Lecture 2, Ch 12, Cell Cycle

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    Copyright 2005 Pearson Education, Inc. publishing as Benjamin Cummings

    PowerPoint Lectures forBiology, Seventh Edition

    Neil Campbell and Jane Reece

    Lectures by Chris Romero

    Chapter 12

    The Cell Cycle

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    Copyright 2005 Pearson Education, Inc. publishing as Benjamin Cummings

    Overview: The Key Roles of Cell Division

    The ability of organisms to reproduce bestdistinguishes living things from non-living matter

    The continuity of life is based upon thereproduction of cells, or cell division

    Cell division is integral part of cell cycle

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    Types of cell division

    Prokaryotes

    Binary fission

    Eukaryotes

    Mitosis:

    Growth, development & repair

    Asexual reproduction (yields genetically identical cells)

    Occurs in somatic (body) cells

    Meiosis:

    Sexual reproduction (yields genetically different cells with halfthe # of chromosomes)

    Occurs in specific reproductive cells

    Yields gametes (e.g., eggs & sperm) or spores

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    Eukaryotic cell division consists of:

    Mitosis, the division of the nucleus

    Cytokinesis, the division of the cytoplasm

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    Concept 12.1: Mitotic cell division results ingenetically identical daughter cells

    Cells duplicate their genetic material before theydivide, ensuring that each daughter cell receivesan exact copy of the genetic material, DNA

    A dividing cell duplicates its DNA, allocates thetwo copies to opposite ends of the cell, and onlythen splits into daughter cells

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    Cellular Organization of the Genetic Material

    A cells endowment of DNA (its genetic

    information) is called its genome

    DNA molecules* in a cell are packaged intochromosomes

    *Prokaryotes-circular DNA

    Eukaryotes-linear DNA

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    Every eukaryotic species has a characteristicnumber of chromosomes in each cell nucleus

    Somatic (non-reproductive) cells (normally) havetwo sets of chromosomes

    Gametes (reproductive cells: sperm and eggs)(and spores) have half as many chromosomes assomatic cells

    Eukaryotic chromosomes consist of chromatin, acomplex of DNA and protein that condensesduring cell division

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    DNA associates with special proteins to form more stable

    structure called chromosomes (different proteins inprokaryotes and eukaryotes, so chromosomes built different)

    Chromosomes are found inside nucleus in eukaryotes

    Human - 46 chromosomes, 23 pairs (1 set of 23 from egg, 1set of 23 from sperm)

    Each chromosome contains many genes

    Gene is a segment of DNA that is responsible for controllinga trait (e.g., coding for a specific protein)

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    Human female karyotype

    H l k

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    Human male karyotype

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    Phases 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)

    Interphase (about 90% of the cell cycle) can bedivided into subphases:

    G1phase (first gap) S phase (synthesis)

    G2phase (second gap)

    LE 12 5

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    LE 12-5

    G1

    G2

    S(DNA synthesis)

    INTERPHASE

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    Distribution of Chromosomes During Cell Division

    In preparation for cell division, DNA is replicated

    and the chromosomes condense

    Each duplicated chromosome has two sisterchromatids, which separate during cell division

    The centromere is the narrow waist of the

    duplicated chromosome, where the twochromatids are most closely attached

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    LE 12-4

    Chromosomeduplication(including DNAsynthesis)

    0.5 m

    Centromere

    Sisterchromatids

    Separation

    of sisterchromatids

    Centromeres Sister chromatids

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    Mitosis is conventionally divided into five phases:

    Prophase

    Prometaphase

    Metaphase

    Anaphase

    Telophase

    Cytokinesis is well underway by late telophase

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    1. Prophase

    - Chromatin condenses, this causes the chromosomes tobegin to become visible

    - Centrosomes separate, moving to opposite ends of thenucleus

    - The centrosomes start to form a framework used toseparate the two sister chromatids called the mitoticspindle, that is made of microtubules

    - Nucleolus disappears

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    2. Prometaphase

    - Nuclear envelope fragments

    - Chromosomes become more condensed

    - A kinetochore is formed at the centromere, the point wherethe sister chromatids are attached

    - Microtubules attach at the kinetochores

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    3. Metaphase

    - Chromosomes align on an axis called the metaphase plate

    - Note: the spindle consists of microtubules, one attached toeach chromosome

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    4. Anaphase

    - Each centromere splits making two chromatids free

    - Each chromatid moves toward a pole

    - Cell begins to elongate, caused by microtubules notassociated with the kinetochore

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    5. Telophase

    Formation of nuclear membrane and nucleolus

    Short and thick chromosomes begin to elongate to formlong and thin chromatin

    Formation of the cleavage furrow - a shallow groove inthe cell near the old metaphase plate

    Cytokinesis = division of the cytoplasm

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    Mitosis in an onion root

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    Th Mit ti S i dl A Cl L k

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    The Mitotic Spindle:A Closer Look

    The mitotic spindle is an apparatus of

    microtubules that controls chromosome movementduring mitosis

    Assembly of spindle microtubules begins in the

    centrosome, the microtubule organizing center

    The centrosome replicates, forming twocentrosomes that migrate to opposite ends of the

    cell, as spindle microtubules grow out from them

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

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    The spindle includes the centrosomes, the spindle

    microtubules, and the asters

    Some spindle microtubules attach to thekinetochores of chromosomes and move the

    chromosomes to the metaphase plate

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    Microtubules ChromosomesSisterchromatids

    AsterCentrosome

    Metaphaseplate

    Kineto-chores

    Kinetochoremicrotubules

    0.5 m

    Overlapping

    nonkinetochoremicrotubules

    1 mCentrosome

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    In anaphase, sister chromatids separate and

    move along the kinetochore microtubules towardopposite ends of the cell

    The microtubules shorten by depolymerizing at

    their kinetochore ends

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    Chromosomemovement

    Microtubule Motorprotein

    Chromosome

    Kinetochore

    Tubulinsubunits

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    Nonkinetochore microtubules from opposite polesoverlap and push against each other, elongatingthe cell

    In telophase, genetically identical daughter nuclei

    form at opposite ends of the cell

    Cytokinesis: A Closer Look

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    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

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    Cleavage furrow

    100 m

    Contractile ring ofmicrofilaments

    Daughter cells

    Cleavage of an animal cell (SEM)

    Mitosis

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    LE 12-9b

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    1 m

    Daughter cells

    Cell plate formation in a plant cell (TEM)

    New cell wallCell plate

    Wall ofparent cell

    Vesiclesformingcell plate

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    Nucleus

    Cell plateChromosomesNucleolus

    Chromatin

    condensing 10 m

    Prophase. Thechromatin is condensing.The nucleolus isbeginning to disappear.Although not yet visiblein the micrograph, the

    mitotic spindle is startingto form.

    Prometaphase. Wenow see discretechromosomes; eachconsists of two identicalsister chromatids. Laterin prometaphase, the

    nuclear envelope willfragment.

    Metaphase. The spindle iscomplete, and thechromosomes, attachedto microtubules at theirkinetochores, are all atthe metaphase plate.

    Anaphase. Thechromatids of eachchromosome haveseparated, and thedaughter chromosomesare moving to the ends of

    the cell as theirkinetochore micro-tubules shorten.

    Telophase. Daughternuclei are forming.Meanwhile, cytokinesishas started: The cellplate, which will dividethe cytoplasm in two, is

    growing toward theperimeter of the parentcell.

    Binary Fission

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    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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    Origin ofreplication

    Cell wall

    Plasmamembrane

    Bacterial

    chromosome

    E. colicell

    Two copiesof origin

    Chromosomereplication begins.Soon thereafter,one copy of the originmoves rapidly toward

    the other end of the cell.

    LE12-11_2

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    Origin ofreplication

    Cell wall

    Plasma

    membraneBacterialchromosome

    E. colicell

    Two copiesof origin

    Chromosomereplication begins.Soon thereafter,

    one copy of the originmoves rapidly towardthe other end of the cell.

    Replication continues.One copy of the originis now at each end ofthe cell.

    Origin Origin

    LE 12-11_3

    O i i fCell wall

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    Origin ofreplication

    Cell wall

    Plasmamembrane

    Bacterialchromosome

    E. colicell

    Two copies

    of origin

    Chromosome

    replication begins.Soon thereafter,one copy of the originmoves rapidly towardthe other end of the cell.

    Replication continues.

    One copy of the originis now at each end ofthe cell.

    Origin Origin

    Replication finishes.The plasma membrane

    grows inward, andnew cell wall isdeposited.

    Two daughtercells result.

    The Evolution of Mitosis

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    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 andmitosis

    LE 12-12Bacterial

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    chromosome

    Chromosomes

    Microtubules

    Prokaryotes

    Dinoflagellates

    Intact nuclearenvelope

    Kinetochoremicrotubules

    Kinetochoremicrotubules

    Intact nuclearenvelope

    Diatoms

    Centrosome

    Most eukaryotes

    Fragments ofnuclear envelope

    Concept 12.3: The cell cycle is regulated by a

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    Concept 12.3: The cell cycle is regulated by amolecular control system

    The frequency of cell division varies with the typeof cell and with cell happiness

    These cell cycle differences result from regulationat the molecular level

    The cell cycle appears to be driven by specificchemical signals present in the cytoplasm

    The levels of these chemical signals are

    influenced by biotic & abiotic factors

    The Cell Cycle Control System

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    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 clock has specific checkpoints where the cell

    cycle stops until a go-ahead signal is received

    For many cells, the G1 checkpoint seems to be themost important one

    LE 12-14G1 checkpoint

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    G1 checkpoint

    G1S

    M

    M checkpoint

    G2 checkpoint

    G2

    Controlsystem

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    G1

    G1 checkpoint

    G1

    G0

    If a cell receives a go-aheadsignal at the G1 checkpoint,the cell continues on in thecell cycle.

    If a cell does not receive ago-ahead signal at the G1checkpoint, the cell exits thecell cycle and goes into G0, anondividing state.

    LE12-16b

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    Degradedcyclin G2

    checkpoint

    Cdk

    Cyclin isdegraded

    MPFCyclin

    Cdk

    Molecular mechanisms that help regulate the cell cycle

    Stop and Go Signs: Internal and External Signals at

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    p g gthe Checkpoints An example of an internal signal is that

    kinetochores not attached to spindlemicrotubules send a molecular signal thatdelays anaphase

    Some external signals are growth factors,proteins released by certain cells that stimulateother cells to divide

    For example, platelet-derived growth factor(PDGF) stimulates the division of humanfibroblast cells in culture

    LE 12-17Scalpels

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    Petriplate

    p

    Without PDGF

    With PDGF

    Without PDGF

    With PDGF

    10 mm

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    Another example of external signals is density-

    dependent inhibition, in which crowded cells stopdividing

    Most animal cells also exhibit anchorage

    dependence, in which they must be attached to asubstratum in order to divide

    LE 12-18aCells anchor to dish surface and

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    divide (anchorage dependence).

    When cells have formed a completesingle layer, they stop dividing(density-dependent inhibition).

    If some cells are scraped away, theremaining cells divide to fill the gap andthen stop (density-dependent inhibition).

    25 mNormal mammalian cells

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    Cancer cells exhibit neither density-dependentinhibition nor anchorage dependence

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    Cancer cells do not exhibit

    anchorage dependenceor density-dependent inhibition.

    Cancer cells25 m

    Loss of Cell Cycle Controls in Cancer Cells

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    y

    Cancer cells do not respond normally to the

    bodys control mechanisms

    Cancer cells form tumors, masses of abnormalcells within otherwise normal tissue

    If abnormal cells remain at the original site, thelump is called a benign tumor

    Malignant tumors invade surrounding tissues andcan metastasize, exporting cancer cells to otherparts of the body, where they may form secondarytumors