The role of DEAD- and DExH-box RNA helicases in neurodevelopmental disorders.

P-bodies R-loop miRNA stress granules translation

Journal

Frontiers in molecular neuroscience
ISSN: 1662-5099
Titre abrégé: Front Mol Neurosci
Pays: Switzerland
ID NLM: 101477914

Informations de publication

Date de publication:
2024
Historique:
received: 09 04 2024
accepted: 22 07 2024
medline: 16 8 2024
pubmed: 16 8 2024
entrez: 16 8 2024
Statut: epublish

Résumé

Neurodevelopmental disorders (NDDs) represent a large group of disorders with an onset in the neonatal or early childhood period; NDDs include intellectual disability (ID), autism spectrum disorders (ASD), attention deficit hyperactivity disorders (ADHD), seizures, various motor disabilities and abnormal muscle tone. Among the many underlying Mendelian genetic causes for these conditions, genes coding for proteins involved in all aspects of the gene expression pathway, ranging from transcription, splicing, translation to the eventual RNA decay, feature rather prominently. Here we focus on two large families of RNA helicases (DEAD- and DExH-box helicases). Genetic variants in the coding genes for several helicases have recently been shown to be associated with NDD. We address genetic constraints for helicases, types of pathological variants which have been discovered and discuss the biological pathways in which the affected helicase proteins are involved.

Identifiants

pubmed: 39149612
doi: 10.3389/fnmol.2024.1414949
pmc: PMC11324592
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1414949

Informations de copyright

Copyright © 2024 Lederbauer, Das, Piton, Lessel and Kreienkamp.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Johannes Lederbauer (J)

Institute of Human Genetics, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Sarada Das (S)

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Amelie Piton (A)

Department of Translational Medicine and Neurogenetics, Institute of Genetics and Molecular and Cellular Biology, Strasbourg University, CNRS UMR7104, INSERM U1258, Illkirch, France.

Davor Lessel (D)

Institute of Human Genetics, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Hans-Jürgen Kreienkamp (HJ)

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Classifications MeSH