March 2020
Having fixated on the notion that the DNA sequence which forms a gene will be expressed as a specific protein, biotech scientists were then convinced that, if they disrupted a tiny part of that DNA sequence, the cell's ability to generate the protein would be lost.
Enter 'CRISPR', a molecular device which can be engineered to latch onto a very specific section of the genome and induce a small localised disruption in the DNA [1]. This provided scientists with a simple means to 'knock out' a gene.
However, a year ago, a paper was published which reported that, while CRISPR did, indeed, knock out the planned gene, the damaged DNA could still code for a protein in 50% of the cells analysed, albeit a different one [2].
Since then, another team has taken a closer look at what was actually emerging from knocked out genes.