PUBLICATION

Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

Authors
Kohler, J.N., Legro, N.R., Baldridge, D., Shin, J., Bowman, A., Ugur, B., Jackstadt, M.M., Shriver, L.P., Patti, G.J., Zhang, B., Feng, W., McAdow, A.R., Goddard, P., Ungar, R.A., Jensen, T., Smith, K.S., Fresard, L., Alvarez, R., Bonner, D., Reuter, C.M., McCormack, C., Kravets, E., Marwaha, S., Holt, J.M., Undiagnosed Diseases Network, Worthey, E., Ashley, E.A., Montgomery, S.B., Fisher, P., Postlethwait, J., De Camilli, P., Solnica-Krezel, L., Bernstein, J.A., Wheeler, M.T.
ID
ZDB-PUB-240520-9
Date
2024
Source
Genetics in medicine : official journal of the American College of Medical Genetics   26(9): 101166 (Journal)
Registered Authors
Postlethwait, John H., Shin, Jimann, Solnica-Krezel, Lilianna
Keywords
FAM177A1, developmental delay, inflammation, intellectual disability, macrocephaly, neurodevelopment, zebrafish
MeSH Terms
  • Golgi Apparatus*/genetics
  • Golgi Apparatus*/metabolism
  • Loss of Function Mutation*
  • Child
  • Membrane Proteins/genetics
  • Membrane Proteins/metabolism
  • Humans
  • Male
  • Child, Preschool
  • Zebrafish*/genetics
  • Neurodevelopmental Disorders*/genetics
  • Neurodevelopmental Disorders*/metabolism
  • Neurodevelopmental Disorders*/pathology
  • Female
  • Phenotype
  • Animals
  • Pedigree
  • Intellectual Disability/genetics
  • Intellectual Disability/metabolism
  • Intellectual Disability/pathology
PubMed
38767059 Full text @ Genet. Med.
Abstract
The function of FAM177A1 and its relationship to human disease is largely unknown. Recent studies have demonstrated FAM177A1 to be a critical immune-associated gene. One previous case study has linked FAM177A1 to a neurodevelopmental disorder in four siblings.
We identified five individuals from three unrelated families with biallelic variants in FAM177A1. The physiological function of FAM177A1 was studied in a zebrafish model organism and human cell lines with loss-of-function variants similar to the affected cohort.
These individuals share a characteristic phenotype defined by macrocephaly, global developmental delay, intellectual disability, seizures, behavioral abnormalities, hypotonia, and gait disturbance. We show that FAM177A1 localizes to the Golgi complex in mammalian and zebrafish cells. Intersection of the RNA-seq and metabolomic datasets from FAM177A1-deficient human fibroblasts and whole zebrafish larvae demonstrated dysregulation of pathways associated with apoptosis, inflammation, and negative regulation of cell proliferation.
Our data sheds light on the emerging function of FAM177A1 and defines FAM177A1-related neurodevelopmental disorder as a new clinical entity.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping