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Chapter 12 The Cell Cycle PowerPoint TextEdit Art Slides for Biology, Seventh Edition Neil Campbell and Jane Reece Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.1 Chromosomes in a dividing cell Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.2 The functions of cell division 100 µm (a) Reproduction. An amoeba, a single-celled eukaryote, is dividing into two cells. Each new cell will be an individual organism (LM). 200 µm 20 µm (b) Growth and development. (c) Tissue renewal. These dividing This micrograph shows a bone marrow cells (arrow) will sand dollar embryo shortly after give rise to new blood cells (LM). the fertilized egg divided, forming two cells (LM). Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.3 Eukaryotic chromosomes 50 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.4 Chromosome duplication and distribution during cell division 0.5 µm A eukaryotic cell has multiple chromosomes, one of which is represented here. Before duplication, each chromosome has a single DNA molecule. Once duplicated, a chromosome consists of two sister chromatids connected at the centromere. Each chromatid contains a copy of the DNA molecule. Mechanical processes separate the sister chromatids into two chromosomes and distribute them to two daughter cells. Chromosome duplication (including DNA synthesis) Centromere Separation of sister chromatids Centrometers Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Sister chromatids Sister chromatids Figure 12.5 The cell cycle INTERPHASE S (DNA synthesis) G1 G2 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.6 Exploring The Mitotic Division of an Animal Cell G2 OF INTERPHASE Centrosomes (with centriole pairs) Nucleolus Chromatin (duplicated) Nuclear Plasma envelope membrane PROPHASE Early mitotic spindle Aster Centromere Chromosome, consisting of two sister chromatids Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings PROMETAPHASE Fragments of nuclear envelope Kinetochore Nonkinetochore microtubules Kinetochore microtubule G2 of Interphase • A nuclear envelope bounds the nucleus. • The nucleus contains one or more nucleoli (singular, nucleolus). • Two centrosomes have formed by replication of a single centrosome. • In animal cells, each centrosome features two centrioles. • Chromosomes, duplicated during S phase, cannot be seen individually because they have not yet condensed. The light micrographs show dividing lung cells from a newt, which has 22 chromosomes in its somatic cells (chromosomes appear blue, microtubules green, intermediate filaments red). For simplicity, the drawings show only four chromosomes. Prophase • The chromatin fibers become more tightly coiled, condensing into discrete chromosomes observable with a light microscope. • The nucleoli disappear. • Each duplicated chromosome appears as two identical sister chromatids joined together. • The mitotic spindle begins to form. It is composed of the centrosomes and the microtubules that extend from them. The radial arrays of shorter microtubules that extend from the centrosomes are called asters (“stars”). • The centrosomes move away from each other, apparently propelled by the lengthening microtubules between them. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Prometaphase • The nuclear envelope fragments. • The microtubules of the spindle can now invade the nuclear area and interact with the chromosomes, which have become even more condensed. • Microtubules extend from each centrosome toward the middle of the cell. • Each of the two chromatids of a chromosome now has a kinetochore, a specialized protein structure located at the centromere. • Some of the microtubules attach to the kinetochores, becoming “kinetochore microtubules.” These kinetochore microtubules jerk the chromosomes back and forth. • Nonkinetochore microtubules interact with those from the opposite pole of the spindle. METAPHASE ANAPHASE Metaphase plate Spindle Centrosome at Daughter one spindle pole chromosomes Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings TELOPHASE AND CYTOKINESIS Cleavage furrow Nuclear envelope forming Nucleolus forming Metaphase • Metaphase is the longest stage of mitosis, lasting about 20 minutes. • The centrosomes are now at opposite ends of the cell. •The chromosomes convene on the metaphase plate, an imaginary plane that is equidistant between the spindle’s two poles. The chromosomes’ centromeres lie on the metaphase plate. • For each chromosome, the kinetochores of the sister chromatids are attached to kinetochore microtubules coming from opposite poles. • The entire apparatus of microtubules is called the spindle because of its shape. Anaphase • Anaphase is the shortest stage of mitosis, lasting only a few minutes. • Anaphase begins when the two sister chromatids of each pair suddenly part. Each chromatid thus becomes a fullfledged chromosome. • The two liberated chromosomes begin moving toward opposite ends of the cell, as their kinetochore microtubules shorten. Because these microtubules are attached at the centromere region, the chromosomes move centromere first (at about 1 µm/min). • The cell elongates as the nonkinetochore microtubules lengthen. • By the end of anaphase, the two ends of the cell have equivalent—and complete—collections of chromosomes. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Telophase • Two daughter nuclei begin to form in the cell. • Nuclear envelopes arise from the fragments of the parent cell’s nuclear envelope and other portions of the endomembrane system. • The chromosomes become less condensed. • Mitosis, the division of one nucleus into two genetically identical nuclei, is now complete. Cytokinesis • The division of the cytoplasm is usually well underway by late telophase, so the two daughter cells appear shortly after the end of mitosis. • In animal cells, cytokinesis involves the formation of a cleavage furrow, which pinches the cell in two. Figure 12.7 The mitotic spindle at metaphase Aster Sister chromatids Centrosome Metaphase Plate Kinetochores Overlapping nonkinetochore microtubules Kinetochores microtubules 0.5 µm Microtubules Chromosomes Centrosome 1 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.8 Inquiry During anaphase, do kinetochore microtubules shorten at their spindle pole ends or their kinetochore ends? EXPERIMENT 1 The microtubules of a cell in early anaphase were labeled with a fluorescent dye that glows in the microscope (yellow). Kinetochore Spindle pole Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 2 A Laser was used to mark the kinetochore mircotubles by eliminating the fluorescnce in a region between one spindle pole and the chromosomes. As anaphase proceeded, researches monitored the changes in the lengths of the microtubles on either side of the mark. Mark RESULTS As the chromosomes moved toward the poles, the microtubule segments on the kinetochore side of the laser mark shortened, while those on the spindle pole side stayed the same length. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings CONCLUSION This experiment demonstrated that during anaphase, kinetochore microtubules shorten at their kinetochore ends, not at their spindle pole ends. This is just one of the experiments supporting the hypothesis that during anaphase, a chromosome tracks along a microtubule as the microtubule depolymerizes at its kinetochore end, releasing tubulin subunits Chromosome movement Microtubule Kinetochore Tubulin subunits Motor protein Chromosome Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.9 Cytokinesis in animal and plant cells 100 µm Cleavage furrow Contractile ring of microfilaments Vesicles forming cell plate Wall of patent cell 1 µm Cell plate New cell wall Daughter cells Daughter cells (a) Cleavage of an animal cell (SEM) Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings (b) Cell plate formation in a plant cell (SEM) Figure 12.10 Mitosis in a plant cell Chromatine Nucleus Nucleolus condensing 1 Prophase. The chromatin is condensing. The nucleolus is beginning to disappear. Although not yet visible in the micrograph, the mitotic spindle is staring to from. Chromosome Metaphase. The 2 Prometaphase. 3 4 spindle is complete, We now see discrete and the chromosomes, chromosomes; each attached to microtubules consists of two at their kinetochores, identical sister are all at the metaphase chromatids. Later plate. in prometaphase, the nuclear envelop will fragment. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 5 Anaphase. The chromatids of each chromosome have separated, and the daughter chromosomes are moving to the ends of cell as their kinetochore microtubles shorten. Telophase. Daughter nuclei are forming. Meanwhile, cytokinesis has started: The cell plate, which will divided the cytoplasm in two, is growing toward the perimeter of the parent cell. Figure 12.11 Bacterial cell division (binary fission) Origin of replication Cell wall Plasma Membrane E. coli cell 1 Chromosome replication begins. Soon thereafter, one copy of the origin moves rapidly toward the other end of the cell. 2 Replication continues. One copy of the origin is now at each end of the cell. 3 Replication finishes. The plasma membrane grows inward, and new cell wall is deposited. 4 Two daughter cells result. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Two copies of origin Origin Bacterial Chromosome Origin Figure 12.12 A hypothetical sequence for the evolution of mitosis (a) Prokaryotes. During binary fission, the origins of the daughter chromosomes move to opposite ends of the cell. The mechanism is not fully understood, but proteins may anchor the daughter chromosomes to specific sites on the plasma membrane. (b) Dinoflagellates. In unicellular protists called dinoflagellates, the nuclear envelope remains intact during cell division, and the chromosomes attach to the nuclear envelope. Microtubules pass through the nucleus inside cytoplasmic tunnels, reinforcing the spatial orientation of the nucleus, which then divides in a fission process reminiscent of bacterial division. (c) Diatoms. In another group of unicellular protists, the diatoms, the nuclear envelope also remains intact during cell division. But in these organisms, the microtubules form a spindle within the nucleus. Microtubules separate the chromosomes, and the nucleus splits into two daughter nuclei. (d) Most eukaryotes. In most other eukaryotes, including plants and animals, the spindle forms outside the nucleus, and the nuclear envelope breaks down during mitosis. Microtubules separate the chromosomes, and the nuclear envelope then re-forms. Bacterial chromosome Chromosomes Microtubules Intact nuclear envelope Kinetochore microtubules Intact nuclear envelope Kinetochore microtubules Centrosome Fragments of nuclear envelope Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.13 Inquiry Are there molecular signals in the cytoplasm that regulate the cell cycle? EXPERIMENTS In each experiment, cultured mammalian cells at two different phases of the cell cycle were induced to fuse. Experiment 1 S Experiment 2 G1 M S M G1 RESULTS S When a cell in the S phase was fused with a cell in G1, the G1 cell immediately entered the S phase—DNA was synthesized. CONCLUSION M When a cell in the M phase was fused with a cell in G1, the G1 cell immediately began mitosis— a spindle formed and chromatin condensed, even though the chromosome had not been duplicated. The results of fusing cells at two different phases of the cell cycle suggest that molecules present in the cytoplasm of cells in the S or M phase control the progression of phases. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.14 Mechanical analogy for the cell cycle control system G1 checkpoint Control system G1 M M checkpoint G2 checkpoint Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings G2 S Figure 12.15 The G1 checkpoint G0 G1 checkpoint G1 (a) If a cell receives a go-ahead signal at the G1 checkpoint, the cell continues on in the cell cycle. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings G1 (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. (a) Fluctuation of MPF activity and cyclin concentration during the cell cycle Relative Concentration Figure 12.16 Molecular control of the cell cycle at the G2 checkpoint G1 S G2 M MPF activity G 1 S G2 M Cyclin Time (b) Molecular mechanisms that help regulate the cell cycle 1 Synthesis of cyclin begins in late S phase and continues through G2. Because cyclin is protected from degradation during this stage, it accumulates. 5 During G1, conditions in the cell favor degradation of cyclin, and the Cdk component of MPF is recycled. Cdk Degraded Cyclin Cyclin is degraded 4 During anaphase, the cyclin component of MPF is degraded, terminating the M phase. The cell enters the G1 phase. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings G2 Cdk checkpoint MPF Cyclin 2 Accumulated cyclin molecules combine with recycled Cdk molecules, producing enough molecules of MPF to pass the G2 checkpoint and initiate the events of mitosis. 3 MPF promotes mitosis by phosphorylating various proteins. MPF‘s activity peaks during metaphase. Figure 12.17 Inquiry Does platelet-derived growth factor (PDGF) stimulate the division of human fibroblast cells in culture? EXPERIMENT 1 Scalpels A sample of connective tissue was cut up into small pieces. Petri plate 2 Enzymes were used to digest the extracellular matrix, resulting in a suspension of free fibroblast cells. 3 Cells were transferred to sterile culture vessels containing a basic growth medium consisting of glucose, amino acids, salts, and antibiotics (as a precaution against bacterial growth). PDGF was added to half the vessels. The culture vessels were incubated at 37°C. With PDGF Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Without PDGF RESULTS a In a basic growth medium without PDGF (the control), cells failed to divide. Without PDGF b In a basic growth medium plus PDGF, cells proliferated. The SEM shows cultured fibroblasts. With PDGF 10 µm CONCLUSION This experiment confirmed that PDGF stimulates the division of human fibroblast cells in culture. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.18 Density-dependent inhibition and anchorage dependence of cell division (a) Normal mammalian cells. The availability of nutrients, growth factors, and a substratum for attachment limits cell density to a single layer. Cells anchor to dish surface and divide (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 (density-dependent inhibition). 25 µm Cancer cells do not exhibit anchorage dependence or density-dependent inhibition. (b) Cancer cells. Cancer cells usually continue to divide well beyond a single layer, forming a clump of overlapping cells. 25 µm Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Figure 12.19 The growth and metastasis of a malignant breast tumor Lymph vessel Tumor Blood vessel Glandular tissue 1 A tumor grows from a single cancer cell. 2 Cancer cells invade neighboring tissue. Cancer cell 3 Cancer cells spread through lymph and blood vessels to other parts of the body. Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Metastatic Tumor 4 A small percentage of cancer cells may survive and establish a new tumor in another part of the body. Unnumbered Figure p. 235 Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings 1. Using the data in the table below, the best conclusion concerning the difference between the S phases for beta and gamma is that Minutes Spent in Cell Cycle Phases Cell Type G1 S G M 2 Beta Delta 18 24 12 16 100 0 0 0 Gamma 18 48 14 20 a. gamma contains more DNA than beta. b. beta and gamma contain the same amount of DNA. c. beta contains more RNA than gamma. d. gamma contains 48 times more DNA and RNA than beta. e. beta is a plant cell and gamma is an animal cell. Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 2. Cytokinesis usually, but not always, follows mitosis. If a cell completed mitosis but not cytokinesis, what would be the result? a. a cell with a single large nucleus b. a cell with high concentrations of actin and myosin c. a cell with two abnormally small nuclei d. a cell with two nuclei e. a cell with two nuclei but with half the amount of DNA Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 3. Taxol is an anticancer drug extracted from the Pacific yew tree. In animal cells, taxol disrupts microtubule formation by binding to microtubules and accelerating their assembly from the protein precursor, tubulin. Surprisingly, this stops mitosis. Specifically, taxol must affect a. the fibers of the mitotic spindle. b. anaphase. c. formation of the centrioles. d. chromatid assembly. e. the S phase of the cell cycle. Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 4. Movement of the chromosomes during anaphase would be most affected by a drug that a. reduced cyclin concentrations. b. increased cyclin concentrations. c. prevented elongation of microtubules. d. prevented shortening of microtubules. e. prevented attachment of the microtubules to the kinetochore. Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 5. Measurements of the amount of DNA per nucleus were taken on a large number of cells from a growing fungus. The measured DNA levels ranged from 3 to 6 picograms per nucleus. In which stage of the cell cycle was the nucleus with 6 picograms of DNA? a. G0 b. G1 c. S d. G2 e. M Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 6. A group of cells is assayed for DNA content immediately following mitosis and is found to have an average of 8 picograms of DNA per nucleus. Those cells would have __________ picograms at the end of the S phase and __________ picograms at the end of G2. a. 8 ... 8 b. 8 ... 16 c. 16 ... 8 d. 16 ... 16 e. 12 ... 16 Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 7. A particular cell has half as much DNA as some of the other cells in a mitotically active tissue. The cell in question is most likely in a. G1. b. G2. c. prophase. d. metaphase. e. anaphase. Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 8. In some organisms, mitosis occurs without cytokinesis occurring. This will result in a. cells with more than one nucleus. b. cells that are unusually small. c. cells lacking nuclei. d. destruction of chromosomes. e. cell cycles lacking an S phase. Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 10. The rhythmic changes in cyclin concentration in a cell cycle are due to a. its increased production once the restriction point is passed. b. the cascade of increased production once its enzyme is phosphorylated by MPF. c. its degradation, which is initiated by active MPF. d. the correlation of its production with the production of Cdk. e. the binding of the growth factor PDGF. Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings 11. A cell in which of the following phases would have the least amount of DNA? a. G0 b. G2 c. prophase d. metaphase e. anaphase Copyright © 2004 Pearson Education, Inc. publishing as Benjamin Cummings