CDK19-related disorder results from both loss-of-function and gain-of-function de novo missense variants.
Genet Med
; 23(6): 1050-1057, 2021 06.
Article
in En
| MEDLINE
| ID: mdl-33495529
ABSTRACT
PURPOSE:
To expand the recent description of a new neurodevelopmental syndrome related to alterations in CDK19.METHODS:
Individuals were identified through international collaboration. Functional studies included autophosphorylation assays for CDK19 Gly28Arg and Tyr32His variants and in vivo zebrafish assays of the CDK19G28R and CDK19Y32H.RESULTS:
We describe 11 unrelated individuals (age range 9 months to 14 years) with de novo missense variants mapped to the kinase domain of CDK19, including two recurrent changes at residues Tyr32 and Gly28. In vitro autophosphorylation and substrate phosphorylation assays revealed that kinase activity of protein was lower for p.Gly28Arg and higher for p.Tyr32His substitutions compared with that of the wild-type protein. Injection of CDK19 messenger RNA (mRNA) with either the Tyr32His or the Gly28Arg variants using in vivo zebrafish model significantly increased fraction of embryos with morphological abnormalities. Overall, the phenotype of the now 14 individuals with CDK19-related disorder includes universal developmental delay and facial dysmorphism, hypotonia (79%), seizures (64%), ophthalmologic anomalies (64%), and autism/autistic traits (56%).CONCLUSION:
CDK19 de novo missense variants are responsible for a novel neurodevelopmental disorder. Both kinase assay and zebrafish experiments showed that the pathogenetic mechanism may be more diverse than previously thought.
Full text:
1
Database:
MEDLINE
Main subject:
Neurodevelopmental Disorders
/
Intellectual Disability
Limits:
Animals
/
Humans
/
Infant
Language:
En
Journal:
Genet Med
Journal subject:
GENETICA MEDICA
Year:
2021
Type:
Article
Affiliation country:
United States