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Day 5
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Cell Division Cell Cycle & Mitosis
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Why Do Cells Divide? Cell growth Replace damaged or old cells
Larger cell is, the harder it is for cell to take in nutrients and eliminate waste. Replace damaged or old cells Form gametes (sex cells)
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Cell Division
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Cell Cycle Beginning of one cell until time that one cell divides into two cells Interphase – stage between divisions Mitosis is division of the nucleus Cytokinesis is division of cytoplasm and organelles Often the whole cell cycle is called mitosis, although this is not technically accurate
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Interphase
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Interphase Longest stage of Cell’s life Time spent between divisions
Produces all materials required for growth (metabolism) Preparation for division Chromosomes aren’t visible, in form of chromatin Centrioles(microtuble-organizing centers) replicate and one centriole moves to each pole. 3 phases: G1, S Phase, and G2
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G1 Phase of the Cell Cycle
Growth Phase Cell increases in size
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S Phase Synthesis Phase DNA duplicates Chromosomes duplicated
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Mitosis G2 checkpoint to make sure the DNA is correct
Cell prepares to divide Next step – Mitosis
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Interphase
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Terms to Know Chromosome - DNA coiled with proteins.
Chromatid - one side of the two strands a chromosome. Centromere - point at which the two chromatid attach. Spindle – cell structures made up of centrioles and microtubules fibers that move chromosomes during cell division. Homologous Chromosomes – pair of like chromosomes that code for same trait.
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Homologous Chromosomes
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Mitosis: Cell Division The last part of the Cell Cycle is Mitosis.
4 phases. Takes place in somatic cells (body cells)
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Phases of Mitosis
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Cytokinesis
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The Cell begins the division process
1.Prophase The Cell begins the division process Nucleolus disappears Nuclear membrane breaks apart
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Chromosomes become visible
Spindle apparatus forms from centrioles and attaches to centromeres.
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Prophase Chromosomes consisting of 2 Sister Chromatids
Pair of Centrioles Spindle Fibers
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The Second Phase of Mitosis
2. Metaphase The Second Phase of Mitosis Nuclear Membrane completely gone Duplicated chromosomes line up along the cell's equator.
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Metaphase Spindle Fibers Equator, or Metaphase Plate Chromosomes
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3. Anaphase The third phase of Mitosis
Diploid (pair) sets of daughter chromosomes separate They are pushed and pulled toward opposite poles of the cell by the spindle fibers
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Anaphase Daughter Chromosomes Chromatid Chromosome
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Spindle Fibers
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4. Telophase Separation of chromosomes completed
Cell Plate forms (plants) Cleavage furrow forms(animals) Nucleus & nucleolus reform Chromosomes uncoil
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Telophase Cleavage Furrow
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Cytokinesis – The final stage of Cell Cycle and Mitosis
The cytoplasm, organelles, and nuclear material are evenly split and two new cells are formed. Cell Plate
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Animals - cell pinches inward
Plants - a new cell wall forms between the two new cells
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Cancer
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What is Cancer? Cancer - disease where cells grow out of control and invade, erode and destroy normal tissue Cancer cells lack differentiation (not specialized) Normal cells enter the cell cycle only about 50 times; cancer cells can enter the cell cycle repeatedly. Normal cells undergo Apoptosis which is a programmed cell death to prevent overgrowth of cells.
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Cancer Development Abnormal cell growth called neoplasm
Abnormal growth results from the mutation of genes that regulate the cell cycle Carcinogenesis, the development of cancer is gradual—it may take decades before a cell has the characteristics of a cancer cell.
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Origin of Cancer Mutations in genes for repair enzymes of DNA can cause cancer. If proteins that start cell cycle or inhibit cell cycle are changed (mutated) it can cause cancer. Normal DNA segments have ends that shorten with each replication, eventually signaling the cell to end division; cancer cells have enzymes that keep their DNA segments at a constant length and thus the cells to continue dividing.
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Characteristics of Cancer Cells
Have abnormal nuclei Lack differentiation Chromosomes mutated; may be duplicated or deleted. Gene amplification, extra copies of genes Do not undergo apoptosis
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Characteristics cont. Do not have contact inhibition
Normal cells are anchored and stop dividing when in contact with other cells; Growth not inhibited and will invade and destroy normal tissue Cancer cells pile on top of each other to form a tumor. Cancer cells undergo metastasis and angiogenesis Metastasis – cancer spreads throughout body; new tumors away from primary tumor. Angiogenesis - formation of new blood vessels to bring nutrients and oxygen to tumor.
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Types of Tumors Benign: slow growth, non-invasive, no metastasis (not cancerous) Malignant: rapid growth, invasive, potential for metastasis (cancerous)
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Types of Cancers
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Is cancer a heritable disease?
There are heritable cancer syndromes but a majority are not. Cancer is a genetic disease, but the majority of mutations that lead to cancer are somatic (body cell)
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What causes the mutations that lead to cancer?
Viruses: HPV --> cervical cancer Bacteria: H. pylori --> gastric cancer Chemicals --> B[a]P --> lung cancer UV and ionizing radiation --> skin cancer What do these agents have in common? They are all Mutagens
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Treatments Surgery Chemotherapy Radiation Therapy Targeted Therapy
Immunotherapy Hyperhermia Bone Marrow and Peripheral Blood Stem Cell Transplant Laser Therapy Molecular Targeted Therapy
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7 ways to Reduce Risk Don’t use tobacoco
Eat healthy diet – fruits, veggies, limit alcohol Maintain healthy weight; physical activity Protect yourself from the sun Get immunized – Hepatitis B and HPV Avoid Risky behaviors – safe sex and no shared needles Take early detection seriously Self exams Regular doctor visits
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Meiosis Creating Cells for Sexual Reproduction
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Meiosis Takes place in Gametes(sex cells)
Produces a haploid cell (represented by N) People have 46 Chromosome or 23 pairs (2N) When an egg joins a sperm the count must stay at 46 to remain human egg can only have 23 sperm can only have 23 How does this happen?
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Definitions Diploid Cells- (2N)cells that have pairs of chromosomes. There are 2 of each chromosome in diploid cells. Haploid Cells- (N)cells that have only one of each chromosome. Haploid cells are used for sexual reproduction. Somatic Cells – body cells that are Diploid. Gametes or germ cells – sex cells that are Haploid.
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During Meiosis gamete (sex) cells undergo a “double division”, called Meiosis I and Meiosis II.
This maintains the DNA, but reducing the chromosomal count to 23. + = Sperm (23) Egg (23) = Fertilized Cell (46) Haploid Cells (N) Haploid Cells (N) Diploid Cells (2N)
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Meiosis I
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Prophase I Chromosomes already copied Centrioles separate
Nuclear membrane breaks down Crossing over occurs here
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Crossing Over Synapsis- Homologous Pairs line up = Tetrad
During synapsis the chromatids within a homologous pair may twist around each other and break off and attach to the other homologous pair = Crossing Over Results in exchange of genetic material between maternal and paternal chromosomes = genetic recombination
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Metaphase I Chromosome pairs line up at equator
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Anaphase I Chromosome pairs split Sister chromatids stay connected
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Telophase I Cell starts to divide in two
Nuclear membranes start to form again
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Meiosis II
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Prophase II Chromosomes do not replicate again
Cells have one set of sister chromatids Nuclear membrane breaks down Centrioles separate
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Metaphase II Sister chromatids line up at the middle of the cell
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Anaphase II Sister chromatids divide
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Telophase II Cells start to split in two
Each cell has one set of chromosomes—it is a haploid 4 cells form
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Original Gamete Metaphase Anaphase Telophase Cytokinesis
2 Daughter Cells Metaphase 2 Anaphase 2 Telophase 2 Cytokinesis – 4 Gametes
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OOGENESIS – Meiosis in females
SPERMATOGENESIS - Meiosis in Males
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Meiosis ensures that all living organisms maintain both Genetic Diversity and Genetic Integrity
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Cell Division in Prokaryotes
Lack a nucleus Have a single chromosome Reproduce by binary fission Include bacteria
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Steps in Binary Fission
Cells increase their cell mass slightly the single, circular bacterial chromosome is replicated Each cell divides into 2 daughter cells
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Mutations Ch. 10. pg
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Mutations Changes in nucleotide sequence of DNA
May occur in somatic cells (body cells) not passed to offspring May occur in gametes (eggs & sperm) passed to offspring
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Causes Mutations happen regularly
Any agent that causes a change in DNA is called a mutagen. Mutagens include radiation, chemicals, and even high temperatures. Ex. of radiation: X rays, cosmic rays, ultraviolet light, and nuclear radiation. Chemicals: Benzene Many mutations are repaired by enzymes.
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Are Mutations Helpful or Harmful?
Some harmful - Skin cancers and some leukemias result from somatic mutations Most mutations have no affect, some have detrimental affects and a few mutations may improve an organism’s survival (beneficial)
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Types of Mutations 2-Types
1. Gene mutations - change in one DNA sequence of a gene. 2.Chromosomal mutations – change in structure or loss or gain of part of a chromosome.
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Gene mutation- 2 types 1. Point Mutation
A change in a single base pair in DNA. Changes the amino acid in the protein Does not always cause a problem. THE DOG BIT THE CAT THE DOG BIT THE CAR
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2. Frameshift Mutation A single base is added or deleted from the DNA causing all the other bases to be out of position. More harmful than a regular point mutation. THE DOG BIT THE CAT THE DOB ITT HEC AT
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Chromosome Mutations Five types exist: Deletion Inversion
Translocation Nondisjunction Duplication
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Deletion Part of a chromosome is lost/deleted.
A B C D E F G H A B C E F G H
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Duplication/Insertion A part of the chromosome repeats
A B C D E F G H A B C B C D E F G H
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Inversion Part of a chromosome breaks off; reattaches backward
A B C D E F G H H A D C B E F G
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Translocation Part of a chromosome breaks off; attaches to a different chromosome that is not homologous A B C D E F G H W X A B C D E F G H W X Y Z Y Z W X Y Z Y Z Translocation Translocation
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Chromosome Mutation Animation
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Karyotyping Ch. 6 pg
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Some mutations that cause chromosomal abnormalities can be detected by analyzing a karyotype.
Karyotype – photo of the chromosomes in a dividing cell that shows the chromosomes arranged by size, number, and shape. Identifies gender and genetic disorders
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Amniocentesis – medical procedure used in prenatal diagnosis of chromosomal abnormalities and fetal infections small amount of amniotic fluid, which has fetal tissues, is extracted from the amniotic sac surrounding a developing fetus Autosomal abnormalities – abnormalities of chromosomes not directly involved in determining gender Sex Chromosomal abnormalities – abnormalities that affect the gender of an individual
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How Scientists Read Chromosomes?
To "read" a set of human chromosomes, scientists first use three key features to identify their similarities and differences: Size. This is the easiest way to tell two different chromosomes apart. Banding pattern. The size and location of Giemsa bands on chromosomes make each chromosome pair unique. Centromere position. Centromeres are regions in chromosomes that appear as a constriction. They have a special role in the separation of chromosomes into daughter cells during mitosis cell division (mitosis and meiosis). Image taken from: Using these key features, scientists match up the 23 pairs – one set from the mother and one set from the father.
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Typical Karyotype
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Typical Karyotype
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Trisomy 21- Down’s Syndrome - Karyotype
47 Total Chromosomes Three Chromosomes at the 21st Pair Image taken from:
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Monosomy X - Turner Syndrome - Karyotype
45 Total Chromosomes One “X” Chromosome Image taken from:
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XYY Karyotype 47 Total Chromosomes One “X” and Two “Y” Chromosomes
Image taken from:
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