Dispatch 1) Explain the structure and function of a chromosome 2) Copy and fill in Organism Diploid # (in somatic cells) Haploid # (in gametes) Cat Rose.

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Presentation transcript:

Dispatch 1) Explain the structure and function of a chromosome 2) Copy and fill in Organism Diploid # (in somatic cells) Haploid # (in gametes) Cat Rose Goat Rice Dog Chimpanzees

Chapter 12 The Cell Cycle

http://highered. mcgraw-hill http://highered.mcgraw-hill.com/sites/0072495855/student_view0/chapter2/animation__how_the_cell_cycle_works.html

Mitosis in Action Spindle=_________ Nucleus=_________ Cell Membrane=______ Chromosome=______

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

Concept 12.1: Cell division results in genetically identical daughter cells Cells duplicate their genetic material before they divide, ensuring that each daughter cell receives an exact copy of the genetic material, DNA A dividing cell duplicates its DNA, allocates the two copies to opposite ends of the cell, and only then splits into daughter cells

Cellular Organization of the Genetic Material A cell’s endowment of DNA (its genetic information) is called its genome DNA molecules in a cell are packaged into chromosomes

Every eukaryotic species has a characteristic number of chromosomes in each cell nucleus Somatic (nonreproductive) 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, a complex of DNA and protein that condenses during cell division

Distribution of Chromosomes During 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

LE 12-4 0.5 µm Chromosome duplication (including DNA synthesis) Centromere Sister chromatids Separation of sister chromatids Centromeres Sister chromatids

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

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 be divided into subphases: G1 phase (“first gap”) S phase (“synthesis”) G2 phase (“second gap”)

INTERPHASE S (DNA synthesis) LE 12-5 INTERPHASE S (DNA synthesis) G1 Cytokinesis Mitosis G2 MITOTIC (M) PHASE

http://bio.rutgers.edu/~gb101/lab2_mitosis/section2_frames.html

The Mitotic Spindle: A Closer Look The mitotic spindle is an apparatus of microtubules that controls chromosome movement during mitosis 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 An aster (a radial array of short microtubules) extends from each centrosome

LE 12-7 Aster Centrosome Sister chromatids Microtubules Chromosomes Metaphase plate Kineto- chores Overlapping nonkinetochore microtubules Kinetochore microtubules Centrosome 1 µm 0.5 µm

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

Chromosome movement Kinetochore Tubulin subunits Motor Microtubule LE 12-8b Chromosome movement Kinetochore Tubulin subunits Motor protein Microtubule Chromosome

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

LE 12-9a 100 µm Cleavage furrow Contractile ring of microfilaments Daughter cells Cleavage of an animal cell (SEM)

LE 12-9b Vesicles forming cell plate Wall of parent cell 1 µm Cell plate New cell wall Daughter cells Cell plate formation in a plant cell (TEM)

LE 12-10 Chromatin condensing Nucleus Chromosomes Cell plate 10 µm Nucleolus Prophase. The chromatin is condensing. The nucleolus is beginning to disappear. Although not yet visible in the micrograph, the mitotic spindle is starting to form. Prometaphase. We now see discrete chromosomes; each consists of two identical sister chromatids. Later in prometaphase, the nuclear envelope will fragment. Metaphase. The spindle is complete, and the chromosomes, attached to microtubules at their kinetochores, are all at the metaphase plate. Anaphase. The chromatids of each chromosome have separated, and the daughter chromosomes are moving to the ends of the cell as their kinetochore micro- tubules shorten. Telophase. Daughter nuclei are forming. Meanwhile, cytokinesis has started: The cell plate, which will divide the cytoplasm in two, is growing toward the perimeter of the parent cell.

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

Chromosome replication begins. Soon thereafter, LE 12-11_1 Cell wall Origin of replication Plasma membrane E. coli cell Bacterial chromosome Chromosome replication begins. Soon thereafter, one copy of the origin moves rapidly toward the other end of the cell. Two copies of origin

Chromosome replication begins. Soon thereafter, LE 12-11_2 Cell wall Origin of replication Plasma membrane E. coli cell Bacterial chromosome Chromosome replication begins. Soon thereafter, one copy of the origin moves rapidly toward the other end of the cell. Two copies of origin Origin Origin Replication continues. One copy of the origin is now at each end of the cell.

LE 12-11_3 Cell wall Origin of replication Plasma membrane E. coli cell Bacterial chromosome Chromosome replication begins. Soon thereafter, one copy of the origin moves rapidly toward the other end of the cell. Two copies of origin Origin Origin Replication continues. One copy of the origin is now at each end of the cell. Replication finishes. The plasma membrane grows inward, and new cell wall is deposited. Two daughter cells result.

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

This man has cancer of the mouth.

http://science. education. nih http://science.education.nih.gov/supplements/nih1/cancer/activities/activity2_animations.htm

What is Cancer? Cancer means uncontrolled cell growth The body needs to keep cell growth = cell death Cell cycle checkpoints kill mutated or old cells

Cell Cycle Checkpoints Mutated cancer cells skip cell cycle checkpoints at the end of: G1: Is the cell big enough? G2: Is the cell ready for mitosis? Mitosis: Does the body need more cells?

G1 Phase S Phase Mitosis Cytokinesis G2 Phase The cell cycle has traffic lights that serve as checkpoints Is the cell big enough? G1 Phase S Phase Mitosis Cytokinesis G2 Phase Does the body need more cells? Is the cell ready for mitosis?

Cancer is caused when the checkpoints are broken and the cell cycle keeps going without stopping G1 Phase S Phase Mitosis Cytokinesis G2 Phase

What are the types of cancer? *Any part of the body can be cancerous Skin cancer Lung cancer Breast cancer Testicular cancer Colon cancer Liver cancer Brain cancer Lung Cancer Brain Cancer

How do you get cancer? How can you get cancer? Getting hit in the breast? NO Having unprotected sex? Smoking? YES Being in the sun too long?

Why is cancer so deadly? * 1) Mutated cells beat the cell cycle checkpoints and keep dividing 2) They form tumors which then stop your body parts from functioning normally 3) Angiogensis – the tumors hijack blood vessels to keep them alive 4) Metastisis – the cells from the tumor travel and infect other parts of your body *

Cancer Animation http://www.pbs.org/wgbh/nova/cancer/grow_flash.html

Here is the development of colon cancer.

Why is Cancer so Hard to Cure? It is a silent killer, by the time it is found it is already to late 2) Chemo/Radiation therapy can kill cancer cells, but is hard on patients 3) If one cancer cell survives, or travels, cancer will come back

Can cancer be prevented? Cancer is not contagious. There is no guaranteed way to prevent cancer, people can reduce their risk (chance) of developing cancer by: A) not using tobacco products B) choosing foods with less fat and eating more vegetables, fruits, and whole grains C) exercising regularly and maintaining a lean weight D) avoiding the harmful rays of the sun, using sunblock, and wearing clothing that protects the skin

G1 checkpoint Control system S G1 G2 M M checkpoint G2 checkpoint LE 12-14 G1 checkpoint Control system S G1 G2 M M checkpoint G2 checkpoint

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

LE 12-15 G0 G1 checkpoint G1 G1 If a cell receives a go-ahead signal at the G1 checkpoint, the cell continues on in the cell cycle. If a cell does not receive a go-ahead signal at the G1 checkpoint, the cell exits the cell cycle and goes into G0, a nondividing state.

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

Relative concentration LE 12-16a M G1 S G2 M G1 S G2 M MPF activity Cyclin Relative concentration Time Fluctuation of MPF activity and cyclin concentration during the cell cycle

Molecular mechanisms that help regulate the cell cycle LE 12-16b G1 Cyclin S Cdk Degraded cyclin M G2 accumulation G2 checkpoint Cdk Cyclin is degraded Cyclin MPF Molecular mechanisms that help regulate the cell cycle

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

LE 12-17 Scalpels Petri plate Without PDGF With PDGF Without PDGF 10 mm

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

Cells anchor to dish surface and divide (anchorage dependence). LE 12-18a 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 Normal mammalian cells

Cancer cells exhibit neither density-dependent inhibition nor anchorage dependence

Cancer cells do not exhibit anchorage dependence LE 12-18b Cancer cells do not exhibit anchorage dependence or density-dependent inhibition. 25 µm Cancer cells

Loss of Cell Cycle Controls in Cancer Cells Cancer cells do not respond normally to the body’s control mechanisms 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

LE 12-19 Lymph vessel Tumor Blood vessel Glandular tissue Metastatic Cancer cell A tumor grows from a single cancer cell. Cancer cells invade neighboring tissue. Cancer cells spread through lymph and blood vessels to other parts of the body. A small percentage of cancer cells may survive and establish a new tumor in another part of the body.

Mitosis vs. Meiosis