PUBLICATION

Association of HECW2 variants with developmental and epileptic encephalopathy and knockdown of zebrafish hecw2a

Authors
Lu, Q., Zhang, M.N., Shi, X.Y., Zhang, L.Q., Wang, Y.Y., Liu, L.Y., He, W., Chen, H.M., He, B., Zou, L.P.
ID
ZDB-PUB-201120-157
Date
2020
Source
American journal of medical genetics. Part A   185(2): 377-383 (Journal)
Registered Authors
He, Bing
Keywords
HECW2, developmental encephalopathy, epilepsy, zebrafish model
MeSH Terms
  • Adolescent
  • Animals
  • Brain Diseases/epidemiology
  • Brain Diseases/genetics*
  • Brain Diseases/pathology
  • Child
  • Child, Preschool
  • Disease Models, Animal
  • Exome Sequencing
  • Genetic Predisposition to Disease
  • Humans
  • Infant
  • Intellectual Disability/epidemiology
  • Intellectual Disability/genetics*
  • Intellectual Disability/pathology
  • Male
  • Mutation/genetics
  • Ubiquitin-Protein Ligases/genetics*
  • Zebrafish/genetics
  • Zebrafish Proteins/genetics*
PubMed
33205896 Full text @ Am. J. Med. Genet. A
Abstract
Developmental and epileptic encephalopathy (DEE) is a severe encephalopathy in infants and early childhood. In this study we reported a recurrent de novo variant (c.3985C>T, p.R1330W) in HECW2 (HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2) (MIM# 617245) identified by screening 240 patients with DEE and summarized clinical features of published DEE patients with HECW2 variants. Functionally, transcriptional knockdown of zebrafish hecw2a led to early morphological abnormalities in the brain tissues. These results suggest a potential functional link between HECW2 dysfunction and brain development.
Genes / Markers
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping