Researchers in China have used a new method to produce
genetically modified monkeys. Their
purpose is to advance medical research by creating monkeys genetically
predisposed to develop human diseases.
But the new method is so precise and so successful that one might
imagine it leading to genetically modified humans.
Caption: Researchers achieved precise gene modification in
monkeys. Credit: Cell, Niu et al.
According to a report published in the January 30 issue of the journal Cell, scientists used a new gene editing technique known as the CRISPR/Cas9 system. The technique allows for very precisely targeted modification of DNA sequences.
It also allows researchers to trigger more than one modification at a time. And it seems to avoid causing extraneous mutations where they are not wanted.
With the CRISPR/Cas9 technique, researchers edited the DNA in monkey embryos at the one-cell stage. As that cell multiplied, all the cells of the body contained the gene edits, probably including the cells the newborn monkeys might someday pass to their descendants. In other words, this is precise germline genetic engineering in primates.
"Our study shows that the CRISPR/Cas9 system enables simultaneous disruption of two target genes in one step without producing off-target mutations," claimed Jiahao Sha, one of the lead authors at Nanjing Medical University.
The goal for now, Sha said, is to refine the technique and to be able to create "many disease models...in monkeys," according to the press release issued by the journal Cell.
Just how refined will the technique become? Consider that the first successful germline modified monkey was only reported in 2001. The current advance offers far more precision. With enough precision, it might become possible to apply this technique to a single-cell human egg.
The modification could be verified before the embryo is implanted, using the well-established technique of pre-implantation genetic diagnosis or PGD. If implanted and brought to term, the human life created this way would have its germline DNA modified, meaning that the modification would pass to future generations.
No one knows now whether this technique will offer the kind of precision that would be required to move from monkeys to humans. But just how much precision is, in fact, required? With PGD as a way to catch any "mistakes," might ethics committees, in a few decades or even sooner, permit couples and researchers to use this technique in order to avoid transmitting genetic problems to future generations? Will it then be used to add something new or desirable to the genetic inheritance of our offspring?
The article, Niu et al., "Generation of gene-modified cynomolgus monkey via Cas9/RNA-mediated gene targeting in one-cell embryos," is published in the January 30, 2014 issue of Cell.
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