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1000 Titel
  • Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain
1000 Autor/in
  1. Neuser, Sonja |
  2. krey, ilona |
  3. Schwan, Annemarie |
  4. Abou Jamra, Rami |
  5. Bartolomaeus, Tobias |
  6. Döring, Jan |
  7. Syrbe, Steffen |
  8. Plassmann, Margit |
  9. Rohde, Stefan |
  10. Roth, Christian |
  11. Rehder, Helga |
  12. Radtke, Maximilian |
  13. Le Duc, Diana |
  14. Schubert, Susanna |
  15. Bermudez-Guzman, Luis |
  16. Leal, Alejandro |
  17. Schoner, Katharina |
  18. Popp, Bernt |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-10-25
1000 Erschienen in
1000 Quellenangabe
  • 30(1):101-110
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1038/s41431-021-00982-y |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738728/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Biallelic PNKP variants cause heterogeneous disorders ranging from neurodevelopmental disorder with microcephaly/seizures to adult-onset Charcot-Marie-Tooth disease. To date, only postnatal descriptions exist. We present the first prenatal diagnosis of PNKP-related primary microcephaly. Pathological examination of a male fetus in the 18th gestational week revealed micrencephaly with extracerebral malformations and thus presumed syndromic microcephaly. A recessive disorder was suspected because of previous pregnancy termination for similar abnormalities. Prenatal trio-exome sequencing identified compound heterozygosity for the PNKP variants c.498G>A, p.[(=),0?] and c.302C>T, p.(Pro101Leu). Segregation confirmed both variants in the sister fetus. Through RNA analyses, we characterized exon 4 skipping affecting the PNKP forkhead-associated (FHA) and phosphatase domains (p.Leu67_Lys166del) as the predominant effect of the paternal c.498G>A variant. We retrospectively investigated two unrelated individuals diagnosed with biallelic PNKP-variants to compare prenatal/postnatal phenotypes. Both carry the splice donor variant c.1029+2T>C in trans with a variant in the FHA domain (c.311T>C, p.(Leu104Pro); c.151G>C, p.(Val51Leu)). RNA-seq showed complex splicing for c.1029+2T>C and c.151G>C. Structural modeling revealed significant clustering of missense variants in the FHA domain with variants generating structural damage. Our clinical description extends the PNKP-continuum to the prenatal stage. Investigating possible PNKP-variant effects using RNA and structural modeling, we highlight the mutational complexity and exemplify a PNKP-variant characterization framework.
1000 Sacherschließung
lokal Female [MeSH]
lokal Prenatal Diagnosis [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal DNA Repair Enzymes/genetics [MeSH]
lokal Protein Domains [MeSH]
lokal Paediatric neurological disorders
lokal Phosphotransferases (Alcohol Group Acceptor)/genetics [MeSH]
lokal Mutation, Missense [MeSH]
lokal Genetics research
lokal DNA Repair Enzymes/chemistry [MeSH]
lokal Article
lokal RNA Splicing [MeSH]
lokal Male [MeSH]
lokal Microcephaly/diagnosis [MeSH]
lokal Microcephaly/genetics [MeSH]
lokal Phosphotransferases (Alcohol Group Acceptor)/chemistry [MeSH]
lokal Phenotype [MeSH]
lokal RNA splicing
lokal Genetic testing
lokal Fetus/abnormalities [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-2875-8791|https://orcid.org/0000-0002-9168-7615|https://frl.publisso.de/adhoc/uri/U2Nod2FuLCBBbm5lbWFyaWU=|https://orcid.org/0000-0002-1542-1399|https://orcid.org/0000-0002-5406-0776|https://frl.publisso.de/adhoc/uri/RMO2cmluZywgSmFu|https://frl.publisso.de/adhoc/uri/U3lyYmUsIFN0ZWZmZW4=|https://frl.publisso.de/adhoc/uri/UGxhc3NtYW5uLCBNYXJnaXQ=|https://frl.publisso.de/adhoc/uri/Um9oZGUsIFN0ZWZhbg==|https://frl.publisso.de/adhoc/uri/Um90aCwgQ2hyaXN0aWFu|https://frl.publisso.de/adhoc/uri/UmVoZGVyLCBIZWxnYQ==|https://frl.publisso.de/adhoc/uri/UmFkdGtlLCBNYXhpbWlsaWFu|https://frl.publisso.de/adhoc/uri/TGUgRHVjLCBEaWFuYQ==|https://frl.publisso.de/adhoc/uri/U2NodWJlcnQsIFN1c2FubmE=|https://orcid.org/0000-0002-0749-4010|https://orcid.org/0000-0002-5384-8166|https://frl.publisso.de/adhoc/uri/U2Nob25lciwgS2F0aGFyaW5h|https://orcid.org/0000-0002-3679-1081
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