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Mitosis/Meiosis Exam Review KEY Ramshaw – Biology Name ______________________ Hour ________ Date __________ Cell Cycle: 1. Complete the 4 missing labels for the cell cycle diagram. Shade in the parts that include interphase. G1 phase Cytokinesis! Mitosis S Phase G2 phase 2. What major events occur in each stage? (Include which stage most cells are in for about 90% of the time.) Interphase: G1 – organelles double, S – DNA doubles, G2 – DNA is checked for errors and cell grows. Cell spends about 90% of time in this phase. Mitosis – cell division CYTOKINESIS: cell splits into 2 new daughter cells 3. Does this cell cycle happen in prokaryotic or eukaryotic cells? Both 4. What happens if a cell enters the G0 phase? Give an example. It gets stuck in interphase and will never go through mitosis. Brain cells, heart cells, etc. Mitosis: 5. Define these vocabulary words: (you can find these in the glossary) Sister chromatid Centromere Spindle apparatus or spindle fibers Mitosis Chromatid Chromatin Cell plate Cleavage Furrow 6. Draw a picture of DNA as it is seen in each of the following stages: Chromatin (can’t draw this on the computer but it is loosely packed DNA, looks like a string that has been wadded up) Chromatid One straight line Chromosome (unreplicated) One straight line Sister Chromatids Looks like an X 7. Write a summary of what happens in each of these stages of mitosis. Include a simple picture. Prophase: nucleus disappears, chromosomes become visible, centrioles and spindle fibers spread apart Metaphase: Chromosomes line up down the equator Anaphase: sister chromatids pull apart Telophase: 2 new cells start to form (see your notes for pictures) 8. What is the result of mitosis? 2 new genetically identical cells. 9. Why do we need mitosis? To replace old or worn out cells, cells that have become sick, to grow (from childhood to adulthood) Cancer: 10. What is cancer? Uncontrolled mitosis (uncontrolled growth and division of cells) 11. What is the term used for substances that can cause cancer to happen? Carcinogens 12. What is cancer caused by? (2 answers) Unrepaired genetic changes or exposure to carcinogens 13. How is cancer often prevented? Explain. Cell cycle checkpoints, that monitor for DNA damage or spindle fiber failure and stop the cell cycle before cytokinesis 14. How does apoptosis help to prevent cancer? It kills cancerous cells before the divide and make more cancer cells 15. How does cancerous cell growth differ from normal cell growth? Cells that are growing normally respond to cell cycle control mechanisms. Cancer is uncontrolled mitosis that results when cells do not respond to cell cycle control mechanisms. Cancer cells can crowd out normal cells, causing loss of tissue function. Stem Cells: 16. Write a general description of each of the following: Embryonic Stem Cells – Cells taken from a blastocyst between days 6 and 12. They are not federally funded and there have been no cures from them yet. They are pluripotent (can become any type of cell). These are also very controversial because the inner cell mass that is taken out is what the baby would have been if it would have been implanted into a woman. Some people believe this is “killing a life”. Adult Stem Cells – Cells that have differentiated and are taken from a fully formed human and also from umbilical cords. These are federally funded and have cured people of diseases. iPs Cells – the newest kind of stem cell. They are pluripotent adult stem cells. They work backwards and turn adult somatic cells into “embryonic like” cells and then can be turned into the type of cell the patient needs. These are federally funded. 17. How would Somatic Cell Nuclear Transfer help someone cure themselves of a spinal cord injury? They would grow their own identical twin to the blastocyst stage, harvest the inner cell mass, create spinal cord cells from those embryonic stem cells and cure themselves. 18. Define the following terms: (you can find these on the back of you stem cell web that we did in class) Teratoma Pluripotent Blastocyst Inner cell mass Cloning Differentiated Undifferentiated 19. Briefly discuss the ethical arguments against some of these types of stem cells. Identify which ones are involved in the ethical arguments and are not federally funded. (see my answer for number 16) Meiosis: 20. Define these terms: (you can find these in the glossary) Homologous Chromosomes (or homologues) Synapsis Tetrad Crossing Over Independent Assortment Diploid Haploid Gametes Oogenesis Polar bodies Spermatogenesis Somatic cell 21. Meiosis is a special kind of cell division. It consists of _1__ replication of the DNA followed by __2__ cell divisions. 22. Why does meiosis reduce the chromosome number in gametes? So the egg has half the chromosomes and the sperm has half, when they come together the zygote has the correct number of chromosomes (is diploid). 23. Are any of the final cells created in meiosis the same? Why or why not? No, the chromosomes have gone through crossing over and independent assortment. 24. Using the knowledge you have gained about meiosis to explain why people look different from their brothers and sisters. Each egg and each sperm are unique. When each life is created, it is a different combination of DNA from your mom and dad. 25. Draw out the process of meiosis, starting with Prophase I and ending with Telophase II. Use your Trogdor Meiosis to do this one! 26. Compare and contrast mitosis and meiosis: Answer each of the following 5 questions for mitosis & meiosis. 1. 2. 3. 4. 5. The type of cell (somatic or gamete) that undergoes this process If the daughter cells are genetically identical the parent or not If the resulting daughter cells are diploid or haploid The purpose of the process (replace old/sick cells or to make reproductive cells) The names of all the stages they go through in the process Mitosis 1. 2. 3. 4. 5. somatic cells genetically identical diploid replace old/sick cells interphase, prophase, metaphase, anaphase, telophase, cytokinesis! Meiosis 1. 2. 3. 4. 5. gametes not genetically identical haploid make reproductive cells interphase, prophase I, metaphaseI, anaphaseI, telophaseI, prophaseII, metaphaseII, anaphaseII, telophaseII AND CYTOKINESIS!