341 Repeats Is Not Enough for Methylation in a New Fragile X Mouse Model.
Ontology highlight
ABSTRACT: Fragile X syndrome (FXS) is a leading monogenic cause of intellectual disability and autism spectrum disorders, spurring decades of intense research and a multitude of mouse models. So far, these models do not recapitulate the genetic underpinning of classical FXS-CGG repeat-induced methylation of the Fmr1 locus-and their findings have failed to translate into the clinic. We sought to answer whether this disparity was because of low repeat length and generated a novel mouse line with 341 repeats, Fmr1hs341 , which is the largest allele in mice reported to date. This repeat length is significantly longer than the 200 repeats generally required for methylation of the repeat tract and promoter region in FXS patients, which leads to silencing of the FMR1 gene. B
SUBMITTER: Colvin S
PROVIDER: S-EPMC9469916 | biostudies-literature | 2022 Sep-Oct
REPOSITORIES: biostudies-literature
ACCESS DATA