New gene editing tool could fix most harmful DNA mutations.

Scientists have raised fresh hopes for treating people with genetic disorders by inventing a powerful new molecular tool that, in principle, can correct the vast majority of mutations that cause human genetic diseases.

The procedure, named “prime editing”, can mend about 89% of the 75,000 or so harmful mutations known to mangle the human genome and lead to conditions such as cystic fibrosis, sickle cell anaemia, and a nerve-destroying illness called Tay-Sachs disease.

The landmark work opens the door to a new era of genome editing, but scientists caution that more research is needed before it can be safely used in humans. Beyond proving its safety, another major hurdle is how to deliver the molecular machinery to cells that need it in sufficient amounts to treat a disorder.

Prime editing

Prime editing can ‘nick’ and replace sections of mutated DNA strands

“This first report of prime editing is the beginning rather than the end of a longstanding aspiration in the life sciences to be able to make any DNA change in any position of a living cell or organism, including potentially human patients with genetic diseases,” said David Liu at the Broad Institute of MIT and Harvard in Cambridge, Massachusetts.

The ability to rewrite the genetic code is one of the most striking scientific advances of recent years. The most common approach, known as Crispr-Cas9, has been likened to “molecular scissors” which home in on a particular DNA sequence and then cut it in two. The procedure allows scientists to disable specific genes and even correct harmful mutations by providing cells with fresh strands of DNA with which to repair the cut.

Crispr-Cas9 is not perfect, however. Often, it leads to cells with a haphazard mix of edits, including extra chunks of DNA called insertions, or missing chunks of genetic code called deletions. These are less of a problem when scientists are working on cells in a dish, because those that are affected can be thrown away. But when genome editing is used to rewrite faulty genes in people’s lungs, hearts and other tissues, far more precision is needed.

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The biggest revolution in gene editing: Crispr-Cas9 explained – video

Andrew Anzalone, also at the Broad Institute, created prime editing with Liu by giving Crispr-Cas9 an overhaul. The new system homes in on its target as before, but instead of chopping the DNA in half, it nicks it, and then writes a new section of DNA into the specified position.

Writing in the journal Nature, the scientists describe how they made 175 different DNA edits to human cells with impressive precision. In one demonstration, they corrected mutations that cause the inherited blood disorder, sickle cell anaemia. In another, they removed the four extra DNA letters in a particular gene that cause Tay-Sachs disease, a rare condition that destroys children’s nerves and usually proves fatal by five years old.

Before prime editing, it was impossible to make such a range of DNA changes in so many different cell types without leaving behind insertions, deletions and other genetic detritus that can interfere with the workings of the edited cell.

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“You can think of prime editors as being like word processors capable of searching for target DNA sequences and precisely replacing them with edited DNA sequences,” Liu said. “Potential impacts include being able to directly correct a much larger fraction of the mutations that cause genetic diseases, and being able to introduce DNA changes into crops that result in healthier or more sustainable foods.”

Robin Lovell-Badge, a geneticist at the Francis Crick Institute in London, said prime editing looked “very exciting” and would be useful for exploring what genes do, making animal models of human genetic disorders, and improving animal and plant agriculture. Because the procedure can make changes that occur naturally in plants, at least some prime-edited crops should not be regulated as “genetically modified”, he added.

But much more work needs to be done before prime editing can be used in humans, Lovell-Badge stressed. “As the authors themselves point out, these are new methods and effort will be needed to develop them to show that they are sufficiently safe and efficient. So far the authors have conducted experiments on just a few human cell types, which is far from being enough.”

While the efficiency of the edits – about 50% in some cases – would be good enough for scientists conducting basic research, he questioned whether it would be useful for scientists working in live animals. “Nevertheless, I am excited about the methods which certainly hold promise and I expect we will see many applications that use these or next generation methods based on them.”

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