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GP.MOT: A novel glycophorin variant identified in a Japanese blood donor.
Oda, Akira; Suzuki, Yumi; Isa, Kazumi; Ogasawara, Kenichi; Yabe, Ryuichi; Kimura, Takafumi; Uchikawa, Makoto; Tsuno, Nelson Hirokazu.
Afiliación
  • Oda A; Laboratory, Japanese Red Cross Kanto-Koshinetsu Block Blood Center, Tokyo, Japan.
  • Suzuki Y; Laboratory, Japanese Red Cross Kinki Block Blood Center, Osaka, Japan.
  • Isa K; Laboratory, Japanese Red Cross Kanto-Koshinetsu Block Blood Center, Tokyo, Japan.
  • Ogasawara K; Blood Group Research Unit, Japanese Red Cross Central Blood Institute, Tokyo, Japan.
  • Yabe R; Blood Group Research Unit, Japanese Red Cross Central Blood Institute, Tokyo, Japan.
  • Kimura T; Laboratory, Japanese Red Cross Kanto-Koshinetsu Block Blood Center, Tokyo, Japan.
  • Uchikawa M; Laboratory, Japanese Red Cross Kinki Block Blood Center, Osaka, Japan.
  • Tsuno NH; Laboratory, Japanese Red Cross Kanto-Koshinetsu Block Blood Center, Tokyo, Japan.
Transfusion ; 61(10): 2825-2829, 2021 10.
Article en En | MEDLINE | ID: mdl-34369596
BACKGROUND: In this study, we identified a novel glycophorin variant (GP.MOT) in a Mia -positive Japanese blood donor. The proband with this glycophorin variant was discovered by antigen screening of samples from 475,493 Japanese blood donors using monoclonal anti-Mia . STUDY DESIGN AND METHODS: Standard serological techniques and flow cytometry were performed. GP.MOT RBCs were examined by immunoblotting using anti-GPA, anti-MUT or anti-Mur. Genome DNA was extracted from whole blood, and the GYPA/GYPB was analyzed by polymerase chain reactions and Sanger sequencing. RESULTS: The MNS blood group of the proband was M + N + w S-s + with the presence of other low-frequency antigens including Mia , Mur, MUT, and KIPP. A 43-kDa molecule, which is almost equivalent in size to glycophorin A (GPA), was identified by immunoblotting using monoclonal anti-MUT and anti-Mur. Sanger sequencing clearly indicated that the proband had two different GYPA*M alleles at SNP rs62334651 (GYPA*M232 + 55A and GYPA*M232 + 55G), as well as a GYP(B-A) hybrid allele (GYP*MOT) with breakpoints located on pseudoexon 3 of GYPB from c.210 to c.219. DISCUSSION: We identified a hybrid glycophorin GP.MOT with the deduced unique amino acid sequence GPB (20-45)-GPΨB (46-70)-GPA (71-149), which has not been previously reported.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glicoforinas Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Transfusion Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glicoforinas Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Transfusion Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos