CRISPR Cas9 explained. CRISPR (clustered regularly interspaced short palindromic repeats) are segments of prokaryotic DNA containing short repetitions of base sequences. is an RNA-guided gene-editing platform that makes use of a bacterially derived protein (Cas9) and a synthetic guide RNA to introduce a double strand break at a specific location within the genome.
Cas9 is an enzyme that snips DNA, and CRISPR is a collection of DNA sequences that tells Cas9 exactly where to snip.
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The University of California announced today that the U.S. Patent and Trademark Office has granted U.S. Patent Number 10,113,167, covering unique RNA guides that, when combined with the Cas9 protein, are effective at homing in on and editing genes. These RNA/protein combinations act like precision-targeted gene-editing scissors.
The Rockefeller University has announced that Jennifer Doudna will receive this year's Pearl Meister Greengard Prize, a major international accolade honoring outstanding women scientists.
Part of the 2017 Berkeley Summer Reading List
Jennifer Doudna, professor and co-inventor of CRISPR-Cas9 gene editing, speaks with Susan Koskinen, head of the Life and Health Sciences Library Division