PRIM1 deficiency causes a distinctive primordial dwarfism syndrome

Genes Dev. 2020 Nov 1;34(21-22):1520-1533. doi: 10.1101/gad.340190.120. Epub 2020 Oct 15.

Abstract

DNA replication is fundamental for cell proliferation in all organisms. Nonetheless, components of the replisome have been implicated in human disease, and here we report PRIM1 encoding the catalytic subunit of DNA primase as a novel disease gene. Using a variant classification agnostic approach, biallelic mutations in PRIM1 were identified in five individuals. PRIM1 protein levels were markedly reduced in patient cells, accompanied by replication fork asymmetry, increased interorigin distances, replication stress, and prolonged S-phase duration. Consequently, cell proliferation was markedly impaired, explaining the patients' extreme growth failure. Notably, phenotypic features distinct from those previously reported with DNA polymerase genes were evident, highlighting differing developmental requirements for this core replisome component that warrant future investigation.

Keywords: DNA replication; genome stability; growth disorders; human genetics; rare disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Primase / chemistry
  • DNA Primase / deficiency
  • DNA Primase / genetics*
  • Dwarfism / diagnostic imaging
  • Dwarfism / genetics*
  • Dwarfism / pathology
  • Female
  • Fetal Growth Retardation / diagnostic imaging
  • Fetal Growth Retardation / genetics*
  • Fetal Growth Retardation / pathology
  • Genetic Variation
  • Humans
  • Infant
  • Male
  • Pedigree
  • Syndrome

Substances

  • DNA Primase
  • PRIM1 protein, human