PUBLICATION

Pathway specific effects of ADSL deficiency on neurodevelopment

Authors
Dutto, I., Gerhards, J., Herrera, A., Souckova, O., ?kopová, V., Smak, J., Junza, A., Yanes, O., Boeckx, C., Burkhalter, M.D., Zikánová, M., Pons, S., Philipp, M., Lüders, J., Stracker, T.H.
ID
ZDB-PUB-220209-9
Date
2022
Source
eLIFE   11: (Journal)
Registered Authors
Philipp, Melanie
Keywords
cell biology, chicken, developmental biology, human, zebrafish
MeSH Terms
  • Autistic Disorder/metabolism*
  • Humans
  • Purine-Pyrimidine Metabolism, Inborn Errors/metabolism*
  • Zebrafish/metabolism
  • Adenylosuccinate Lyase/deficiency*
  • Adenylosuccinate Lyase/metabolism*
  • Neurogenesis*
  • Microcephaly/metabolism
  • Ribonucleotides/metabolism
  • Purines/metabolism
  • Autism Spectrum Disorder/metabolism
  • Cell Cycle
  • Chickens/metabolism
  • Phenotype
  • Aminoimidazole Carboxamide/analogs & derivatives
  • Aminoimidazole Carboxamide/metabolism
  • Cell Line
  • Cell Cycle Proteins/metabolism
  • Microtubule-Associated Proteins/metabolism
  • Phosphoproteins/metabolism
  • Ciliopathies/metabolism
  • DNA Damage
  • Animals
(all 23)
PubMed
35133277 Full text @ Elife
Abstract
Adenylosuccinate Lyase (ADSL) functions in de novo purine biosynthesis (DNPS) and the purine nucleotide cycle. ADSL deficiency (ADSLD) causes numerous neurodevelopmental pathologies, including microcephaly and autism spectrum disorder. ADSLD patients have normal serum purine nucleotide levels but exhibit accumulation of dephosphorylated ADSL substrates, S-Ado and SAICAr, the latter being implicated in neurotoxic effects through unknown mechanisms. We examined the phenotypic effects of ADSL depletion in human cells and their relation to phenotypic outcomes. Using specific interventions to compensate for reduced purine levels or modulate SAICAr accumulation, we found that diminished AMP levels resulted in increased DNA damage signaling and cell cycle delays, while primary ciliogenesis was impaired specifically by loss of ADSL or administration of SAICAr. ADSL deficient chicken and zebrafish embryos displayed impaired neurogenesis and microcephaly. Neuroprogenitor attrition in zebrafish embryos was rescued by pharmacological inhibition of DNPS, but not increased nucleotide concentration. Zebrafish also displayed phenotypes commonly linked to ciliopathies. Our results suggest that both reduced purine levels and impaired DNPS contribute to neurodevelopmental pathology in ADSLD and that defective ciliogenesis may influence the ADSLD phenotypic spectrum.
Genes / Markers
Figures
Figure Gallery (8 images)
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Expression
Gene Antibody Fish Conditions Stage Qualifier Anatomy Assay Figure
spawAB/EKW + MO1-adslstandard conditions20-25 somitesISH
1 - 1 of 1
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Phenotype
Mutations / Transgenics
No data available
Human Disease / Model
Human Disease Fish Conditions Evidence
purine-pyrimidine metabolic disorderTAS
1 - 1 of 1
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Sequence Targeting Reagents
Target Reagent Reagent Type
adslMO1-adslMRPHLNO
adslMO2-adslMRPHLNO
1 - 2 of 2
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Fish
1 - 1 of 1
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Antibodies
Orthology
Gene Orthology
adsl
1 - 1 of 1
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Engineered Foreign Genes
No data available
Mapping
No data available