CRISPR technology uses the DNA-cutting enzyme Cas9, with the help of a guide RNA sequence, to find and modify genetic targets. Scientists can easily engineer multiple new guide RNAs using standard molecular biology techniques. This makes for a much faster and efficient method to modify the genome of any cell type in any species.
The team found that a remarkable 50 of 52 guide RNAs tested successfully cut both copies of the genes. The extremely high success rate for these engineered guide RNAs seems to be consistent across many cell types, which led them to create a library of guide RNAs targeting every gene in the mouse genome.
“CRISPR technology is revolutionising how we study the behaviour of cells,” says Dr Kosuke Yusa, lead author from the Wellcome Trust Sanger Institute. “We’ve developed a thorough library that can be used by other researchers to study the role of any gene. We can create a library of this type for any cell or any species.”
Read more at: MedicalXpress