Literature DB >> 17160941

[278C > T variant of the alpha-1, 3-galactosyltransferase allele responsible for Bw subgroup].

Xian-guo Xu1, Xiao-zhen Hong, Ying Liu, Jun-jie Wu, Kai-rong Ma, Fa-ming Zhu, Li-xing Yan.   

Abstract

OBJECTIVE: To investigate the molecular genetic basis of the Bw variant and identify novel alleles at ABO locus in Chinese Han population.
METHODS: Serological techniques were performed to characterize erythrocyte phenotype of a proband. Mutations of the ABO gene were screened by polymerase chain reaction, reverse transcription-polymerase chain reaction and DNA sequencing.
RESULTS: The proband was identified as Bw phenotype by serological technology and family study. A novel Bw variant allele was identified in the gDNA and cDNA. The novel allele was observed a missense mutation (278 C to T) at the exon 6 which resulted in an amino acid substitution (P93L) compared with B101 allele. The 278 C to T was the first report mutation position in exon 6 among Bw alleles, so the P93L amino acid substitution was different from others Bw variants which had amino acid substitutions in a conserved functional domain reported previously.
CONCLUSION: A novel Bw allele (278 C to T) responsible for Bw variant is reported in Chinese population.

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Year:  2006        PMID: 17160941

Source DB:  PubMed          Journal:  Zhonghua Yi Xue Yi Chuan Xue Za Zhi        ISSN: 1003-9406


  1 in total

1.  A Novel ABO Gene Variant Leads to Discrepant Results in Forward/Reverse and Molecular Blood Grouping.

Authors:  Meike Goebel; Ines Halm-Heinrich; Andreas Parkner; Gabriele Rink; Marcell U Heim; Peter Bugert
Journal:  Transfus Med Hemother       Date:  2013-10-27       Impact factor: 3.747

  1 in total

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