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| Chapter 17 From Gene to Protein | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Chapter 18 Genetics of Viruses & Bacteria | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Chapter 19 Eukaryotic Genomes | ||
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| 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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Chapter 1 Exploring Life Lecture Outline
Overview: Biology’s Most Exciting Era
Concept 1.1 Biologists explore life from the microscopic to the global scale
Concept 1.2 Biological systems are much more than the sum of their parts
1. High-throughput technology. Systems biology depends on methods that can analyze biological materials very quickly and produce enormous amounts of data. An example is the automatic DNA-sequencing machines used by the Human Genome Project.
2. Bioinformatics. The huge databases from high-throughput methods require computing power, software, and mathematical models to process and integrate information.
3. Interdisciplinary research teams. Systems biology teams may include engineers, medical scientists, physicists, chemists, mathematicians, and computer scientists as well as biologists.
Concept 1.3 Biologists explore life across its great diversity of species
Concept 1.4 Evolution accounts for life’s unity and diversity
Concept 1.5 Biologists use various forms of inquiry to explore life
Concept 1.6 A set of themes connects the concepts of biology
The Biology Place – Lab Bench Activity – Cellular Respiration
www.phschool.com ——> go to “The Biology Place” —–> go to LabBench —> go to “Lab 5: Cell Respiration”
1. In this lab activity:
a) You will observe __________________________________________________________________
b) You will investigate ________________________________________________________________
2. Write the equation for cellular respiration:
3. What are the three ways in which you can measure the rate of cellular respiration?
4. Sketch a respirometer and label its important features.
5. As the organism inside the respirometer consumes oxygen, what happens to the water? _________________________
6. What happens to the CO2 that the organism produces? ____________________________
7. Experimental Setup (View the graphic)
a) fill out the table
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Vial 1
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Vial 2
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Vial 3
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Vial 4
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Vial 5
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Vial 6
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| Contents | ||||||
| Temperature |
b) How do you ensure that each vial has an equal volume?
c. What is the purpose of the vial with only glass beads?
8. Analyzing Results
a) What is the equation to determine the rate of respiration?
b) What is X _______________ What is Y _______________
9. Read the respirometers and determine the rate of respiration. Show your calculations

10. Analysis – Self Quiz

a) Describe the relationship between temperature and consumption of oxygen.
b) Calculate the rate of oxygen consumption for germinating corn at 12 degrees. (Show calculations)
c) Based on the graph, would you conclude that non germinating seeds respire?
11. Extension (You do not need the computer to finish this section, do as homework)
A cricket is placed in a respirometer and data taken at three temperatures. The following table shows the data collected.
| Temperatures | |||
| Time (min) | 10 degrees | 18 degrees | 25 degrees |
| 0 | 0.0 | 0.0 | 0.0 |
| 5 | 0.25 | 0.6 | 0.9 |
| 10 | 0.5 | 0.9 | 1.4 |
| 15 | 0.7 | 1.2 | 1.8 |
| 20 | 0.9 | 1.6 | 2.4 |
a ) Graph the data.
b) Determine the rate of respiration for each of the three temperatures. (Show work)
c) Write a paragraph stating your conclusions