The definitive guide to gene editing.
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Technology · Large-cargo editing

Transposases

Enzymes that cut a segment of DNA out of one place and paste it into another — nature's own copy-and-paste.

Phase I/II DNAlarge insertions
Clinical research Being tested in people in registered clinical trials. Being in trials is not evidence that a treatment works or is safe.

Simple explanation

Transposons are stretches of DNA that move themselves around the genome; roughly half of human DNA descends from them. Their moving machinery has been domesticated: load a therapeutic gene into a transposon and the transposase will paste the whole cassette into a cell's DNA. The catch is aim — left to themselves, they land in many places, and where they land matters.

Go deeper

DNA transposases such as Sleeping Beauty and piggyBac excise a cargo flanked by inverted terminal repeats and integrate it into the genome, carrying multi-kilobase payloads without viral vectors. Integration is semi-random with sequence preferences, raising insertional-mutagenesis concerns. CRISPR-associated transposases (CASTs), found in Vibrio and Scytonema species, couple transposition to RNA-guided targeting and are an active engineering effort aimed at giving transposases an address.

Where they are used

Non-viral CAR-T manufacturing is the most established clinical application: Sleeping Beauty and piggyBac provide a cheaper alternative to viral vectors for inserting a chimeric antigen receptor. Insertional mutagenesis remains the safety question the field takes most seriously, and long-term follow-up of transposon-engineered cell products is an active area of surveillance.

Where they are used
A cassette of sequence being lifted from one strand and set into another. Illustration generated for The CRISPR Atlas — a visual aid, not a photograph or a literal depiction of molecular structure.

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Educational information only This page is a reference, not medical advice. Research and regulatory status change; check the last-updated date above and confirm anything important against the primary sources listed.