Literature DB >> 10765149

Polymorphisms of RhD(Va) and a new RhD(Va)-like variant found in Japanese individuals.

H Hyodo1, Y Ishikawa, K Kashiwase, A Ogawa, Y Watanabe, H Tsuneyama, C Toyoda, M Uchikawa, T Akaza, T Fujii, S Kozuma, Y Taketani, T Juji.   

Abstract

BACKGROUND AND OBJECTIVES: Red cell type RhD(Va) lacks epD1 and 5 and is encoded by hybrid RHD-CE(5)-D alleles. We analyzed RhD(Va) and RhD(Va)-like samples in Japanese blood donors.
MATERIALS AND METHODS: Ten RhD(Va) samples lacked epD1 and 5 and 3 RhD(Va)-like variants also lacked, epD2 and a part of 6/7. We identified the full-length nucleotide sequences of the complementary DNA (cDNA) synthesized from 4 samples: 3 of type D(Va) and the 4th a D(Va)-like variant.
RESULTS: Although their sequences differed from each other, all the substitutions were exclusively in exon 5. Three D(Va) samples had hybrid RHD-CE(5)-D alleles, but the D(Va)-like variant had a unique nucleotide substitution with a single amino acid change, E233K. Exon 5 of the genomic DNA from all 13 samples was analyzed by sequencing. No other sequences were identified.
CONCLUSION: All RhD(Va) and RhD(Va)-like variants had the substitution for E233. E233 seems to be a determinant of epD1 and 5. A new category of RhD variant, DYO, was identified.

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Year:  2000        PMID: 10765149     DOI: 10.1159/000031162

Source DB:  PubMed          Journal:  Vox Sang        ISSN: 0042-9007            Impact factor:   2.144


  2 in total

1.  Whole exon 5 and intron 5 replaced by RHCE in DVa(Hus).

Authors:  Chaopeng Shao; Wen Xiong; Wei Wang
Journal:  J Hum Genet       Date:  2004-01-09       Impact factor: 3.172

2.  D category IV: a group of clinically relevant and phylogenetically diverse partial D.

Authors:  Inge von Zabern; Franz F Wagner; Joann M Moulds; John J Moulds; Willy A Flegel
Journal:  Transfusion       Date:  2013-03-05       Impact factor: 3.157

  2 in total

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