PUBLICATION

DTYMK is essential for genome integrity and neuronal survival

Authors
Vanoevelen, J.M., Bierau, J., Grashorn, J.C., Lambrichs, E., Kamsteeg, E.J., Bok, L.A., Wevers, R.A., van der Knaap, M.S., Bugiani, M., Frisk, J.H., Colnaghi, R., O'Driscoll, M., Hellebrekers, D.M.E.I., Rodenburg, R., Ferreira, C.R., Brunner, H.G., van den Wijngaard, A., Abdel-Salam, G.M.H., Wang, L., Stumpel, C.T.R.M.
ID
ZDB-PUB-211221-7
Date
2021
Source
Acta Neuropathologica   143(2): 245-262 (Journal)
Registered Authors
Keywords
DTYMK, Genome instability, Nucleotide metabolism, Zebrafish, dTMPK
MeSH Terms
  • Animals
  • Female
  • Humans
  • Male
  • Microcephaly/genetics
  • Mutation
  • Neurodegenerative Diseases/genetics*
  • Nucleoside-Phosphate Kinase/genetics*
  • Zebrafish
PubMed
34918187 Full text @ Acta Neuropathol.
Abstract
Nucleotide metabolism is a complex pathway regulating crucial cellular processes such as nucleic acid synthesis, DNA repair and proliferation. This study shows that impairment of the biosynthesis of one of the building blocks of DNA, dTTP, causes a severe, early-onset neurodegenerative disease. Here, we describe two unrelated children with bi-allelic variants in DTYMK, encoding dTMPK, which catalyzes the penultimate step in dTTP biosynthesis. The affected children show severe microcephaly and growth retardation with minimal neurodevelopment. Brain imaging revealed severe cerebral atrophy and disappearance of the basal ganglia. In cells of affected individuals, dTMPK enzyme activity was minimal, along with impaired DNA replication. In addition, we generated dtymk mutant zebrafish that replicate this phenotype of microcephaly, neuronal cell death and early lethality. An increase of ribonucleotide incorporation in the genome as well as impaired responses to DNA damage were observed in dtymk mutant zebrafish, providing novel pathophysiological insights. It is highly remarkable that this deficiency is viable as an essential component for DNA cannot be generated, since the metabolic pathway for dTTP synthesis is completely blocked. In summary, by combining genetic and biochemical approaches in multiple models we identified loss-of-function of DTYMK as the cause of a severe postnatal neurodegenerative disease and highlight the essential nature of dTTP synthesis in the maintenance of genome stability and neuronal survival.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping