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
13. Mendelian Genetics
Sex-Linked Inheritance
0:27 minutes
Problem 12
Textbook Question
Textbook QuestionWhy do more men than women have colorblindness?
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1
Understand the genetic basis of colorblindness: Colorblindness is primarily caused by mutations in the genes that are responsible for the production of photopigments in the cone cells of the retina. These genes are located on the X chromosome.
Recognize the difference in genetic inheritance between males and females: Males have one X chromosome and one Y chromosome (XY), while females have two X chromosomes (XX).
Consider the impact of having only one X chromosome in males: In males, the presence of a mutation in the only X chromosome will result in colorblindness because there is no second X chromosome to potentially provide a normal copy of the gene.
Examine the inheritance in females: Females must inherit two copies of the mutated gene (one from each parent) to exhibit colorblindness. If they inherit only one mutated gene, the normal gene on the other X chromosome can compensate, typically preventing the development of colorblindness.
Conclude why colorblindness is more common in males: Since males are hemizygous for the X chromosome (having only one X chromosome), any mutation on it expresses the trait of colorblindness. Females, having two X chromosomes, are less likely to be affected as they would require mutations in both copies of the gene.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
X-Linked Inheritance
Colorblindness is primarily caused by mutations in genes located on the X chromosome. Since men have one X and one Y chromosome, a single mutated gene on their X chromosome will result in colorblindness. In contrast, women have two X chromosomes, so a mutation must occur in both to express the condition, making it less common among females.
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X-Linked Inheritance
Genetic Mutation
Colorblindness is often the result of genetic mutations that affect the photopigments in the retina, which are responsible for color perception. These mutations can alter the way light is absorbed by the cones in the eyes, leading to difficulties in distinguishing certain colors, particularly red and green.
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Mutations
Prevalence and Population Genetics
The prevalence of colorblindness varies between genders due to the genetic mechanisms involved. Statistically, about 8% of men and only about 0.5% of women are affected by colorblindness, illustrating how X-linked traits can lead to significant differences in expression between sexes in a population.
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Mendelian and Population Genetics
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