AP Biology 2010 Week 5 Part I-Cell Communication and Cell Cycle: Focus on Mitosis/ Meiosis Chapter 11: Cell Communication Chapter 12: The Cell Cycle College Board Performance Objectives: Explain how the cell cycle assures genetic continuity. Explain how mitosis allows for the even distribution of genetic information to new cells. What are the mechanisms of cytokinesis? Describe how the cell cycle is regulated. Explain how aberrations in the cell cycle can lead to tumor formation. Describe and explain the events of mitosis in animal and plant cells. College Board Lab Objectives: Pacing Guide: Chapter 11: Cell Communication—1.5 days Chapter 12: The Cell Cycle—1.5 days Key Words: signal-transduction pathway local regulator hormone G-protein- receptor tryosine kinase protein kinase receptor protein phosphatases second messengers cyclic AMP, diacylglycerol inositol trisphosphate calmodulin genome somatic cells gametes chromatin sister chromatids centromere mitosis cytokinesis meiosis mitotic (M) phase interphase Ross 2010 SJDA G1 phase S phase G2 phase prophase metaphase anaphase telophase mitotic spindle kinetochore metaphase plate cleavage furrow cell plate binary fission cell-cycle control system checkpoint G0 phase growth factor density-dependent inhibition tumor benign malignant metastasis Page 1 AP Biology 2010 Chapter 11 Assignment # 5 Cell Communication 1. Describe the basic signal-transduction pathway used for mating in yeast. Explain why we believe these pathways evolved before the first multicellular organisms appeared on Earth. 2. Define paracrine signaling and give an example. 3. Define local regulation and explain why hormones are not local regulators. 4. Explain how plant and animal hormones travel to target cells. 5. List and briefly define the three stages of cell signaling. 6. Describe the nature of a ligand-receptor interaction and state how such interactions initiate a signal-transduction system. 7. State where signal receptors may be located in target cells. 8. Compare and contrast G-protein-linked receptors, tyrosine-kinase receptors, and ligandgated ion channels. 9. Describe two advantages of using a multistep pathway in the transduction stage of cell signaling. 10. Explain how the original signal molecule can produce a cellular response when it may not even enter the target cell. 11. Describe how phosphorylation propagates signal information. 12. Explain why a single cell may require hundreds of different protein kinases. 13. Explain how protein phosphatases turn off signal-transduction pathways. 14. Define the term second messenger. Briefly describe the role of these molecules in signaling pathways. 15. Describe how cyclic AMP is formed and how it propagates signal information in target cells. 16. Explain how the cholera bacterium causes the symptoms of cholera by disrupting Gprotein-signaling pathways. 17. Describe how the cytosolic concentration of Ca2+ can be altered and how the increased pool of Ca2+ is involved with signal transduction. 18. Describe how signal information is transduced into cellular responses in the cytoplasm and in the nucleus. 19. Describe how signal amplification is accomplished in target cells. 20. Explain why different types of cells may respond differently to the same signal molecule. 21. Explain how scaffolding proteins help to coordinate a cell’s response to incoming signals. Ross 2010 SJDA Page 2 AP Biology 2010 Chapter 12:The cell cycle 1. Explain how cell division functions in reproduction, growth, and repair. 2. Describe the structural organization of a prokaryotic and a eukaryotic genome. 3. Describe the major events of cell division that enable the genome of one cell to be passed on to two daughter cells. 4. Describe how chromosome number changes throughout the human life cycle. 5. List the phases of the cell cycle and describe the sequence of events that occurs during each phase. 6. List the phases of mitosis and describe the events characteristic of each phase. 7. Recognize the phases of mitosis from diagrams and micrographs. 8. Draw or describe the spindle apparatus, including centrosomes, kinetochore microtubules, non kinetochore microtubules, asters, and centrioles (in animal cells). 9. Describe what characteristic changes occur in the spindle apparatus during each phase of mitosis. 10. Explain the current models for “pole ward” chromosomal movement and elongation of the cell’s polar axis. 11. Compare cytokinesis in animals and in plants. 12. Describe the process of binary fission in bacteria and explain how eukaryotic mitosis may have evolved from binary fission. 13. Describe the roles of checkpoints, cyclin, Cdk, and MPF in the cell cycle control system. 14. Describe the internal and external factors that influence the cell cycle control system. 15. Explain how the abnormal cell division of cancerous cells escapes normal cell cycle controls. 16. Distinguish among benign, malignant, and metastatic tumors. Ross 2010 SJDA Page 3 AP Biology 2010 Part II Genetics Chapter 13: Meiosis and Sexual Life Cycles Chapter 14: Mendel and the Gene Idea College Board Performance Objectives: Describe features of meiosis that are important in sexual reproduction. Explain why meiosis is important in heredity. Explain how meiosis is related to gametogenesis. Explain the key mechanical and genetic differences between meiosis and mitosis. Explain how Mendel's work laid the foundation of modern genetics. Explain the principal patterns of inheritance. College Board Lab Objectives: Recognize the stages of mitosis in a plant or animal cell. Calculate the relative duration of the cell cycle stages. Describe how independent assortment and crossing-over can generate genetic variation among the products of meiosis. Use chromosome models to demonstrate the activity of chromosomes during Meiosis I and Meiosis II. Relate chromosome activity to Mendelian segregation and independent assortment. Calculate the map distance of a particular gene from a chromosome's center for between two genes using an organism of your choice in a controlled experiment. Demonstrate the role of meiosis in the formation of gametes using an organism of your choice, in a controlled experiment. Compare and contrast the results of meiosis and mitosis in plant cells. Compare and contrast the results of meiosis and mitosis in animal cells. Suggested Laboratory Experiments: Biology AP* Laboratory 3, Mitosis and Meiosis and Lab Topic 7 Pacing Guide: Chapter 13: Meiosis and Sexual Life Cycles-2.0 days Chapter 14: Mendel and the Gene Idea-2.0 days Ross 2010 SJDA Page 4 AP Biology 2010 Assignment continued Chapter 13: Meiosis and Sexual Life Cycles 1. Describe the organization of the chromosome. Include the terms centromere, chromatin, sister chromatids. 2. List the phases of the cell cycle, and briefly describe the events in each stage. 3. What is the purpose of mitosis? 4. List the stages of mitosis and summarize the events in each phase. 5. Describe the structure and function of the mitotic spindle. 6. If there are 20 centromeres in a cell, how many chromosomes are there? 7. Explain the process of cytokinesis in animals. How does this process differ in plant cells? 8. Discuss the factors that control cell division. Include growth factors, density-dependent inhibition, restriction point, and regulatory proteins. 9. Describe the nature of cancer cells. Chapter 14: Mendel and the Gene Idea 1. Describe the four ideas which have come from Mendel's hypothesis concerning inheritance. 2. Define homozygous, heterozygous, phenotype, and genotype. 3. What is a testcross and how is it useful? 4. Understand how to construct a Punnett square and use it to predict genotypic and phenotypic ratios. 5. Define the rule of multiplication and the rule of addition. 6. Define complete dominance, incomplete dominance, codominance, multiple alleles, pleiotropy, epistasis, and polygenic inheritance. 7. Explain how one allele can be dominant over another at the molecular level. 8. How is a pedigree used in genetics? 9. Distinguish between recessively and dominantly inherited disorders? What is meant by the term linked genes? 10. Looking at progeny, how might one guess that two genes are linked? 11. When studying linked genes, how do you explain the appearance of progeny that do not share either parental phenotype? 12. How can recombination data be used to map genetic loci? 13. How does a linkage map differ from an actual picture of a chromosome? 14. Describe the X-Y, X-O, Z-W, and haploid-diploid systems of sex determination. Ross 2010 SJDA Page 5