Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
18. Molecular Genetic Tools
Genetic Cloning
4:47 minutes
Problem 7c
Textbook Question
Textbook QuestionUsing animal models of human diseases can lead to insights into the cellular and genetic bases of the diseases. Duchenne muscular dystrophy (DMD) is the consequence of an X-linked recessive allele. How would you make a mouse model of DMD?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
X-linked Recessive Inheritance
X-linked recessive inheritance refers to a pattern where a gene causing a trait or disorder is located on the X chromosome. Males, having one X and one Y chromosome, are more likely to express X-linked recessive traits because they have only one copy of the X chromosome. In contrast, females have two X chromosomes, so they can be carriers without showing symptoms if they have one normal allele.
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Mouse Models in Genetics
Mouse models are genetically modified mice used to study human diseases. They allow researchers to investigate the genetic, cellular, and physiological aspects of diseases in a controlled environment. By creating specific mutations in mice that mimic human conditions, scientists can observe disease progression and test potential treatments, providing valuable insights into the underlying mechanisms.
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Gene Editing Techniques
Gene editing techniques, such as CRISPR-Cas9, enable precise modifications of an organism's DNA. In the context of creating a mouse model for Duchenne muscular dystrophy, researchers can use these techniques to introduce mutations that replicate the disease-causing allele. This allows for the study of disease mechanisms and the evaluation of therapeutic strategies in a living organism.
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