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http://purl.uniprot.org/citations/31174490http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31174490http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31174490http://www.w3.org/2000/01/rdf-schema#comment"

Background

N-terminal acetylation is a common protein modification in human cells and is catalysed by N-terminal acetyltransferases (NATs), mostly cotranslationally. The NAA10-NAA15 (NatA) protein complex is the major NAT, responsible for acetylating ~ 40% of human proteins. Recently, NAA10 germline variants were found in patients with the X-linked lethal Ogden syndrome, and in other familial or de novo cases with variable degrees of developmental delay, intellectual disability (ID) and cardiac anomalies.

Methods

Here we report a novel NAA10 (NM_003491.3) c.248G > A, p.(R83H) missense variant in NAA10 which was detected by whole exome sequencing in two unrelated boys with intellectual disability, developmental delay, ADHD like behaviour, very limited speech and cardiac abnormalities. We employ in vitro acetylation assays to functionally test the impact of this variant on NAA10 enzyme activity.

Results

Functional characterization of NAA10-R83H by in vitro acetylation assays revealed a reduced enzymatic activity of monomeric NAA10-R83H. This variant is modelled to have an altered charge density in the acetyl-coenzyme A (Ac-CoA) binding region of NAA10.

Conclusions

We show that NAA10-R83H has a reduced monomeric catalytic activity, likely due to impaired enzyme-Ac-CoA binding. Our data support a model where reduced NAA10 and/or NatA activity cause the phenotypes observed in the two patients."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.org/dc/terms/identifier"doi:10.1186/s12881-019-0803-1"xsd:string
http://purl.uniprot.org/citations/31174490http://purl.org/dc/terms/identifier"doi:10.1186/s12881-019-0803-1"xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Arnesen T."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Arnesen T."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Lynch S.A."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Lynch S.A."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Soerensen K.P."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Soerensen K.P."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Toerring P.M."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Toerring P.M."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Damkjaer M."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Damkjaer M."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Geithus A.S."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Geithus A.S."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Ree R."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/author"Ree R."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/name"BMC Med. Genet."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/name"BMC Med. Genet."xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/pages"101"xsd:string
http://purl.uniprot.org/citations/31174490http://purl.uniprot.org/core/pages"101"xsd:string
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