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
3: minutes
Problem 8
Textbook Question
Textbook QuestionDescribe how CRISPR–Cas has been modified to create a genome-editing tool.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
CRISPR-Cas System
The CRISPR-Cas system is a natural defense mechanism found in bacteria that protects against viral infections. It consists of CRISPR sequences, which store segments of viral DNA, and Cas proteins that can cut DNA. This system has been harnessed for genome editing, allowing precise modifications to DNA in various organisms.
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Genomic Variation
Genome Editing
Genome editing refers to the techniques used to alter the genetic material of an organism. CRISPR-Cas9 is one of the most prominent methods, enabling targeted changes to DNA sequences. This technology has applications in medicine, agriculture, and research, facilitating the study of gene function and the development of genetically modified organisms.
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Modifications of CRISPR-Cas
Modifications to the CRISPR-Cas system have enhanced its specificity and efficiency for genome editing. These include engineering Cas proteins to improve their targeting accuracy, developing new delivery methods for CRISPR components, and creating variations like CRISPR-Cas12 and Cas13, which can target RNA. Such advancements expand the potential applications of CRISPR technology in various fields.
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