In a new study published in Nature Communications, researchers have used a combination of biochemical and structural approaches to map out the precise transcript of CRISPR-Cas9 complexes. The team has identified a novel structure of the CRISPR-Cas9 complex that can be used to target specific DNA sequences with unprecedented accuracy. This could lead to new treatments for genetic diseases and potentially revolutionize gene editing. This breakthrough could also enable scientists to study gene regulation in a more precise and efficient way.

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source: Phys.org