Ontology highlight
ABSTRACT:
SUBMITTER: Frankel D
PROVIDER: S-EPMC8800101 | biostudies-literature | 2022 Feb
REPOSITORIES: biostudies-literature
Frankel Diane D Delecourt Valérie V Novoa-Del-Toro Elva-María EM Robin Jérôme D JD Airault Coraline C Bartoli Catherine C Carabalona Aurélie A Perrin Sophie S Mazaleyrat Kilian K De Sandre-Giovannoli Annachiara A Magdinier Frederique F Baudot Anaïs A Lévy Nicolas N Kaspi Elise E Roll Patrice P
iScience 20220110 2
Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disorder, in which an abnormal and toxic protein called progerin, accumulates in cell nuclei, leading to major cellular defects. Among them, chromatin remodeling drives gene expression changes, including miRNA dysregulation. In our study, we evaluated miRNA expression profiles in HGPS and control fibroblasts. We identified an enrichment of overexpressed miRNAs belonging to the 14q32.2-14q32.3 miRNA cluster. Using 3D FISH, we demonstra ...[more]