Effect of CRISPR/Cas9 Targets Associated with Iron Metabolism and Its Variation on Transcriptional Regulation of SHK-1 Cell Line as a Model for Iron Metabolism
Phillip Dettleff,
Yehwa Jin,
Carolina Peñaloza,
Rodrigo Pulgar,
Alejandro Sáez,
Diego Robledo,
Sebastian Escobar-Aguirre
Affiliations
Phillip Dettleff
Escuela de Medicina Veterinaria, Facultad de Agronomía y Sistemas Naturales, Facultad de Ciencias Biológicas y Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago 8320165, Chile
Yehwa Jin
The Center for Aquaculture Technologies, San Diego, CA 92121, USA
Carolina Peñaloza
Benchmark Genetics, Roslin Innovation Centre, The University of Edinburgh, Easter Bush Campus, Midlothian EH25 9RG, Edinburgh, UK
Rodrigo Pulgar
Laboratorio de Genómica y Genética de Interacciones Biológicas (LG2IB), Instituto de Nutrición y Tecnología de los Alimento, Universidad de Chile, Santiago 7810000, Chile
Alejandro Sáez
Laboratorio Biotecnología Molecular Marina, Facultad de Agronomía y Sistemas Naturales, Pontificia Universidad Católica de Chile, Santiago 8320165, Chile
Diego Robledo
The Roslin Institute and Royal (Dick) School of Veterinary Studies, The University of Edinburgh, Edinburgh EH8 9YL, UK
Sebastian Escobar-Aguirre
Laboratorio Biotecnología Molecular Marina, Facultad de Agronomía y Sistemas Naturales, Pontificia Universidad Católica de Chile, Santiago 8320165, Chile
In this study, we investigated the function of a gene associated with iron metabolism using CRISPR-Cas9 and RNA sequencing in SHK-1 salmon cells. Our objective was to understand how different guide RNA (gRNA) sequences against the transferrin gene tf could influence gene expression and cellular processes related to iron uptake. RNA-Seq analysis was performed to evaluate the transcriptomic effects of two distinct gRNA targets with high knock-out (KO) efficiencies for the targeted tf gene in the SHK-1 genome. Our results showed no significant differential expression in transferrin-related transcripts between wild-type and CRISPR-edited cells; however, there were major differences between their transcriptomes, indicating complex transcriptional regulation changes. Enrichment analysis highlighted specific processes and molecular functions, including those related to the nucleus, cytoplasm, and protein binding. Notably, different sgRNAs targeting tf might result in different mutations at DNA levels in SHK-1 salmon cells.