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Biallelic variants in DNA2 cause microcephalic primordial dwarfism.
Tarnauskaite, Zygimante; 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; Jackson, Andrew P; Murina, Olga; Reijns, Martin A M.
Afiliação
  • Tarnauskaite Z; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Bicknell LS; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Marsh JA; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Murray JE; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Parry DA; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Logan CV; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Bober MB; Division of Genetics, Department of Pediatrics, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware.
  • de Silva DC; Department of Physiology, Faculty of Medicine, University of Kelaniya, Colombo, Sri Lanka.
  • Duker AL; Division of Genetics, Department of Pediatrics, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware.
  • Sillence D; Discipline of Genomic Medicine, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
  • Wise C; Western Sydney Genetics Program, Sydney Children's Hospitals Network, Westmead, Australia.
  • Jackson AP; Sarah M. and Charles E. Seay Center for Musculoskeletal Research, Texas Scottish, Rite Hospital for Children, Dallas, Texas.
  • Murina O; McDermott Center for Human Growth and Development, University of Texas, Southwestern Medical Center, Dallas, Texas.
  • Reijns MAM; Department of Orthopaedic Surgery, University of Texas Southwestern Medical Center, Dallas, Texas.
Hum Mutat ; 40(8): 1063-1070, 2019 08.
Article em En | MEDLINE | ID: mdl-31045292
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.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Variação Genética / DNA Helicases / Nanismo / Microcefalia Tipo de estudo: Prognostic_studies Limite: Adolescent / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Variação Genética / DNA Helicases / Nanismo / Microcefalia Tipo de estudo: Prognostic_studies Limite: Adolescent / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido