Article
Transient expression of an adenine base editor corrects the Hutchinson-Gilford progeria syndrome mutation and improves the skin phenotype in mice.
Nature communications - 2 Jun 2022
Whisenant Daniel, Lim Kayeong, Revêchon Gwladys, Yao Haidong, Bergo Martin O, Machtel Piotr, Kim Jin-Soo, Eriksson Maria
Abstract excerpt
Hutchinson-Gilford progeria syndrome (HGPS) is a rare premature ageing disorder caused by a point mutation in the LMNA gene (LMNA c.1824 C > T), resulting in the production of a detrimental protein called progerin. Adenine base editors recently emerged with a promising potential for HGPS gene therapy. However adeno-associated viral vector systems currently used in gene editing raise concerns, and the long-term...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
