CRISPR editing might stop HIV

| | June 10, 2014
This article or excerpt is included in the GLP’s daily curated selection of ideologically diverse news, opinion and analysis of biotechnology innovation.

Take a hot new method that’s opened up a new era of genetic engineering, apply it to the wonder stem cells that in 2012 won their discoverer a Nobel prize, and you might just have a tool to cure HIV infection.

That’s the hope of researchers led by Yuet Kan of the University of California, San Francisco – and they have proved the basic principle, altering the genome of induced pluripotent stem cells (iPSCs) to give them a rare natural mutation that allows some people to resist HIV.

Kan’s work relies on “genome editing” – snipping out a particular DNA sequence and replacing it with another. It’s much more precise than traditional forms of genetic engineering, in which sequences are added to the genome at random locations.

To alter the stem cells, Kan’s team turned to the CRISPR-Cas9 system, a super-efficient method of genome editing based on an ancient bacterial “immune system”. In bacteria, the system takes fragments of DNA from invading viruses and splices them into the cell’s own DNA, where they act like “wanted” posters, allowing the viruses to be recognised and attacked in future.

Read the full, original story: Gene editing tool can write HIV out of the picture

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