Scientists have made a major breakthrough in genetic engineering by creating optimized prime genes in mice. This breakthrough is especially significant as it could pave the way for treatments of human diseases, such as cancer. The research team was able to optimize the prime genes of mice by utilizing a synthetic gene-editing tool called CRISPR/Cas9. This tool allowed the team to effectively edit out any faulty genes, while creating an optimal set of prime genes. Additionally, this technology could also be used to create gene therapies for humans, which could help to treat a variety of diseases. This breakthrough could have significant implications for the future of medicine and could help to improve the quality of life for many people.

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source: Phys.org