I have only worked with an autistic mouse model once and they were nuts. Absolutely adorable, but very difficult to handle. Very interesting video, thanks.
Can you explain why/how CRISPR/Cas9 would be used in conjunction with Cre/LoxP recombination? It seems like both can create knockout mice, so is it not redundant then to use them together?
CRISPR/Cas9 and Cre/LoxP recombination are two distinct genetic engineering tools that serve different purposes in the generation of knockout mice, and they can be used in conjunction for specific applications. While both techniques can be used to create knockout mice, they are not redundant, and their combined use can provide certain advantages. 1. CRISPR/Cas9 for Gene Targeting: Introduction of Mutations: CRISPR/Cas9 technology is commonly used to introduce specific mutations in a target gene. It involves designing a guide RNA (gRNA) that guides the Cas9 enzyme to a specific DNA sequence, where it induces double-strand breaks (DSBs). These DSBs can lead to insertions or deletions (indels) during the repair process, resulting in gene disruption or knockout. 2. Cre/LoxP Recombination: Conditional Knockouts: Cre/LoxP recombination is a tool used to achieve conditional gene knockout. It involves the use of two key elements: Cre recombinase enzyme and LoxP recognition sites. LoxP sites are inserted flanking a gene of interest, and Cre recombinase catalyzes recombination between these sites. This process can lead to the excision of the floxed gene, effectively knocking it out in a tissue-specific or inducible manner. Using both CRISPR/Cas9 and Cre/LoxP recombination together can offer the following advantages: 1. Precise Targeting: CRISPR/Cas9 allows for precise modification of a specific gene at its endogenous locus, ensuring that the mutation is introduced exactly where it's needed. 2. Flexibility: Cre/LoxP recombination enables conditional knockout strategies, allowing researchers to control when and where a gene is disrupted. This is particularly useful for studying genes with essential functions at different stages of development or in specific tissues. 3. Tissue-Specific Knockouts: By combining CRISPR/Cas9 and Cre/LoxP, researchers can create knockout mice with tissue-specific gene disruption. CRISPR/Cas9 is used to introduce LoxP sites or other modifications to the target gene, and Cre recombinase is subsequently expressed under the control of a tissue-specific promoter. 4. Temporal Control: Cre/LoxP allows for temporal control of gene knockout, whereas CRISPR/Cas9 disrupts the gene permanently. This temporal control can be critical for studying genes with complex functions that change over time. In summary, while both CRISPR/Cas9 and Cre/LoxP recombination can be used to create knockout mice, they serve complementary roles. CRISPR/Cas9 is primarily used for precise gene editing, while Cre/LoxP recombination offers conditional and tissue-specific knockout capabilities. Combining these techniques allows researchers to achieve more sophisticated and flexible control over gene knockout experiments, making it a valuable strategy in mouse genetics research.
At 4:55 speaker says: "as there are mulitple cells in the zygote" But this is incorrect! The zygote is the fertilized egg at the one cell stage. Then it is a 2 cell stage embryo, 4 cell stage embryo, 8 cell stage embryo and then morula, blastula, blastocyst. What the speaker is after is that the gene knock out in the genome may not occur at the one cell stage i.e. in the zygote but at a later stage like in the 2 cell stage or 4 cell stage embryo creating a mosaic. Right?
Last year I had mice crewing the wires inside my gas fireplace. I had mice inside the condo walls and I had them LIVING inside my fridge. I could not even imagine why mice were made at all and hated them so much that I didn't really feel bad when they got stuck on glue boards. And now here they are, mice helping cure all disease.
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No mention of Jennifer Doudna?
I have only worked with an autistic mouse model once and they were nuts. Absolutely adorable, but very difficult to handle. Very interesting video, thanks.
Can you explain why/how CRISPR/Cas9 would be used in conjunction with Cre/LoxP recombination? It seems like both can create knockout mice, so is it not redundant then to use them together?
CRISPR/Cas9 and Cre/LoxP recombination are two distinct genetic engineering tools that serve different purposes in the generation of knockout mice, and they can be used in conjunction for specific applications. While both techniques can be used to create knockout mice, they are not redundant, and their combined use can provide certain advantages.
1. CRISPR/Cas9 for Gene Targeting:
Introduction of Mutations: CRISPR/Cas9 technology is commonly used to introduce specific mutations in a target gene. It involves designing a guide RNA (gRNA) that guides the Cas9 enzyme to a specific DNA sequence, where it induces double-strand breaks (DSBs). These DSBs can lead to insertions or deletions (indels) during the repair process, resulting in gene disruption or knockout.
2. Cre/LoxP Recombination:
Conditional Knockouts: Cre/LoxP recombination is a tool used to achieve conditional gene knockout. It involves the use of two key elements: Cre recombinase enzyme and LoxP recognition sites. LoxP sites are inserted flanking a gene of interest, and Cre recombinase catalyzes recombination between these sites. This process can lead to the excision of the floxed gene, effectively knocking it out in a tissue-specific or inducible manner.
Using both CRISPR/Cas9 and Cre/LoxP recombination together can offer the following advantages:
1. Precise Targeting: CRISPR/Cas9 allows for precise modification of a specific gene at its endogenous locus, ensuring that the mutation is introduced exactly where it's needed.
2. Flexibility: Cre/LoxP recombination enables conditional knockout strategies, allowing researchers to control when and where a gene is disrupted. This is particularly useful for studying genes with essential functions at different stages of development or in specific tissues.
3. Tissue-Specific Knockouts: By combining CRISPR/Cas9 and Cre/LoxP, researchers can create knockout mice with tissue-specific gene disruption. CRISPR/Cas9 is used to introduce LoxP sites or other modifications to the target gene, and Cre recombinase is subsequently expressed under the control of a tissue-specific promoter.
4. Temporal Control: Cre/LoxP allows for temporal control of gene knockout, whereas CRISPR/Cas9 disrupts the gene permanently. This temporal control can be critical for studying genes with complex functions that change over time.
In summary, while both CRISPR/Cas9 and Cre/LoxP recombination can be used to create knockout mice, they serve complementary roles. CRISPR/Cas9 is primarily used for precise gene editing, while Cre/LoxP recombination offers conditional and tissue-specific knockout capabilities. Combining these techniques allows researchers to achieve more sophisticated and flexible control over gene knockout experiments, making it a valuable strategy in mouse genetics research.
At 4:55 speaker says: "as there are mulitple cells in the zygote" But this is incorrect! The zygote is the fertilized egg at the one cell stage. Then it is a 2 cell stage embryo, 4 cell stage embryo, 8 cell stage embryo and then morula, blastula, blastocyst. What the speaker is after is that the gene knock out in the genome may not occur at the one cell stage i.e. in the zygote but at a later stage like in the 2 cell stage or 4 cell stage embryo creating a mosaic. Right?
Last year I had mice crewing the wires inside my gas fireplace. I had mice inside the condo walls and I had them LIVING inside my fridge. I could not even imagine why mice were made at all and hated them so much that I didn't really feel bad when they got stuck on glue boards. And now here they are, mice helping cure all disease.
Can this be applied to my wife's Myasthenia Gravis for a cure?
Great
I would like to know what makes you so much jealous of Jenni.....
Synthetic humans 🤔
We became the rats 🧟🧬💉