Molecular and structural characterization of a novel high-prevalence antigen of the Augustine blood group system.

blood group genomics equilibrative nucleoside transporter 1 hematology - red cells immunohematology

Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
03 2023
Historique:
revised: 19 12 2022
received: 11 10 2022
accepted: 27 12 2022
pubmed: 7 2 2023
medline: 23 3 2023
entrez: 6 2 2023
Statut: ppublish

Résumé

An antibody directed against a high-prevalence red blood cell (RBC) antigen was detected in a 67-year-old female patient of North African ancestry with a history of a single pregnancy and blood transfusion. So far, the specificity of the proband's alloantibody remained unknown in our immunohematology reference laboratory. Whole-exome sequencing (WES) was performed on the proband's DNA. The reactivity to the SLC29A1-encoded ENT1 adenosine transporter was investigated by flow cytometry analyses of ENT1-expressing HEK293 cells, and RBCs from Augustine-typed individuals. Erythrocyte protein expression level, nucleoside-binding capacity, and molecular structure of the proband's ENT1 variant were further explored by western blot, flow cytometry, and molecular dynamics calculations, respectively. A missense variant was identified in the SLC29A1 gene, which encodes the Augustine blood group system. It arises from homozygosity for a rare c.242A > G missense mutation that results in a nonsynonymous p.Asn81Ser substitution within the large extracellular loop of ENT1. Flow cytometry analyses demonstrated that the proband's antibody was reactive against HEK-293 cells transfected with control but not proband's SLC29A1 cDNA. Consistent with this finding, proband's antibody was found to be reactive with At(a-) (AUG:-2), but not AUG:-1 (null phenotype) RBCs. Data from structural analysis further supported that the proband's p.Asn81Ser variation does not alter ENT1 binding of its specific inhibitor NBMPR. Our study provides evidence for a novel high-prevalence antigen, AUG4 (also called ATAM after the proband's name) in the Augustine blood group system, encoded by the rare SLC29A1 variant allele AUG*04 (c.242A > G, p.Asn81Ser).

Sections du résumé

BACKGROUND
An antibody directed against a high-prevalence red blood cell (RBC) antigen was detected in a 67-year-old female patient of North African ancestry with a history of a single pregnancy and blood transfusion. So far, the specificity of the proband's alloantibody remained unknown in our immunohematology reference laboratory.
STUDY DESIGN AND METHODS
Whole-exome sequencing (WES) was performed on the proband's DNA. The reactivity to the SLC29A1-encoded ENT1 adenosine transporter was investigated by flow cytometry analyses of ENT1-expressing HEK293 cells, and RBCs from Augustine-typed individuals. Erythrocyte protein expression level, nucleoside-binding capacity, and molecular structure of the proband's ENT1 variant were further explored by western blot, flow cytometry, and molecular dynamics calculations, respectively.
RESULTS
A missense variant was identified in the SLC29A1 gene, which encodes the Augustine blood group system. It arises from homozygosity for a rare c.242A > G missense mutation that results in a nonsynonymous p.Asn81Ser substitution within the large extracellular loop of ENT1. Flow cytometry analyses demonstrated that the proband's antibody was reactive against HEK-293 cells transfected with control but not proband's SLC29A1 cDNA. Consistent with this finding, proband's antibody was found to be reactive with At(a-) (AUG:-2), but not AUG:-1 (null phenotype) RBCs. Data from structural analysis further supported that the proband's p.Asn81Ser variation does not alter ENT1 binding of its specific inhibitor NBMPR.
CONCLUSION
Our study provides evidence for a novel high-prevalence antigen, AUG4 (also called ATAM after the proband's name) in the Augustine blood group system, encoded by the rare SLC29A1 variant allele AUG*04 (c.242A > G, p.Asn81Ser).

Identifiants

pubmed: 36744388
doi: 10.1111/trf.17268
doi:

Substances chimiques

Blood Group Antigens 0
Isoantibodies 0

Types de publication

Case Reports Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

610-618

Informations de copyright

© 2023 AABB.

Références

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Auteurs

Cédric Vrignaud (C)

Université de Paris Cité, Inserm, BIGR, Paris, France.

Mahmoud Mikdar (M)

Université de Paris Cité, Inserm, BIGR, Paris, France.

Romain Duval (R)

Université de Paris Cité, Inserm, BIGR, Paris, France.
Centre National de Référence pour les Groupes Sanguins, Établissement Français de Sang (EFS), Paris, France.

Luc Reininger (L)

Université de Paris Cité, Inserm, BIGR, Paris, France.

Vijaya L Damaraju (VL)

Department of Oncology, University of Alberta, Edmonton, Alberta, Canada.

Michael Sawyer (M)

Cross Cancer Institute, Edmonton, Alberta, Canada.

Yves Colin (Y)

Université de Paris Cité, Inserm, BIGR, Paris, France.

Caroline Le Van Kim (C)

Université de Paris Cité, Inserm, BIGR, Paris, France.

Jean-Christophe Gelly (JC)

Université de Paris Cité, Inserm, BIGR, Paris, France.

Catherine Etchebest (C)

Université de Paris Cité, Inserm, BIGR, Paris, France.

Thierry Peyrard (T)

Université de Paris Cité, Inserm, BIGR, Paris, France.
Centre National de Référence pour les Groupes Sanguins, Établissement Français de Sang (EFS), Paris, France.

Slim Azouzi (S)

Université de Paris Cité, Inserm, BIGR, Paris, France.
Centre National de Référence pour les Groupes Sanguins, Établissement Français de Sang (EFS), Paris, France.

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