CycleThe Cell Cycle
Lab 3
Mitosis and Meiosis
MitosisMitosis
Division of the cell nucleus.
Division of the cell nucleus.
CytokinesisCytokinesis
Division of the cell cytoplasm.
Division of the cell cytoplasm.
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The Cell Cycle
The continuity of life
Is based upon the reproduction of cells, or cell division
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The Cell Cycle – Making an “EXACT copy” Unicellular organisms
Reproduce by cell division
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The Cell Cycle Multicellular organisms depend on cell division for
Development from a fertilized cell
Growth
Repair
Growth and development Tissue renewal
Cell DivisionCell Division Cell division results in genetically
identical daughter cells Cells duplicate their total genetic material
(genome) Before they divide, ensuring that each
daughter cell receives an exact copy of the genetic material, DNA
Cell division results in genetically identical daughter cells
Cells duplicate their total genetic material (genome) Before they divide, ensuring that each
daughter cell receives an exact copy of the genetic material, DNA
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Genetic Material
The DNA molecules in a cell
Are packaged into chromosomes
50 µm
Genetic MaterialGenetic Material
Eukaryotic chromosomes Consist of chromatin, a complex of DNA &
protein that condenses during cell division In animals
Somatic cells have two sets of chromosomes46 in humans
Gametes (egg & sperm) have one set of chromosomes23 in humans
Eukaryotic chromosomes Consist of chromatin, a complex of DNA &
protein that condenses during cell division In animals
Somatic cells have two sets of chromosomes46 in humans
Gametes (egg & sperm) have one set of chromosomes23 in humans
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DNA Replication Each duplicated
chromosome
Has two sister chromatids, which separate during cell division
They are attached by a central area called the centromere
0.5 µm
Chromosomeduplication(including DNA synthesis)
Separation of sister
chromatids
chromatids
centromere
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Phases of the Cell Cycle
The cell cycle consists of
Interphase
Mitotic phase
INTERPHASE
G1
S(DNA synthesis)
G2Cyto
kines
is
Mito
sis
MITOTIC(M) PHASE
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Mitotic Phase
Mitosis consists of five distinct phases
1.) Prophase
2.) Prometaphase
G2 OF INTERPHASE
PROPHASE PROMETAPHASE
Centrosomes(with centriole pairs) Chromatin
(duplicated)
Early mitoticspindle
Aster
CentromereFragmentsof nuclearenvelope
Kinetochore
Nucleolus Nuclearenvelope
Plasmamembrane
Chromosome, consistingof two sister chromatids
Kinetochore microtubule
Nonkinetochoremicrotubules
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Mitotic Phase
3.) Metaphase
4.) Anaphase
5.) Telophase (usually followed by cytokinesis)
Centrosome at one spindle pole
Daughter chromosomes
METAPHASE ANAPHASE TELOPHASE AND CYTOKINESIS
Spindle
Metaphaseplate Nucleolus
forming
Cleavagefurrow
Nuclear envelopeforming
Types of MicrotubulesTypes of MicrotubulesKinetochore microtubules
Attach to the kinetochores of chromosomes and move the chromosomes to the metaphase plate
Nonkinetechore microtubules from opposite poles Overlap and push against each other,
elongating the cell
Kinetochore microtubules Attach to the kinetochores of
chromosomes and move the chromosomes to the metaphase plate
Nonkinetechore microtubules from opposite poles Overlap and push against each other,
elongating the cell
Assembly of the spindle microtubules starts in the centrosome. The centrosome (microtubule-organizing
center) of animals has a pair of centrioles at the center, but the function of the centrioles is somewhat undefined.
Assembly of the spindle microtubules starts in the centrosome. The centrosome (microtubule-organizing
center) of animals has a pair of centrioles at the center, but the function of the centrioles is somewhat undefined.
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As mitosis starts, the two centrosomes are located near the nucleus.
As the spindle fibers grow from them, the centrioles are pushed apart.
By the end of prometaphase they develop as the spindle poles at opposite ends of the cell.
As mitosis starts, the two centrosomes are located near the nucleus.
As the spindle fibers grow from them, the centrioles are pushed apart.
By the end of prometaphase they develop as the spindle poles at opposite ends of the cell.
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Each sister chromatid has a kinetochore of proteins and chromosomal DNA at the centromere.
The kinetochores of the joined sister chromatids face in opposite directions.
During prometaphase, some spindle microtubules attach to thekinetochores.
Each sister chromatid has a kinetochore of proteins and chromosomal DNA at the centromere.
The kinetochores of the joined sister chromatids face in opposite directions.
During prometaphase, some spindle microtubules attach to thekinetochores.
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When a chromosome’s kinetochore is “captured” by microtubules, the chromosome moves toward the pole from which those microtubules come.
When microtubules attach to the other pole, this movement stops and a tug-of-war ensues.
Eventually, the chromosome settles midway between the two poles of the cell, the metaphase plate.
Other microtubules from opposite poles interact as well, elongating the cell.
When a chromosome’s kinetochore is “captured” by microtubules, the chromosome moves toward the pole from which those microtubules come.
When microtubules attach to the other pole, this movement stops and a tug-of-war ensues.
Eventually, the chromosome settles midway between the two poles of the cell, the metaphase plate.
Other microtubules from opposite poles interact as well, elongating the cell.
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One hypothesis for the movement of chromosomes in anaphase is that motor proteins at the kinetochore “walk” the attached chromosome along the microtubule toward the opposite pole. The excess microtubule sections
depolymerize.
One hypothesis for the movement of chromosomes in anaphase is that motor proteins at the kinetochore “walk” the attached chromosome along the microtubule toward the opposite pole. The excess microtubule sections
depolymerize.
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Fig. 12.7a
Experiments support the hypothesis that spindle fibers shorten during anaphase from the end attached to the chromosome, not the centrosome.
Experiments support the hypothesis that spindle fibers shorten during anaphase from the end attached to the chromosome, not the centrosome.
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Fig. 12.7b
Nonkinetichore microtubules are responsible for lengthening the cell along the axis defined by the poles. These microtubules interdigitate across the
metaphase plate. During anaphase motor proteins push
microtubules from opposite sides away from each other.
At the same time, the addition of new tubulin monomers extends their length.
Nonkinetichore microtubules are responsible for lengthening the cell along the axis defined by the poles. These microtubules interdigitate across the
metaphase plate. During anaphase motor proteins push
microtubules from opposite sides away from each other.
At the same time, the addition of new tubulin monomers extends their length.
Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
Cytokinesis
In animal cells
Cytokinesis occurs by a process known as cleavage, forming a cleavage furrow
Cleavage furrow
Contractile ring of microfilaments
Daughter cells
100 µm
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Cytokinesis
In plant cells, during cytokinesis
A cell plate forms
Daughter cells
1 µmVesiclesforming cell plate
Wall of patent cell Cell plateNew cell wall
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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
Control system
G2 checkpoint
M checkpoint
G1 checkpoint
G1
S
G2M
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Cell Cycle Control System
The clock has specific checkpoints Where the cell cycle stops until a go-ahead signal is
received
G1 checkpoint
G1G1
G0
(a) If a cell receives a go-ahead signal at the G1 checkpoint, the cell continues on in the cell cycle.
(b) If a cell does not receive a go-ahead signal at the G1checkpoint, the cell exits the cell cycle and goes into G0, a nondividing state.
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Normal Cell Behavior
In density-dependent inhibition
Crowded cells stop dividing
Most animal cells exhibit anchorage dependence
In which they must be attached to a substratum to divide
Cells anchor to dish surface anddivide (anchorage dependence)
When cells have formed a complete single layer, they stop dividing (density-dependent inhibition)
If some cells are scraped away, the remaining cells divide to fill the gap and then stop
25 µm
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Abnormal Cell Behavior
Cancer cells
Transformation is the process of a normal cell becoming cancerous
Cancer cells exhibit neither density-dependent inhibition nor anchorage dependence
Why cells transform is often a mystery but most likely genes controlling the cell control system are involved
25 µm
Cancer cells. Cancer cells usually continue to divide well beyond a single layer, forming a clump of overlapping cells.
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Cancerous Cells
Malignant tumors invade surrounding tissues and can metastasize
Exporting cancer cells to other parts of the body where they may form secondary tumors
Cancer cells invade neighboring tissue.
2 A small percentage of cancer cells may survive and establish a new tumor in another part of the body.
4Cancer cells spread through lymph and blood vessels to other parts of the body.
3A tumor grows from a single cancer cell.
1
Tumor
Glandulartissue
Cancer cell
Bloodvessel
Lymphvessel
MetastaticTumor
Thinking QuestionThinking Question
Many cancer drugs (chemotherapy) work by interfering with the production or proper function of microtubules. What specific effect would this have on cell division and why is this beneficial in the treatment of cancer? Common side effects of chemotherapy are hair loss and nausea. Why do you think this is the case?
Many cancer drugs (chemotherapy) work by interfering with the production or proper function of microtubules. What specific effect would this have on cell division and why is this beneficial in the treatment of cancer? Common side effects of chemotherapy are hair loss and nausea. Why do you think this is the case?
Key Points of Chapter 12Key Points of Chapter 12
Cell division results in two genetically identical daughter cells
The mitotic phase alternates with interphase in the cell cycle
The cell cycle is regulated by a molecular control system
Cell division results in two genetically identical daughter cells
The mitotic phase alternates with interphase in the cell cycle
The cell cycle is regulated by a molecular control system