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
- Genetic Cloning
  9m
- Methods for Analyzing DNA
  9m
19. Cancer Genetics29m
- Overview of Cancer
  21m
- Cancer Mutations
  7m
20. Quantitative Genetics1h 26m
21. Population Genetics50m
- Hardy Weinberg
  19m
- Allelic Frequency Changes
  31m
22. Evolutionary Genetics29m

15. Genomes and Genomics

Genomics and Human Medicine

Genetics

15. Genomes and Genomics

Genomics and Human Medicine

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Problem 8

Textbook Question

Describe how CRISPR–Cas has been modified to create a genome-editing tool.

Verified step by step guidance

Understand the natural function of CRISPR–Cas: CRISPR–Cas is a bacterial immune system that uses RNA-guided Cas proteins to target and cut foreign DNA, such as that from viruses, based on sequence complementarity.

Identify the key components of CRISPR–Cas: The system has two main components—(1) the guide RNA (gRNA), which is designed to match the target DNA sequence, and (2) the Cas9 protein, which acts as molecular scissors to cut the DNA at the target site.

Explain how scientists modified CRISPR–Cas: Researchers adapted the system by engineering the guide RNA to target specific DNA sequences of interest in the genome, allowing precise targeting of genes for editing.

Describe the genome-editing process: Once the Cas9 protein cuts the DNA at the target site, the cell's natural DNA repair mechanisms are used to introduce changes. Non-homologous end joining (NHEJ) can create insertions or deletions, while homology-directed repair (HDR) can introduce specific sequences if a repair template is provided.

Highlight the versatility of CRISPR–Cas: The system has been further modified to include 'dead' Cas9 (dCas9) for gene regulation, base editors for single-nucleotide changes, and prime editing for more precise edits, making it a powerful and versatile 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 by allowing precise modifications to DNA in various organisms.

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 tools for genome editing, enabling researchers to add, delete, or modify specific DNA sequences. This technology has vast applications in medicine, agriculture, and biological research.

Modifications of CRISPR-Cas

Modifications to the CRISPR-Cas system have enhanced its specificity and efficiency for genome editing. These include the development of Cas9 variants with altered cutting properties, the use of guide RNA to improve targeting accuracy, and the creation of CRISPR systems that can edit RNA instead of DNA. Such advancements have broadened the potential applications of CRISPR technology.

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