Loss of Ten1 in Mice Induces Telomere Shortening and Models Human Dyskeratosis Congenita

    April 2025 in “ Science Advances
    Adrián Sanz‐Moreno, Lore Becker, Kan Xie, Patricia da Silva‐Buttkus, Nathalia Romanelli Vicente Dragano, Juan Antonio Aguilar‐Pimentel, Oana V. Amarie, Julia Calzada‐Wack, Markus Kraiger, Stefanie Leuchtenberger, Claudia Seisenberger, Susan Marschall, Birgit Rathkolb, Enzo Scifo, Ting Liu, Anoja Thanabalasingam, Raúl Sánchez-Vazquez, Paula Felippe Martinez, Marı́a A. Blasco, Sharon A. Savage, Helmut Fuchs, Dan Ehninger, Valérie Gailus‐Durner, Martin Hrabě de Angelis
    Studysummary This study found that mice with a homozygous knockout of the Ten1 gene, developed through CRISPR-Cas9-mediated exon 3 deletion, exhibited telomere shortening and symptoms consistent with accelerated aging, such as reduced lifespan, skin changes, aplastic anemia, and cerebellar hypoplasia.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
    Discuss this study in the Community →

    Research cited in this study

    2 / 2 results