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Crispr-Cas9

9 GoKawiil briefs on this topic

Intellia's in-body CRISPR therapy shows lasting effect after four years

Intellia Therapeutics has released four-year follow-up data showing its gene-editing therapy lonvoguran ziclumeran continues to suppress a protein that triggers hereditary angioedema attacks. The treatment uses CRISPR-Cas9 delivered directly into the body to disable the gene producing prekallikrein, rather than editing cells outside the body as with existing therapies. Intellia has filed for FDA approval, with a decision expected by 10 March.

Study identifies rice protein NVR1 that detects insect salivary signal 2′,3′-cNMP

Researchers studying rice and the stink bug Nezara viridula found that insect saliva deposited during feeding contains a small signalling molecule, 2′,3′-cNMP, produced by salivary effector proteins. They identified a plant RNA-binding protein, NVR1, that senses this molecule and used CRISPR knockouts and overexpression lines in rice and Nicotiana benthamiana, alongside related GRP7/GRP8 genes, to probe how plants detect insect attack at the molecular level.

Prime Medicine edits human DNA inside the body for first time in Wilson disease trial

Prime Medicine has treated the first patient in a clinical trial using prime editing, a precise gene-editing technique, to correct a mutation in liver cells directly inside the body. The target is Wilson disease, caused by mutations in the ATP7B gene that leave excess copper to build up and damage the liver and nervous system. The company says it expects to report initial trial results next year.

Study links chronic cellular stress response to Angelman syndrome symptoms in mice

Researchers at Washington University in St. Louis used Ube3a-deficient mice, a standard model of Angelman syndrome, along with a newly engineered Asns-mutant mouse line, to study neuronal stress signaling. They report that sustained activation of a cellular stress pathway in neurons contributes to the behavioral and neurological phenotypes seen in the Angelman mouse model.

Tropic wins UK approval path for CRISPR-edited non-browning banana

Norwich-based Tropic has developed a gene-edited banana that resists browning for an extra day or two after peeling, using CRISPR-Cas9 to suppress three copies of the gene behind the polyphenol oxidase enzyme. CEO Gilad Gershon said the fruit is already grown in Latin America and has regulatory approval in 10 countries including Japan, Brazil and the Philippines, and is now nearing UK supermarket shelves.

New gene-editing tools aim to move beyond CRISPR-Cas9's limits

Researchers, including Ying Zhang at Wuhan University and Shannon Miller at Scripps Research, are developing a range of genome-editing technologies that go beyond standard CRISPR-Cas9, some building on it and others operating independently. These newer methods are designed to insert or replace larger stretches of DNA, a task CRISPR-Cas9 struggles with, though the field remains in early stages.

Anthropic Says Claude AI Spotted an Unknown CRISPR-Like Enzyme System

Anthropic reported that its Claude AI model identified a previously undocumented enzyme system that structurally resembles the Cas9 protein used in CRISPR gene editing. The company acknowledged it cannot yet confirm what functions the newly flagged system actually performs.

St. Jude study finds blocking ZMYND8 protein restores exhausted T cell function

Researchers at St. Jude Children's Research Hospital used CRISPR-Cas9 screening in mouse T cell models to identify ZMYND8 as a regulator of T cell exhaustion. Removing ZMYND8 boosted IL-2 signalling in antigen-specific CD8+ T cells, including those engineered with CAR constructs, helping the cells retain function against tumours in mouse models.

Cohesin complex found to remodel DNA contacts at stalled replication forks

Researchers using engineered HCT116 cell lines with degradable cohesin components (RAD21, WAPL, CTCF) and SMARCAL1 showed that cohesin actively reorganizes chromatin contacts around replication forks. This reshaping helps slow down forks and promotes their reversal when replication stress occurs, linking genome organization machinery directly to DNA replication control.