Submission Type
Poster
Start Date
4-26-2023
Abstract
The immune system of the frog Xenopus laevis is similar to humans. MHC Class I is a vital molecule for the immune system of Xenopus laevis. It presents peptides to CD8 T-cells and the presentation of self peptide fragments is crucial for immune self recognition. When MHC Class I presents non-self peptide fragments, it triggers an immune response, causing CD8 T-cells to kill the infected cells. All cells express some level of MHC Class I because all cells can be infected. The role this molecule plays in immune function and self recognition is of particular interest in Xenopus laevis since tadpoles are immunocompetent, yet have undetectable levels of MHC Class I protein (mRNA can be detected in different tissues). MHC Class I protein levels become detectable after metamorphosis and are expressed both as mRNA and protein in adult frogs. We are interested to see if MHC Class I is critical for immune function in Xenopus laevis tadpoles and will investigate by knocking out the MHC Class I gene. To do this, we utilized the CRISPR/Cas9 gene editing tool. Cas9 creates a break in the dsDNA at the location of the gene by using specific guide RNAs, and while the cell attempts to fix its genome multiple insertions and/or deletions can occur in the sequence that inactivates the gene. We generated transgenic tadpoles that have guide RNAs targeting the MHC class I gene. Currently, we are using DNA sequencing to verify successful knockout of the MHC Class I gene.
Recommended Citation
Glasheen, Keely; Marx, David; and Robert, Jacques, "122 - Using CRISPR/Cas9 Genome Editing to Knockout MHC Class I in Xenopus laevis" (2023). GREAT Day Posters. 22.
https://knightscholar.geneseo.edu/great-day-symposium/great-day-2023/posters-2023/22
Included in
122 - Using CRISPR/Cas9 Genome Editing to Knockout MHC Class I in Xenopus laevis
The immune system of the frog Xenopus laevis is similar to humans. MHC Class I is a vital molecule for the immune system of Xenopus laevis. It presents peptides to CD8 T-cells and the presentation of self peptide fragments is crucial for immune self recognition. When MHC Class I presents non-self peptide fragments, it triggers an immune response, causing CD8 T-cells to kill the infected cells. All cells express some level of MHC Class I because all cells can be infected. The role this molecule plays in immune function and self recognition is of particular interest in Xenopus laevis since tadpoles are immunocompetent, yet have undetectable levels of MHC Class I protein (mRNA can be detected in different tissues). MHC Class I protein levels become detectable after metamorphosis and are expressed both as mRNA and protein in adult frogs. We are interested to see if MHC Class I is critical for immune function in Xenopus laevis tadpoles and will investigate by knocking out the MHC Class I gene. To do this, we utilized the CRISPR/Cas9 gene editing tool. Cas9 creates a break in the dsDNA at the location of the gene by using specific guide RNAs, and while the cell attempts to fix its genome multiple insertions and/or deletions can occur in the sequence that inactivates the gene. We generated transgenic tadpoles that have guide RNAs targeting the MHC class I gene. Currently, we are using DNA sequencing to verify successful knockout of the MHC Class I gene.
Comments
Sponsored by Hristina Nedelkovska