A number of mouse models for human cystic fibrosis (CF) exist. Each of these mouse strains is transgenic and bears a different specific CFTR gene mutation. The mutations are the same as those seen in several varieties of human CF. These transgenic CF mice are being used to study the range of different phenotypes that characterize CF in humans. They are also used as models to test potential CF drugs. Unfortunately, most transgenic mouse CF strains do not show one of the most characteristic symptoms of human CF, that of lung congestion. Can you think of a reason why mouse CF strains do not display this symptom of human CF?
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
15. Genomes and Genomics
Genomics and Human Medicine
Problem 27
Textbook Question
Gene targeting and gene editing are both techniques for removing or modifying a particular gene, each of which can produce the same ultimate goal. What is the main technical difference in how DNA is modified that differs between these approaches?
Verified step by step guidance1
Understand that both gene targeting and gene editing aim to modify specific DNA sequences within the genome, but they use different molecular mechanisms to achieve this.
Gene targeting typically relies on homologous recombination, a natural cellular process where a piece of introduced DNA with sequences homologous to the target site replaces or modifies the endogenous gene through crossover events.
Gene editing, on the other hand, often uses engineered nucleases (such as CRISPR-Cas9, TALENs, or ZFNs) to create targeted double-strand breaks (DSBs) at specific genomic locations.
After the DSB is introduced in gene editing, the cell's repair machinery fixes the break either by non-homologous end joining (NHEJ), which can introduce insertions or deletions, or by homology-directed repair (HDR) if a repair template is provided, allowing precise modifications.
Therefore, the main technical difference lies in gene targeting using homologous recombination without necessarily inducing breaks, while gene editing actively induces targeted DNA breaks to stimulate repair pathways for modification.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Gene Targeting
Gene targeting is a technique that uses homologous recombination to introduce specific changes into a gene by replacing or disrupting it with a designed DNA sequence. This method relies on the cell's natural DNA repair mechanisms to incorporate the introduced DNA at a precise location.
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Gene Editing
Gene editing involves directly cutting the DNA at a specific site using engineered nucleases like CRISPR-Cas9, TALENs, or ZFNs, followed by the cell's repair processes to introduce mutations or insertions. It allows precise and efficient modification without necessarily relying on homologous recombination.
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DNA Repair Mechanisms
Cells repair DNA breaks primarily through homologous recombination (HR) or non-homologous end joining (NHEJ). Gene targeting depends on HR for precise DNA replacement, while gene editing often exploits NHEJ or HR after nuclease-induced double-strand breaks to achieve desired modifications.
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