| Chapter 17 From Gene to Protein | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Chapter 17 From Gene to Protein | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| CHAPTER 1 INTRODUCTION: THEMES IN THE STUDY OF LIFE | |
| OBJECTIVES | |
| Exploring Life on Its Many Levels
1. Briefly describe the unifying themes that characterize the biological sciences. 2. Diagram the hierarchy of structural levels in biological organization. 3. Explain how the properties of life emerge from complex organization. 4. Describe the two major dynamic processes of any ecosystem. 5. Distinguish between prokaryotic and eukaryotic cells. 6. Describe the basic structure and function of DNA. 7. Describe the dilemma of reductionism. 8. Discuss the goals and activities of systems biology. List three research developments that have advanced systems biology. 9. Explain the importance of regulatory mechanisms in living things. Distinguish between positive and negative feedback. Evolution, Unity, and Diversity 10. Distinguish among the three domains of life. List and distinguish among the three kingdoms of multicellular, eukaryotic life. 11. Explain the phrase “life’s dual nature of unity and diversity.” 12. Describe the observations and inferences that led Charles Darwin to his theory of evolution by natural selection. 13. Explain why diagrams of evolutionary relationships have a treelike form. The Process of Science 14. Distinguish between discovery science and hypothesis-based science. Explain why both types of exploration contribute to our understanding of nature. 15. Distinguish between quantitative and qualitative data. 16. Distinguish between inductive and deductive reasoning. 17. Explain why hypotheses must be testable and falsifiable but are not provable. 18. Describe what is meant by a controlled experiment. 19. Distinguish between the everyday meaning of the term theory and its meaning to scientists. 20. Explain how science is influenced by social and cultural factors. 21. Distinguish between science and technology. Explain how science and technology are interdependent.
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| Chapter 18 Genetics of Viruses & Bacteria | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Chapter 26 Early Earth & the Origin of Life | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Chapter 19 Eukaryotic Genomes | ||
| Objectives | ||
| The Structure of Eukaryotic Chromatin
1. Compare the structure and organization of prokaryotic and eukaryotic genomes. 2. Describe the current model for progressive levels of DNA packing in eukaryotes. 3. Explain how histones influence folding in eukaryotic DNA. 4. Distinguish between heterochromatin and euchromatin. The Control of Gene Expression 5. Explain the relationship between differentiation and differential gene expression. 6. Describe at what level gene expression is generally controlled. 7. Explain how DNA methylation and histone acetylation affect chromatin structure and the regulation of transcription. 8. Define epigenetic inheritance. 9. Describe the processing of pre-mRNA in eukaryotes. 10. Define control elements and explain how they influence transcription. 11. Distinguish between general and specific transcription factors. 12. Explain the role that promoters, enhancers, activators, and repressors may play in transcriptional control. 13. Explain how eukaryotic genes can be coordinately expressed and give some examples of coordinate gene expression in eukaryotes. 14. Describe the process and significance of alternative RNA splicing. 15. Describe factors that influence the life span of mRNA in the cytoplasm. Compare the longevity of mRNA in prokaryotes and in eukaryotes. 16. Explain how gene expression may be controlled at the translational and post-translational level. The Molecular Biology of Cancer 17. Distinguish between proto-oncogenes and oncogenes. Describe three genetic changes that can convert proto-oncogenes into oncogenes. 18. Explain how mutations in tumor-suppressor genes can contribute to cancer. 19. Explain how excessive cell division can result from mutations in the ras proto-oncogenes. 20. Explain why a mutation knocking out the p53 gene can lead to excessive cell growth and cancer. Describe three ways that p53 prevents a cell from passing on mutations caused by DNA damage. 21. Describe the set of genetic factors typically associated with the development of cancer. 22. Explain how viruses can cause cancer. Describe several examples. 23. Explain how inherited cancer alleles can lead to a predisposition to certain cancers. Genome Organization at the DNA Level 24. Describe the structure and functions of the portions of eukaryotic DNA that do not encode protein or RNA. 25. Distinguish between transposons and retrotransposons. 26. Describe the structure and location of Alu elements in primate genomes. 27. Describe the structure and possible function of simple sequence DNA. 28. Using the genes for rRNA as an example, explain how multigene families of identical genes can be advantageous for a cell. 29. Using a-globin and b-globin genes as examples, describe how multigene families of nonidentical genes may have evolved. 30. Define pseudogenes. Explain how such genes may have evolved. 31. Describe the hypothesis for the evolution of a-lactalbumin from an ancestral lysozyme gene. 32. Explain how exon shuffling could lead to the formation of new proteins with novel functions. 33. Describe how transposition of an Alu element may allow the formation of new genetic combinations while retaining gene function.
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