De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy

Am J Hum Genet. 2020 May 7;106(5):717-725. doi: 10.1016/j.ajhg.2020.04.001. Epub 2020 Apr 23.


We identified three unrelated individuals with de novo missense variants in CDK19, encoding a cyclin-dependent kinase protein family member that predominantly regulates gene transcription. These individuals presented with hypotonia, global developmental delay, epileptic encephalopathy, and dysmorphic features. CDK19 is conserved between vertebrate and invertebrate model organisms, but currently abnormalities in CDK19 are not known to be associated with a human disorder. Loss of Cdk8, the fly homolog of CDK19, causes larval lethality, which is suppressed by expression of human CDK19 reference cDNA. In contrast, the CDK19 p.Tyr32His and p.Thr196Ala variants identified in the affected individuals fail to rescue the loss of Cdk8 and behave as null alleles. Additionally, neuronal RNAi-mediated knockdown of Cdk8 in flies results in semi-lethality. The few eclosing flies exhibit severe seizures and a reduced lifespan. Both phenotypes are fully suppressed by moderate expression of the CDK19 reference cDNA but not by expression of the two variants. Finally, loss of Cdk8 causes an obvious loss of boutons and synapses at larval neuromuscular junctions (NMJs). Together, our findings demonstrate that human CDK19 fully replaces the function of Cdk8 in the fly, the human disease-associated CDK19 variants behave as strong loss-of-function variants, and deleterious CDK19 variants underlie a syndromic neurodevelopmental disorder.

Keywords: Cdk8; Drosophila; West syndrome; bang sensitivity; de novo; dominant variants; genetic disease; infantile spasms; rare disease; seizure.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Animals
  • Brain Diseases / genetics*
  • Child, Preschool
  • Cyclin-Dependent Kinase 8 / deficiency
  • Cyclin-Dependent Kinase 8 / genetics
  • Cyclin-Dependent Kinases / genetics*
  • Drosophila Proteins / deficiency
  • Drosophila Proteins / genetics
  • Drosophila melanogaster / genetics
  • Epilepsy, Generalized / genetics*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Intellectual Disability / genetics*
  • Male
  • Mutation, Missense / genetics*
  • Neuromuscular Junction
  • Rare Diseases / genetics
  • Seizures / genetics
  • Syndrome
  • Young Adult


  • Drosophila Proteins
  • CDK19 protein, human
  • Cdk8 protein, Drosophila
  • Cyclin-Dependent Kinase 8
  • Cyclin-Dependent Kinases