2015
DOI: 10.1126/science.aad1191
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Genome-wide inactivation of porcine endogenous retroviruses (PERVs)

Abstract: Virally cleansing the pig genome Transplants from pigs could be a solution to a shortage of human organs for transplantation. Unfortunately, porcine endogenous retroviruses (PERVs) are rife in pigs and can be transmitted to humans, risking disease. L. Yang et al. integrated CRISPR-Cas into the pig cell genome, where continuous induction of the Cas9 editing enzyme resulted in the mutation of every single PERV reverse transcriptase gene. This prevented replication o… Show more

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Cited by 531 publications
(418 citation statements)
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“…This has enabled, for example, the creation of liver tumors by direct injection of CRISPR/Cas9 to delete Pten and p53 in the same cells [19]. This method has been used to disrupt as many as 62 endogenous retrovirus loci, which pose potential risks in clinical application, in order to generate pigs that are safe to use in pig-to-human xenotransplantation [20].…”
Section: Application Of Crispr/cas9mentioning
confidence: 99%
“…This has enabled, for example, the creation of liver tumors by direct injection of CRISPR/Cas9 to delete Pten and p53 in the same cells [19]. This method has been used to disrupt as many as 62 endogenous retrovirus loci, which pose potential risks in clinical application, in order to generate pigs that are safe to use in pig-to-human xenotransplantation [20].…”
Section: Application Of Crispr/cas9mentioning
confidence: 99%
“…In our lifetime, we may see foods or pets customized and marketed to suit individual's whims. Researchers have already proposed using CRISPR to modify pigs to develop human-compatible organs (Yang et al 2015). CRISPR could also be used to genetically modify domestic pets to be more appealing to humans.…”
Section: Revolutionary Social Impactmentioning
confidence: 99%
“…Additionally, it will The humanization of mice and larger animals such as cattle, pigs, and cats will be streamlined by efficient orthologous gene(s) KO using genome editing, and the generation of various humanized Tc animal models may promote drug development and therapy [102][103][104]. Once HACs/MACs with gene(s) of interest are constructed, they can be transferred to various mammalian cells and maintained independently without integration into the host genome.…”
Section: Conclusion and Future Perspectivesmentioning
confidence: 99%