Table of contents
- 1. Introduction to Biology2h 40m
- 2. Chemistry3h 40m
- 3. Water1h 26m
- 4. Biomolecules2h 23m
- 5. Cell Components2h 26m
- 6. The Membrane2h 31m
- 7. Energy and Metabolism2h 0m
- 8. Respiration2h 40m
- 9. Photosynthesis2h 49m
- 10. Cell Signaling59m
- 11. Cell Division2h 47m
- 12. Meiosis2h 0m
- 13. Mendelian Genetics4h 41m
- Introduction to Mendel's Experiments7m
- Genotype vs. Phenotype17m
- Punnett Squares13m
- Mendel's Experiments26m
- Mendel's Laws18m
- Monohybrid Crosses16m
- Test Crosses14m
- Dihybrid Crosses20m
- Punnett Square Probability26m
- Incomplete Dominance vs. Codominance20m
- Epistasis7m
- Non-Mendelian Genetics12m
- Pedigrees6m
- Autosomal Inheritance21m
- Sex-Linked Inheritance43m
- X-Inactivation9m
- 14. DNA Synthesis2h 27m
- 15. Gene Expression3h 20m
- 16. Regulation of Expression3h 31m
- Introduction to Regulation of Gene Expression13m
- Prokaryotic Gene Regulation via Operons27m
- The Lac Operon21m
- Glucose's Impact on Lac Operon25m
- The Trp Operon20m
- Review of the Lac Operon & Trp Operon11m
- Introduction to Eukaryotic Gene Regulation9m
- Eukaryotic Chromatin Modifications16m
- Eukaryotic Transcriptional Control22m
- Eukaryotic Post-Transcriptional Regulation28m
- Eukaryotic Post-Translational Regulation13m
- 17. Viruses37m
- 18. Biotechnology2h 58m
- 19. Genomics17m
- 20. Development1h 5m
- 21. Evolution3h 1m
- 22. Evolution of Populations3h 52m
- 23. Speciation1h 37m
- 24. History of Life on Earth2h 6m
- 25. Phylogeny2h 31m
- 26. Prokaryotes4h 59m
- 27. Protists1h 12m
- 28. Plants1h 22m
- 29. Fungi36m
- 30. Overview of Animals34m
- 31. Invertebrates1h 2m
- 32. Vertebrates50m
- 33. Plant Anatomy1h 3m
- 34. Vascular Plant Transport2m
- 35. Soil37m
- 36. Plant Reproduction47m
- 37. Plant Sensation and Response1h 9m
- 38. Animal Form and Function1h 19m
- 39. Digestive System10m
- 40. Circulatory System1h 57m
- 41. Immune System1h 12m
- 42. Osmoregulation and Excretion50m
- 43. Endocrine System4m
- 44. Animal Reproduction2m
- 45. Nervous System55m
- 46. Sensory Systems46m
- 47. Muscle Systems23m
- 48. Ecology3h 11m
- Introduction to Ecology20m
- Biogeography14m
- Earth's Climate Patterns50m
- Introduction to Terrestrial Biomes10m
- Terrestrial Biomes: Near Equator13m
- Terrestrial Biomes: Temperate Regions10m
- Terrestrial Biomes: Northern Regions15m
- Introduction to Aquatic Biomes27m
- Freshwater Aquatic Biomes14m
- Marine Aquatic Biomes13m
- 49. Animal Behavior28m
- 50. Population Ecology3h 41m
- Introduction to Population Ecology28m
- Population Sampling Methods23m
- Life History12m
- Population Demography17m
- Factors Limiting Population Growth14m
- Introduction to Population Growth Models22m
- Linear Population Growth6m
- Exponential Population Growth29m
- Logistic Population Growth32m
- r/K Selection10m
- The Human Population22m
- 51. Community Ecology2h 46m
- Introduction to Community Ecology2m
- Introduction to Community Interactions9m
- Community Interactions: Competition (-/-)38m
- Community Interactions: Exploitation (+/-)23m
- Community Interactions: Mutualism (+/+) & Commensalism (+/0)9m
- Community Structure35m
- Community Dynamics26m
- Geographic Impact on Communities21m
- 52. Ecosystems2h 36m
- 53. Conservation Biology24m
29. Fungi
Fungi
2:39 minutes
Problem 9a
Textbook Question
Textbook QuestionA particular cell type spends 4 hours in G1 phase, 2 hours in S phase, 2 hours in G2 phase, and 30 minutes in M phase. If a pulse–chase experiment were performed with radioactive thymidine on an asynchronous culture of such cells, what percentage of mitotic cells would be radiolabeled 9 hours after the pulse? a. 0 percent b. 50 percent c. 75 percent d. 100 percent
Verified step by step guidance
1
Step 1: Understand the problem. The question is asking for the percentage of mitotic cells that would be radiolabeled 9 hours after the pulse in a pulse-chase experiment. This experiment involves labeling cells with a radioactive marker (in this case, thymidine) and then following the marker through the cell cycle.
Step 2: Calculate the total cell cycle time. The cell spends 4 hours in G1 phase, 2 hours in S phase, 2 hours in G2 phase, and 30 minutes (or 0.5 hours) in M phase. So, the total cell cycle time is 4 + 2 + 2 + 0.5 = 8.5 hours.
Step 3: Determine the time when the cells are labeled. The cells are labeled with radioactive thymidine during the S phase, which is 4 hours into the cell cycle. Therefore, cells that were in the S phase at the time of the pulse will be in the M phase 4.5 hours later (2 hours for the rest of S phase, 2 hours for G2 phase, and 0.5 hours for M phase).
Step 4: Calculate the time after the pulse when the cells are in the M phase. The cells are in the M phase 4.5 hours after the pulse. Therefore, 9 hours after the pulse, two cell cycles have passed and the cells are again in the M phase. This means that all cells that were in the S phase at the time of the pulse and survived two cell cycles are now in the M phase and are radiolabeled.
Step 5: Answer the question. Therefore, 100 percent of the mitotic cells would be radiolabeled 9 hours after the pulse.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Cell Cycle Phases
The cell cycle consists of several phases: G1 (gap 1), S (synthesis), G2 (gap 2), and M (mitosis). Each phase has a specific duration and function, with G1 being the growth phase, S phase involving DNA replication, G2 preparing for mitosis, and M being the actual division of the cell. Understanding the timing of these phases is crucial for determining how long cells spend in each stage and how this affects the overall cycle.
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Pulse-Chase Experiment
A pulse-chase experiment is a technique used to study the dynamics of cellular processes, such as DNA synthesis. In this method, cells are exposed to a labeled compound (the pulse) for a short time, followed by a period without the label (the chase). This allows researchers to track the incorporation of the label into cellular components over time, providing insights into the timing of processes like DNA replication and cell division.
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Radiolabeling and Mitotic Cells
Radiolabeling refers to the incorporation of a radioactive isotope into a molecule, such as thymidine, which is used to label newly synthesized DNA. In the context of the cell cycle, only cells that have undergone DNA replication during the S phase will be radiolabeled. By calculating the time spent in each phase, one can determine the percentage of cells that are mitotic and have incorporated the label after a given time, which is essential for answering the question.
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