Knocking Out the Plant-specific FLS2 Immune Receptor in Tobacco Using CRISPR/Cas9
Knocking Out the Plant-specific FLS2 Immune Receptor in Tobacco Using CRISPR/Cas9
About Me
My name is Zoe Turk, and I’m a pre-nursing Biology major from California. I love all things human biology, but I’m also interested in more general genetics and interactions between cells. Outside of school, I like to read, sew, put together outfits, and go to concerts.
Abstract
Due to their inability to produce antibodies, plants use solely innate mechanisms to fight pathogens. Cell surface receptors detect pathogenic patterns (pattern-triggered immunity), and intracellular receptors respond to pathogenic effectors (effector-triggered immunity). FLS2, a pattern-detecting immune receptor in some angiosperms, detects a 22 amino acid sequence (flg22) in bacterial flagellin and initiates an immune response against the potential bacterial pathogen. Our project knocked out the FLS2 gene in tobacco plants using CRISPR/Cas9, a “molecular scissors” bacterial DNA adaptive immune system co-opted by biologists to excise specific genes. The long-term reasoning for this knockout is to use it as a complementation system to transiently express FLS2 from other flowering plants (that may be better at recognizing various pathogens) in tobacco. The goal is to restore the wild-type PTI phenotype and better understand how the plant immune system evolved.