Biallelic variants in DNA2 cause microcephalic primordial dwarfism

Žygimantė Tarnauskaitė, Louise S. Bicknell, Joseph A. Marsh, Jennie E. Murray, David A. Parry, Clare V. Logan, Michael B. Bober, Deepthi C. de Silva, Angela L. Duker, David Sillence, Carol A Wise, Andrew P. Jackson, Olga Murina, Martin A.M. Reijns

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Microcephalic primordial dwarfism (MPD) is a group of rare single-gene disorders characterized by the extreme reduction in brain and body size from early development onwards. Proteins encoded by MPD-associated genes play important roles in fundamental cellular processes, notably genome replication and repair. Here we report the identification of four MPD individuals with biallelic variants in DNA2, which encodes an adenosine triphosphate (ATP)-dependent helicase/nuclease involved in DNA replication and repair. We demonstrate that the two intronic variants (c.1764-38_1764-37ins(53) and c.74+4A>C) found in these individuals substantially impair DNA2 transcript splicing. Additionally, we identify a missense variant (c.1963A>G), affecting a residue of the ATP-dependent helicase domain that is highly conserved between humans and yeast, with the resulting substitution (p.Thr655Ala) predicted to directly impact ATP/ADP (adenosine diphosphate) binding by DNA2. Our findings support the pathogenicity of these variants as biallelic hypomorphic mutations, establishing DNA2 as an MPD disease gene.

Original languageEnglish (US)
Pages (from-to)1063-1070
Number of pages8
JournalHuman Mutation
Volume40
Issue number8
DOIs
StatePublished - Jan 1 2019

Fingerprint

Dwarfism
Adenosine Triphosphate
Adenosine Diphosphate
Genes
Body Size
DNA Replication
DNA Repair
Virulence
Yeasts
Genome
Mutation
Brain
Proteins

Keywords

  • DNA repair
  • DNA replication
  • DNA2
  • growth
  • microcephalic primordial dwarfism

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Tarnauskaitė, Ž., Bicknell, L. S., Marsh, J. A., Murray, J. E., Parry, D. A., Logan, C. V., ... Reijns, M. A. M. (2019). Biallelic variants in DNA2 cause microcephalic primordial dwarfism. Human Mutation, 40(8), 1063-1070. https://doi.org/10.1002/humu.23776

Biallelic variants in DNA2 cause microcephalic primordial dwarfism. / Tarnauskaitė, Žygimantė; Bicknell, Louise S.; Marsh, Joseph A.; Murray, Jennie E.; Parry, David A.; Logan, Clare V.; Bober, Michael B.; de Silva, Deepthi C.; Duker, Angela L.; Sillence, David; Wise, Carol A; Jackson, Andrew P.; Murina, Olga; Reijns, Martin A.M.

In: Human Mutation, Vol. 40, No. 8, 01.01.2019, p. 1063-1070.

Research output: Contribution to journalArticle

Tarnauskaitė, Ž, Bicknell, LS, Marsh, JA, Murray, JE, Parry, DA, Logan, CV, Bober, MB, de Silva, DC, Duker, AL, Sillence, D, Wise, CA, Jackson, AP, Murina, O & Reijns, MAM 2019, 'Biallelic variants in DNA2 cause microcephalic primordial dwarfism', Human Mutation, vol. 40, no. 8, pp. 1063-1070. https://doi.org/10.1002/humu.23776
Tarnauskaitė Ž, Bicknell LS, Marsh JA, Murray JE, Parry DA, Logan CV et al. Biallelic variants in DNA2 cause microcephalic primordial dwarfism. Human Mutation. 2019 Jan 1;40(8):1063-1070. https://doi.org/10.1002/humu.23776
Tarnauskaitė, Žygimantė ; Bicknell, Louise S. ; Marsh, Joseph A. ; Murray, Jennie E. ; Parry, David A. ; Logan, Clare V. ; Bober, Michael B. ; de Silva, Deepthi C. ; Duker, Angela L. ; Sillence, David ; Wise, Carol A ; Jackson, Andrew P. ; Murina, Olga ; Reijns, Martin A.M. / Biallelic variants in DNA2 cause microcephalic primordial dwarfism. In: Human Mutation. 2019 ; Vol. 40, No. 8. pp. 1063-1070.
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