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Genetic architecture of band neutrophil fraction in Iceland.
Oskarsson, Gudjon R; Magnusson, Magnus K; Oddsson, Asmundur; Jensson, Brynjar O; Fridriksdottir, Run; Arnadottir, Gudny A; Katrinardottir, Hildigunnur; Rognvaldsson, Solvi; Halldorsson, Gisli H; Sveinbjornsson, Gardar; Ivarsdottir, Erna V; Stefansdottir, Lilja; Ferkingstad, Egil; Norland, Kristjan; Tragante, Vinicius; Saemundsdottir, Jona; Jonasdottir, Aslaug; Jonasdottir, Adalbjorg; Sigurjonsdottir, Svanhvit; Petursdottir, Karen O; Davidsson, Olafur B; Rafnar, Thorunn; Holm, Hilma; Olafsson, Isleifur; Onundarson, Pall T; Vidarsson, Brynjar; Sigurdardottir, Olof; Masson, Gisli; Gudbjartsson, Daniel F; Jonsdottir, Ingileif; Norddahl, Gudmundur L; Thorsteinsdottir, Unnur; Sulem, Patrick; Stefansson, Kari.
Afiliação
  • Oskarsson GR; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Magnusson MK; Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.
  • Oddsson A; deCODE genetics/Amgen Inc., Reykjavik, Iceland. magnus.magnusson@decode.is.
  • Jensson BO; Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland. magnus.magnusson@decode.is.
  • Fridriksdottir R; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Arnadottir GA; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Katrinardottir H; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Rognvaldsson S; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Halldorsson GH; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Sveinbjornsson G; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Ivarsdottir EV; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Stefansdottir L; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Ferkingstad E; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Norland K; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Tragante V; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Saemundsdottir J; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Jonasdottir A; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Jonasdottir A; Department of Cardiology, Division Heart and Lungs, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
  • Sigurjonsdottir S; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Petursdottir KO; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Davidsson OB; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Rafnar T; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Holm H; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Olafsson I; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Onundarson PT; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Vidarsson B; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Sigurdardottir O; Department of Clinical Biochemistry, Landspitali, The National University Hospital of Iceland, Reykjavik, Iceland.
  • Masson G; Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland.
  • Gudbjartsson DF; Department of Laboratory Hematology, Landspitali, The National University Hospital of Iceland, Reykjavik, Iceland.
  • Jonsdottir I; Department of Laboratory Hematology, Landspitali, The National University Hospital of Iceland, Reykjavik, Iceland.
  • Norddahl GL; The Laboratory in Mjodd, RAM, Reykjavik, Iceland.
  • Thorsteinsdottir U; Department of Clinical Biochemistry, Akureyri Hospital, Akureyri, Iceland.
  • Sulem P; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
  • Stefansson K; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
Commun Biol ; 5(1): 525, 2022 06 01.
Article em En | MEDLINE | ID: mdl-35650273
ABSTRACT
The characteristic lobulated nuclear morphology of granulocytes is partially determined by composition of nuclear envelope proteins. Abnormal nuclear morphology is primarily observed as an increased number of hypolobulated immature neutrophils, called band cells, during infection or in rare envelopathies like Pelger-Huët anomaly. To search for sequence variants affecting nuclear morphology of granulocytes, we performed a genome-wide association study using band neutrophil fraction from 88,101 Icelanders. We describe 13 sequence variants affecting band neutrophil fraction at nine loci. Five of the variants are at the Lamin B receptor (LBR) locus, encoding an inner nuclear membrane protein. Mutations in LBR are linked to Pelger-Huët anomaly. In addition, we identify cosegregation of a rare stop-gain sequence variant in LBR and Pelger Huët anomaly in an Icelandic eight generation pedigree, initially reported in 1963. Two of the other loci include genes which, like LBR, play a role in the nuclear membrane function and integrity. These GWAS results highlight the role proteins of the inner nuclear membrane have as important for neutrophil nuclear morphology.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anomalia de Pelger-Huët Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anomalia de Pelger-Huët Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2022 Tipo de documento: Article