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CRISPR-Cas9 variants, key to overcoming major limitation in gene editing system

Entire genome now targetable, open to interventions for use in combating diseases

31-Mar-2020

Key points from article :

CRISPR-Cas9, modified, now less dependent on protospacer adjacent motif (PAM).

Overcoming that limitation, allowing them to target any location on entire genome.

Team created variants of Cas9 protein not requiring specific PAM to bind to and cut DNA.

Two variants created, SpG and SpRY, more efficient than regular Cas9 enzyme.

New approach allows targeting of previously inaccessible regions of the genome.

Next step, develop deeper understanding of mechanisms involved in Cas9 protein variants.

Researchers from Massachusetts General Hospital, published in Science.

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Massachusetts General Hospital (MGH)

Largest teaching hospital of Harvard Medical School located in Boston

Science Magazine

Academic journal of the American Association for the Advancement of Science (AAAS) and one of the world's top academic journals

Topics mentioned on this page:
Gene Therapy