China did it once again


Junjiu Huang is back. Two years later, Protein & Cell publishes another study by the team which first edited human embryos in 2015 sparking uproar. They targeted the gene responsible for beta thalassemia, once again. This time, however, in place of using embryos discarded by fertilization clinics, they resorted to cloning. Furthermore, Huang and colleagues employed a CRISPR variant called base editor changing a single DNA letter without even cutting the double helix. The news is circulating among experts but has not yet attracted the media spotlight. Stem cell specialist Alessandro Bertero has brought it to the attention of CRISPeR Frenzy. According to the researcher involved in the British experiment just published in Nature, the latest paper from China is far from perfect but it’s quite interesting anyway (see his technical comment below). Continue reading

Editing embryos, the British way

embrioni UK.docxThey are the first human embryos edited in Europe and reported in scientific literature. The key difference with experiments already carried out in China and US is that the research published by Nature last week doesn’t have embryonic gene therapy in view. The London Francis Crick’s Institute team, in fact, was not interested in correcting disease-causing mutations but in increasing knowledge on human embryonic development. We asked one of the authors, Alessandro Bertero, to explain goals and results. The Italian researcher was pursuing his Ph.D. at Cambridge when he helped to refine the technique used by Kathy Niakan and colleagues to edit the genome of embryos. He answered our questions via Skype from America, where he continues working on embryonic stem cells as a postdoctoral fellow at Washington University Continue reading