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Main Authors: Arana, Álvaro J, Veiga-Rua, Sara, Cora, Diego, Gónzalez-Gómez, Manuel A, Seijas, Ana, Carballeda, Maialen, Polo, David, Cuesta, Alberto, Piñeiro, Yolanda, Rivas, José, Novo, Mercedes, Al-Soufi, Wajih, Martínez, Paulino, Sánchez, Laura, Robledo, Diego
Format: Artículo científico
Language:en
Published: International journal of molecular sciences 2025
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/41226739/
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author Arana, Álvaro J
Veiga-Rua, Sara
Cora, Diego
Gónzalez-Gómez, Manuel A
Seijas, Ana
Carballeda, Maialen
Polo, David
Cuesta, Alberto
Piñeiro, Yolanda
Rivas, José
Novo, Mercedes
Al-Soufi, Wajih
Martínez, Paulino
Sánchez, Laura
Robledo, Diego
author_facet Arana, Álvaro J
Veiga-Rua, Sara
Cora, Diego
Gónzalez-Gómez, Manuel A
Seijas, Ana
Carballeda, Maialen
Polo, David
Cuesta, Alberto
Piñeiro, Yolanda
Rivas, José
Novo, Mercedes
Al-Soufi, Wajih
Martínez, Paulino
Sánchez, Laura
Robledo, Diego
Arana, Álvaro J
Veiga-Rua, Sara
Cora, Diego
Gónzalez-Gómez, Manuel A
Seijas, Ana
Carballeda, Maialen
Polo, David
Cuesta, Alberto
Piñeiro, Yolanda
Rivas, José
Novo, Mercedes
Al-Soufi, Wajih
Martínez, Paulino
Sánchez, Laura
Robledo, Diego
collection PubMed - marine biology
contents Comparative Analysis of CRISPR/Cas9 Delivery Methods in Marine Teleost Cell Lines. Arana, Álvaro J Veiga-Rua, Sara Cora, Diego Gónzalez-Gómez, Manuel A Seijas, Ana Carballeda, Maialen Polo, David Cuesta, Alberto Piñeiro, Yolanda Rivas, José Novo, Mercedes Al-Soufi, Wajih Martínez, Paulino Sánchez, Laura Robledo, Diego Animals CRISPR-Cas Systems Gene Editing Cell Line Electroporation Fishes Transfection Gene Transfer Techniques Gene editing technologies such as CRISPR/Cas9 have revolutionized functional genomics, yet their application in marine fish cell lines remains limited by inefficient delivery. This study compares three delivery strategies-electroporation, lipid nanoparticles (LNPs), and magnetofection using gelatin-coated superparamagnetic iron oxide nanoparticles (SPIONs)-for CRISPR/Cas9-mediated editing of the gene in DLB-1 and SaB-1 cell lines. We evaluated transfection and editing efficiency, intracellular Cas9 localization, and genomic stability of the target locus. Electroporation achieved up to 95% editing in SaB-1 under optimized conditions, but only 30% in DLB-1, which exhibited locus-specific genomic rearrangements. Diversa LNPs enabled intracellular delivery and moderate editing (~25%) in DLB-1 but yielded only minimal editing in SaB-1, while SPION-based magnetofection resulted in efficient uptake but no detectable editing, highlighting post-entry barriers. Confocal imaging and fluorescence correlation spectroscopy suggested that nuclear localization and Cas9 aggregation may influence editing success, highlighting the importance of intracellular trafficking in CRISPR/Cas9 delivery. Our findings demonstrate that CRISPR/Cas9 delivery efficiency is cell line-dependent and governed by intracellular trafficking and genomic integrity. These insights provide a practical framework for optimizing gene editing in marine teleosts, advancing both basic research and selective breeding in aquaculture.
format Artículo científico
id pubmed_41226739
institution PubMed
language en
publishDate 2025
publisher International journal of molecular sciences
record_format pubmed
spellingShingle Comparative Analysis of CRISPR/Cas9 Delivery Methods in Marine Teleost Cell Lines.
Arana, Álvaro J
Veiga-Rua, Sara
Cora, Diego
Gónzalez-Gómez, Manuel A
Seijas, Ana
Carballeda, Maialen
Polo, David
Cuesta, Alberto
Piñeiro, Yolanda
Rivas, José
Novo, Mercedes
Al-Soufi, Wajih
Martínez, Paulino
Sánchez, Laura
Robledo, Diego
Animals
CRISPR-Cas Systems
Gene Editing
Cell Line
Electroporation
Fishes
Transfection
Gene Transfer Techniques
Comparative Analysis of CRISPR/Cas9 Delivery Methods in Marine Teleost Cell Lines. Arana, Álvaro J Veiga-Rua, Sara Cora, Diego Gónzalez-Gómez, Manuel A Seijas, Ana Carballeda, Maialen Polo, David Cuesta, Alberto Piñeiro, Yolanda Rivas, José Novo, Mercedes Al-Soufi, Wajih Martínez, Paulino Sánchez, Laura Robledo, Diego Animals CRISPR-Cas Systems Gene Editing Cell Line Electroporation Fishes Transfection Gene Transfer Techniques Gene editing technologies such as CRISPR/Cas9 have revolutionized functional genomics, yet their application in marine fish cell lines remains limited by inefficient delivery. This study compares three delivery strategies-electroporation, lipid nanoparticles (LNPs), and magnetofection using gelatin-coated superparamagnetic iron oxide nanoparticles (SPIONs)-for CRISPR/Cas9-mediated editing of the gene in DLB-1 and SaB-1 cell lines. We evaluated transfection and editing efficiency, intracellular Cas9 localization, and genomic stability of the target locus. Electroporation achieved up to 95% editing in SaB-1 under optimized conditions, but only 30% in DLB-1, which exhibited locus-specific genomic rearrangements. Diversa LNPs enabled intracellular delivery and moderate editing (~25%) in DLB-1 but yielded only minimal editing in SaB-1, while SPION-based magnetofection resulted in efficient uptake but no detectable editing, highlighting post-entry barriers. Confocal imaging and fluorescence correlation spectroscopy suggested that nuclear localization and Cas9 aggregation may influence editing success, highlighting the importance of intracellular trafficking in CRISPR/Cas9 delivery. Our findings demonstrate that CRISPR/Cas9 delivery efficiency is cell line-dependent and governed by intracellular trafficking and genomic integrity. These insights provide a practical framework for optimizing gene editing in marine teleosts, advancing both basic research and selective breeding in aquaculture.
title Comparative Analysis of CRISPR/Cas9 Delivery Methods in Marine Teleost Cell Lines.
topic Animals
CRISPR-Cas Systems
Gene Editing
Cell Line
Electroporation
Fishes
Transfection
Gene Transfer Techniques
url https://pubmed.ncbi.nlm.nih.gov/41226739/