Reprogramming of the epigenome in neurodevelopmental disorders.
Ontology highlight
ABSTRACT: The etiology of neurodevelopmental disorders (NDDs) remains a challenge for researchers. Human brain development is tightly regulated and sensitive to cellular alterations caused by endogenous or exogenous factors. Intriguingly, the surge of clinical sequencing studies has revealed that many of these disorders are monogenic and monoallelic. Notably, chromatin regulation has emerged as highly dysregulated in NDDs, with many syndromes demonstrating phenotypic overlap, such as intellectual disabilities, with one another. Here we discuss epigenetic writers, erasers, readers, remodelers, and even histones mutated in NDD patients, predicted to affect gene regulation. Moreover, this review focuses on disorders associated with mutations in enzymes involved in histone acetylation and methylation, a
SUBMITTER: Wilson KD
PROVIDER: S-EPMC9462920 | biostudies-literature | 2022 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA