US8697359B1: CRISPR-Cas systems and methods for altering expression of gene products. Broad Institute; Massachusetts Institute of Technology (inventor Feng Zhang). Filed 2013, granted 2014. Status: Granted (active).
US20140068797A1: Methods and compositions for RNA-directed target DNA modification and for RNA-directed modulation of transcription. As listed on Google Patents: University of California; University of Vienna (inventors Jennifer A. Doudna, Martin Jinek, Emmanuelle Charpentier and others). Filed 2013, granted 2019. Status: Application published 2014; granted 2019 as US10266850B2 (active).
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Esvelt and colleagues discussed using CRISPR gene drives to change wild populations, and safeguards.
As reported in: Esvelt, Smidler, Catteruccia et al. (2014). Concerning RNA-guided gene drives for the alteration of wild populations. eLife. doi:10.7554/eLife.03401
Jinek and colleagues showed Cas9 can be programmed with RNA to cut chosen DNA, work honored with the 2020 Nobel Prize in Chemistry.
As reported in: Jinek, Chylinski, Fonfara et al. (2012). A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity. Science. doi:10.1126/science.1225829
Gantz and colleagues built an efficient Cas9 gene drive in Anopheles stephensi.
As reported in: Gantz, Jasinskiene, Tatarenkova et al. (2015). Highly efficient Cas9-mediated gene drive for population modification of the malaria vector mosquito Anopheles stephensi. Proceedings of the National Academy of Sciences. doi:10.1073/pnas.1521077112
Hammond and colleagues built a gene drive targeting female fertility in Anopheles gambiae.
As reported in: Hammond, Galizi, Kyrou et al. (2016). A CRISPR-Cas9 gene drive system targeting female reproduction in the malaria mosquito vector Anopheles gambiae. Nature Biotechnology. doi:10.1038/nbt.3439