Transposable elements are mobile genetic elements that can relocate within the genome and disrupt the normal function of genes, but are at the same time a source of evolutionary diversity. The lab of Tugce Aktas at the Max Planck Institute for Molecular Genetics has identified a novel pathway that keeps the activity of transposons in somatic cells in check after they have been transcribed. Their findings have now been published in Nature. The work is a collaboration with the labs of Zachary D. Smith (Yale Stem Cell Center, USA) and Franz-Josef Müller (Universitätsklinikum Schleswig-Holstein, Germany)