Ch.12The Cell Cycle

Total Page:16

File Type:pdf, Size:1020Kb

Ch.12The Cell Cycle 100 µm 200 µm 20 µm (a) Reproduction (b) Growth and (c) Tissue renewal development 1 20 µm 2 0.5 µm Chromosomes DNA molecules Chromo- Chromosome some arm duplication (including DNA synthesis) Centromere Sister chromatids Separation of sister chromatids Centromere Sister chromatids 3 G S 1 (DNA synthesis) G2 4 G2 of Interphase Prophase Prometaphase Metaphase Anaphase Telophase and Cytokinesis Centrosomes Chromatin Early mitotic Aster Centromere Fragments Nonkinetochore Metaphase Cleavage Nucleolus (with centriole (duplicated) spindle of nuclear microtubules plate furrow forming pairs) envelope Daughter Nuclear Nucleolus Nuclear Plasma Chromosome, consisting Kinetochore Kinetochore Spindle Centrosome at chromosomes one spindle pole envelope envelope membrane of two sister chromatids microtubule forming 5 Aster Centrosome Sister chromatids Microtubules Chromosomes Metaphase plate Kineto- chores Centrosome 1 µm Overlapping nonkinetochore Kinetochore microtubules microtubules 0.5 µm 6 EXPERIMENT Kinetochore Spindle pole Mark RESULTS CONCLUSION Chromosome movement Kinetochore Motor Tubulin Microtubule protein subunits Chromosome 7 Vesicles Wall of 1 µm 100 µm forming parent cell Cleavage furrow cell plate Cell plate New cell wall Contractile ring of Daughter cells microfilaments Daughter cells (a) Cleavage of an animal cell (SEM) (b) Cell plate formation in a plant cell (TEM) 8 Nucleus Chromatin 10 µm Nucleolus condensing Chromosomes Cell plate 1 Prophase 2 Prometaphase 3 Metaphase 4 Anaphase 5 Telophase 9 Cell wall Origin of replication Plasma membrane E. coli cell Bacterial Two copies chromosome of origin Origin Origin 10 Bacterial chromosome (a) Bacteria 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 11 EXPERIMENT Experiment 1 Experiment 2 S G1 M G1 RESULTS S S M M When a cell in the When a cell in the S phase was fused M phase was fused with with a cell in G1, the G1 a cell in G1, the G1 nucleus immediately nucleus immediately entered the S began mitosis—a phase—DNA was spindle formed and synthesized. chromatin condensed, even though the chromosome had not been duplicated. 12 G1 checkpoint Control system S G1 M G2 M checkpoint G2 checkpoint 13 G0 G1 checkpoint G1 G1 (a) Cell receives a go-ahead (b) Cell does not receive a signal go-ahead signal 14 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 Cyclin accumulation Cyclin Cdk Degraded cyclin G2 Cdk Cyclin is checkpoint degraded Cyclin MPF (b) Molecular mechanisms that help regulate the cell cycle 15 Scalpels Petri plate Without PDGF With PDGF cells fail to divide cells prolifer- ate Cultured fibroblasts 10 µm 16 Anchorage dependence Density-dependent inhibition Density-dependent inhibition 25 µm 25 µm (a) Normal mammalian cells (b) Cancer cells 17 Lymph vessel Tumor Blood vessel Cancer Glandular cell tissue Metastatic tumor 1 A tumor grows 2 Cancer cells 3 Cancer cells spread 4 Cancer cells may from a single invade neigh- to other parts of survive and cancer cell. boring tissue. the body. establish a new tumor in another part of the body. 18 .
Recommended publications
  • RASSF1A Interacts with and Activates the Mitotic Kinase Aurora-A
    Oncogene (2008) 27, 6175–6186 & 2008 Macmillan Publishers Limited All rights reserved 0950-9232/08 $32.00 www.nature.com/onc ORIGINAL ARTICLE RASSF1A interacts with and activates the mitotic kinase Aurora-A L Liu1, C Guo1, R Dammann2, S Tommasi1 and GP Pfeifer1 1Division of Biology, Beckman Research Institute, City of Hope Cancer Center, Duarte, CA, USA and 2Institute of Genetics, University of Giessen, Giessen, Germany The RAS association domain family 1A (RASSF1A) gene tumorigenesis and carcinogen-induced tumorigenesis is located at chromosome 3p21.3 within a specific area of (Tommasi et al., 2005; van der Weyden et al., 2005), common heterozygous and homozygous deletions. RASS- supporting the notion that RASSF1A is a bona fide F1A frequently undergoes promoter methylation-asso- tumor suppressor. However, it is not fully understood ciated inactivation in human cancers. Rassf1aÀ/À mice how RASSF1A is involved in tumor suppression. are prone to both spontaneous and carcinogen-induced The biochemical function of the RASSF1A protein is tumorigenesis, supporting the notion that RASSF1A is a largely unknown. The homology of RASSF1A with the tumor suppressor. However, it is not fully understood how mammalian Ras effector novel Ras effector (NORE)1 RASSF1A is involved in tumor suppression pathways. suggests that the RASSF1A gene product may function Here we show that overexpression of RASSF1A inhibits in signal transduction pathways involving Ras-like centrosome separation. RASSF1A interacts with Aurora-A, proteins. However, recent data indicate that RASSF1A a mitotic kinase. Surprisingly, knockdown of RASS- itself binds to RAS only weakly and that binding to F1A by siRNA led to reduced activation of Aurora-A, RAS may require heterodimerization of RASSF1A and whereas overexpression of RASSF1A resulted in in- NORE1 (Ortiz-Vega et al., 2002).
    [Show full text]
  • GENETICS and GENOMICS Ed
    GENETICS AND GENOMICS Ed. Csaba Szalai, PhD GENETICS AND GENOMICS Editor: Csaba Szalai, PhD, university professor Authors: Chapter 1: Valéria László Chapter 2, 3, 4, 6, 7: Sára Tóth Chapter 5: Erna Pap Chapter 8, 9, 10, 11, 12, 13, 14: Csaba Szalai Chapter 15: András Falus and Ferenc Oberfrank Keywords: Mitosis, meiosis, mutations, cytogenetics, epigenetics, Mendelian inheritance, genetics of sex, developmental genetics, stem cell biology, oncogenetics, immunogenetics, human genomics, genomics of complex diseases, genomic methods, population genetics, evolution genetics, pharmacogenomics, nutrigenetics, gene environmental interaction, systems biology, bioethics. Summary The book contains the substance of the lectures and partly of the practices of the subject of ‘Genetics and Genomics’ held in Semmelweis University for medical, pharmacological and dental students. The book does not contain basic genetics and molecular biology, but rather topics from human genetics mainly from medical point of views. Some of the 15 chapters deal with medical genetics, but the chapters also introduce to the basic knowledge of cell division, cytogenetics, epigenetics, developmental genetics, stem cell biology, oncogenetics, immunogenetics, population genetics, evolution genetics, nutrigenetics, and to a relative new subject, the human genomics and its applications for the study of the genomic background of complex diseases, pharmacogenomics and for the investigation of the genome environmental interactions. As genomics belongs to sytems biology, a chapter introduces to basic terms of systems biology, and concentrating on diseases, some examples of the application and utilization of this scientific field are also be shown. The modern human genetics can also be associated with several ethical, social and legal issues. The last chapter of this book deals with these issues.
    [Show full text]
  • Chromatid Cohesion During Mitosis: Lessons from Meiosis
    Journal of Cell Science 112, 2607-2613 (1999) 2607 Printed in Great Britain © The Company of Biologists Limited 1999 JCS0467 COMMENTARY Chromatid cohesion during mitosis: lessons from meiosis Conly L. Rieder1,2,3 and Richard Cole1 1Wadsworth Center, New York State Dept of Health, PO Box 509, Albany, New York 12201-0509, USA 2Department of Biomedical Sciences, State University of New York, Albany, New York 12222, USA 3Marine Biology Laboratory, Woods Hole, MA 02543-1015, USA *Author for correspondence (e-mail: [email protected]) Published on WWW 21 July 1999 SUMMARY The equal distribution of chromosomes during mitosis and temporally separated under various conditions. Finally, we meiosis is dependent on the maintenance of sister demonstrate that in the absence of a centromeric tether, chromatid cohesion. In this commentary we review the arm cohesion is sufficient to maintain chromatid cohesion evidence that, during meiosis, the mechanism underlying during prometaphase of mitosis. This finding provides a the cohesion of chromatids along their arms is different straightforward explanation for why mutants in proteins from that responsible for cohesion in the centromere responsible for centromeric cohesion in Drosophila (e.g. region. We then argue that the chromatids on a mitotic ord, mei-s332) disrupt meiosis but not mitosis. chromosome are also tethered along their arms and in the centromere by different mechanisms, and that the Key words: Sister-chromatid cohesion, Mitosis, Meiosis, Anaphase functional action of these two mechanisms can be onset INTRODUCTION (related to the fission yeast Cut1P; Ciosk et al., 1998). When Pds1 is destroyed Esp1 is liberated, and this event somehow The equal distribution of chromosomes during mitosis is induces a class of ‘glue’ proteins, called cohesins (e.g.
    [Show full text]
  • Written Response #5
    Written Response #5 • Draw and fill in the chart below about three different types of cells: Written Response #6-18 • In this true/false activity: • You and your partner will discuss the question, each of you will record your response and share your answer with the class. Be prepared to justify your answer. • You are allow to search answers. • You will be limited to 20 seconds per question. Written Response #6-18 6. The water-hating hydrophobic tails of the phospholipid bilayer face the outside of the cell membrane. 7. The cytoplasm essentially acts as a “skeleton” inside the cell. 8. Plant cells have special structures that are not found in animal cells, including a cell wall, a large central vacuole, and plastids. 9. Centrioles help organize chromosomes before cell division. 10. Ribosomes can be found attached to the endoplasmic reticulum. Written Response #6-18 11. ATP is made in the mitochondria. 12. Many of the biochemical reactions of the cell occur in the cytoplasm. 13. Animal cells have chloroplasts, organelles that capture light energy from the sun and use it to make food. 14. Small hydrophobic molecules can easily pass through the plasma membrane. 15. In cell-level organization, cells are not specialized for different functions. Written Response #6-18 16. Mitochondria contains its own DNA. 17. The plasma membrane is a single phospholipid layer that supports and protects a cell and controls what enters and leaves it. 18. The cytoskeleton is made from thread-like filaments and tubules. 3.2 HW 1. Describe the composition of the plasma membrane.
    [Show full text]
  • Mitosis Vs. Meiosis
    Mitosis vs. Meiosis In order for organisms to continue growing and/or replace cells that are dead or beyond repair, cells must replicate, or make identical copies of themselves. In order to do this and maintain the proper number of chromosomes, the cells of eukaryotes must undergo mitosis to divide up their DNA. The dividing of the DNA ensures that both the “old” cell (parent cell) and the “new” cells (daughter cells) have the same genetic makeup and both will be diploid, or containing the same number of chromosomes as the parent cell. For reproduction of an organism to occur, the original parent cell will undergo Meiosis to create 4 new daughter cells with a slightly different genetic makeup in order to ensure genetic diversity when fertilization occurs. The four daughter cells will be haploid, or containing half the number of chromosomes as the parent cell. The difference between the two processes is that mitosis occurs in non-reproductive cells, or somatic cells, and meiosis occurs in the cells that participate in sexual reproduction, or germ cells. The Somatic Cell Cycle (Mitosis) The somatic cell cycle consists of 3 phases: interphase, m phase, and cytokinesis. 1. Interphase: Interphase is considered the non-dividing phase of the cell cycle. It is not a part of the actual process of mitosis, but it readies the cell for mitosis. It is made up of 3 sub-phases: • G1 Phase: In G1, the cell is growing. In most organisms, the majority of the cell’s life span is spent in G1. • S Phase: In each human somatic cell, there are 23 pairs of chromosomes; one chromosome comes from the mother and one comes from the father.
    [Show full text]
  • Questions in Cell Biology
    Name: Questions in Cell Biology Directions: The following questions are taken from previous IB Final Papers on the subject of cell biology. Answer all questions. This will serve as a study guide for the next quiz on Monday 11/21. 1. Outline the process of endocytosis. (Total 5 marks) 2. Draw a labelled diagram of the fluid mosaic model of the plasma membrane. (Total 5 marks) 3. The drawing below shows the structure of a virus. II I 10 nm (a) Identify structures labelled I and II. I: ...................................................................................................................................... II: ...................................................................................................................................... (2) (b) Use the scale bar to calculate the maximum diameter of the virus. Show your working. Answer: ..................................................... (2) (c) Explain briefly why antibiotics are effective against bacteria but not viruses. ............................................................................................................................................... ............................................................................................................................................... ............................................................................................................................................... ..............................................................................................................................................
    [Show full text]
  • Cell Division- Ch 5
    Cell Division- Mitosis and Meiosis When do cells divide? Cell size . One of most important factors affecting size of the cell is size of cell membrane . Cell must remain relatively small to survive (why?) – Cell membrane has to be big enough to take in nutrients and eliminate wastes – As cells get bigger, the volume increases faster than the surface area – Small cells have a larger surface area to volume ratio than larger cells to help with nutrient intake and waste elimination . When a cell reaches its max size, the nucleus starts cell division: called MITOSIS or MEIOSIS Mitosis . General Information – Occurs in somatic (body) cells ONLY!! – Nickname: called “normal” cell division – Produces somatic cells only . Background Info – Starts with somatic cell in DIPLOID (2n) state . Cell contains homologous chromosomes- chromosomes that control the same traits but not necessarily in the same way . 1 set from mom and 1 set from dad – Ends in diploid (2n) state as SOMATIC cells – Goes through one set of divisions – Start with 1 cell and end with 2 cells Mitosis (cont.) . Accounts for three essential life processes – Growth . Result of cell producing new cells . Develop specialized shapes/functions in a process called differentiation . Rate of cell division controlled by GH (Growth Hormone) which is produced in the pituitary gland . Ex. Nerve cell, intestinal cell, etc. – Repair . Cell regenerates at the site of injury . Ex. Skin (replaced every 28 days), blood vessels, bone Mitosis (cont.) – Reproduction . Asexual – Offspring produced by only one parent – Produce offspring that are genetically identical – MITOSIS – Ex. Bacteria, fungi, certain plants and animals .
    [Show full text]
  • Overview of Meiosis
    Sexual Reproduction and Meiosis Chapter 11 Overview of Meiosis Meiosis is a form of cell division that leads to the production of gametes. gametes: egg cells and sperm cells -contain half the number of chromosomes of an adult body cell Adult body cells (somatic cells) are diploid, containing 2 sets of chromosomes. Gametes are haploid, containing only 1 set of chromosomes. 2 Overview of Meiosis Sexual reproduction includes the fusion of gametes (fertilization) to produce a diploid zygote. Life cycles of sexually reproducing organisms involve the alternation of haploid and diploid stages. Some life cycles include longer diploid phases, some include longer haploid phases. 3 1 4 5 6 2 7 Features of Meiosis Meiosis includes two rounds of division – meiosis I and meiosis II. During meiosis I, homologous chromosomes (homologues) become closely associated with each other. This is synapsis. Proteins between the homologues hold them in a synaptonemal complex. 8 9 3 Features of Meiosis Crossing over: genetic recombination between non-sister chromatids -physical exchange of regions of the chromatids chiasmata: sites of crossing over The homologues are separated from each other in anaphase I. 10 Features of Meiosis Meiosis involves two successive cell divisions with no replication of genetic material between them. This results in a reduction of the chromosome number from diploid to haploid. 11 12 4 The Process of Meiosis Prophase I: -chromosomes coil tighter -nuclear envelope dissolves -homologues become closely associated in synapsis -crossing over
    [Show full text]
  • The Kinase Activity of Aurora B Is Required for Kinetochore-Microtubule Interactions During Mitosis
    Current Biology, Vol. 12, 894–899, June 4, 2002, 2002 Elsevier Science Ltd. All rights reserved. PII S0960-9822(02)00848-5 The Kinase Activity of Aurora B Is Required for Kinetochore-Microtubule Interactions during Mitosis Maki Murata-Hori and Yu-li Wang1 chromosomal congression, we monitored the move- Department of Physiology ment of individual centromeres in cells expressing a high University of Massachusetts Medical School level of aurora B(K-R)-GFP or control cells expressing a Worcester, Massachusetts 01605 similar level of wild-type aurora B-GFP (Figure 1B). Both aurora B-GFP and aurora B(K-R)-GFP were localized at centromeres and spindle poles [6] and to a less extent Summary along chromosomal arms (see Figures 3A and 3D). In control cells, the centromeres of neighboring chro- As a component of the “chromosomal passenger pro- mosomes moved independently of each other at an av- Ϯ ␮ Ϯ ϭ tein complex,” the aurora B kinase is associated with erage rate of 1.8 1.2 m/min (mean SD, n 22), centromeres during prometaphase and with midzone with frequent changes in direction (Figure 1B, left). They ف microtubules during anaphase and is required for both eventually accumulated at the metaphase plate 20 min mitosis and cytokinesis [1–6]. Ablation of aurora B after nuclear envelope breakdown (19/19, Figures 1Aa– causes defects in both prometaphase chromosomal 1Ad; Supplementary Movie 1 available with this article congression and the spindle checkpoint [4–6]; how- online). In contrast, in cells expressing aurora B(K-R)- ever, the mechanisms underlying these defects are GFP, centromeres of neighboring chromosomes moved Ϯ ␮ unclear.
    [Show full text]
  • Ran Controls Microtubule Asters and Nuclear Assembly 2455 Chromatin Rounded up (Fig
    Journal of Cell Science 112, 2453-2461 (1999) 2453 Printed in Great Britain © The Company of Biologists Limited 1999 JCS0524 Ran-GTP stabilises microtubule asters and inhibits nuclear assembly in Xenopus egg extracts Chuanmao Zhang1,2, Mike Hughes1 and Paul R. Clarke1,* 1Biomedical Research Centre, University of Dundee, Level 5, Ninewells Hospital and Medical School, Dundee DD1 9SY, Scotland, UK 2Department of Cell Biology and Genetics, College of Life Sciences, Peking University, Beijing 100871, China *Author for correspondence (e-mail: [email protected]) Accepted 25 May; published on WWW 24 June 1999 SUMMARY Ran is an abundant GTPase of the Ras superfamily that is nucleus and blocks chromatin decondensation. In contrast, highly conserved in eukaryotes. In interphase cells, Ran is Ran GDP does not stabilise microtubules or inhibit nuclear mainly nuclear and thought to be predominantly GTP- assembly. RanT24N and RanBP1, which oppose the bound, but it is also present in the cytoplasm, probably generation of Ran-GTP by RCC1, arrest nuclear growth GDP-bound. This asymmetric distribution plays an after disappearance of the aster. Ran associates with important role in directing nucleocytoplasmic transport. microtubule asters in egg extracts and with mitotic spindles Ran has also been implicated in cell cycle control, including in somatic Xenopus cells, suggesting that it may affect the transition from mitosis to interphase when the microtubule stability directly. These results show that Ran compartmentalisation of the nucleus is established. Here, has a novel function in the control of microtubule stability we have examined the role of Ran in this transition using that is clearly distinct from nucleocytoplasmic transport.
    [Show full text]
  • Centrioles and the Formation of Rudimentary Cilia by Fibroblasts and Smooth Muscle Cells
    CENTRIOLES AND THE FORMATION OF RUDIMENTARY CILIA BY FIBROBLASTS AND SMOOTH MUSCLE CELLS SERGEI SOROKIN, M.D. From the Department of Anatomy, Harvard Medical School, Boston, Massachusetts ABSTRACT Cells from a variety of sources, principally differentiating fibroblasts and smooth muscle cells from neonatal chicken and mammalian tissues and from organ cultures of chicken duodenum, were used as materials for an electron microscopic study on the formation of rudimentary cilia. Among the differentiating tissues many cells possessed a short, solitary cilium, which projected from one of the cell's pair of centrioles. Many stages evidently intermediate in the fashioning of cilium from centriole were encountered and furnished the evidence from which a reconstruction of ciliogenesis was attempted. The whole process may be divided into three phases. At first a solitary vesicle appears at one end of a centriole. The ciliary bud grows out from the same end of the centriole and invaginates the sac, which then becomes the temporary ciliary sheath. During the second phase the bud lengthens into a shaft, while the sheath enlarges to contain it. Enlargement of the sheath is effected by the repeated appearance of secondary vesicles nearby and their fusion with the sheath. Shaft and sheath reach the surface of the cell, where the sheath fuses with the plasma membrane during the third phase. Up to this point, formation of cilia follows the classical descriptions in outline. Subsequently, internal development of the shaft makes the rudi- mentary cilia of the investigated material more like certain non-motile centriolar derivatives than motile cilia. The pertinent literature is examined, and the cilia are tentatively assigned a non-motile status and a sensory function.
    [Show full text]
  • Mitosin/CENP-F in Mitosis, Transcriptional Control, and Differentiation
    Journal of Biomedical Science (2006) 13: 205–213 205 DOI 10.1007/s11373-005-9057-3 Mitosin/CENP-F in mitosis, transcriptional control, and differentiation Li Ma1,2, Xiangshan Zhao1 & Xueliang Zhu1,* 1Laboratory of Molecular Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, 200031, China; 2Graduate School of Chinese Academy of Sciences, Beijing, 100039, China Ó 2006 National Science Council, Taipei Key words: differentiation, kinetochore, mitosis, transcription Summary Mitosin/CENP-F is a large nuclear/kinetochore protein containing multiple leucine zipper motifs poten- tially for protein interactions. Its expression levels and subcellular localization patterns are regulated in a cell cycle-dependent manner. Recently, accumulating lines of evidence have suggested it a multifunctional protein involved in mitotic control, microtubule dynamics, transcriptional regulation, and muscle cell differentiation. Consistently, it is shown to interact directly with a variety of proteins including CENP-E, NudE/Nudel, ATF4, and Rb. Here we review the current progress and discuss possible mechanisms through which mitosin may function. Mitosin, also named CENP-F, was initially iden- acid residues (GenBank Accession No. CAH73032) tified as a human autoimmune antigen [1, 2] and [3]. The gene expression is cell cycle-dependent, as an in vitro binding protein of the tumor suppressor the mRNA levels increase following S phase Rb [3, 4]. Its dynamic temporal expression and progression and peak in early M phase [3]. Such modification patterns as well as ever-changing patterns are regulated by the Forkhead transcrip- spatial distributions following the cell cycle pro- tion factor FoxM1 [5].
    [Show full text]