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The M142T Mutation Causes B3 Phenotype: Three Cases and an in vitro Expression Study / 대한진단검사의학회지
The Korean Journal of Laboratory Medicine ; : 65-69, 2010.
Article in English | WPRIM | ID: wpr-82766
ABSTRACT
The B3 phenotype is the most common B subtype in Korea. The B305 allele (425 T>C, M142T) was first reported in 2 Chinese individuals; however, it has not yet been reported in the Koreans, and the impact of the M142T mutation on the expression of the B3 phenotype has also not been studied. To resolve an ABO discrepancy between a group O neonate and her group O father and A(1)B(3) mother, blood samples from these individuals and other family members were referred to our laboratory for ABO gene analysis. The B305 allele was discovered in the neonate (B305/O01), her mother (A102/ B305), and her maternal aunt (B305/O02), while her father was typed as O01/O02. Transient transfection experiments were performed in HeLa cells using the B305 allele synthesized by site-directed mutagenesis; flow cytometric analysis revealed that this transfect expressed 35.5% of the total B antigen produced by the B101 allele transfect. For comparison, Bx01 allele transfects were also created, and they expressed 11.4% of the total B antigen expressed on the surface of B101 transfects. These experiments demonstrate that the M142T (425 T>C) mutation is responsible for the B subtype phenotype produced by the B305 allele.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / ABO Blood-Group System / HeLa Cells / Transfection / Gene Expression Regulation / Sequence Analysis, DNA / Amino Acid Substitution / Polymorphism, Single Nucleotide / Alleles / Flow Cytometry Type of study: Etiology study Limits: Adult / Child / Female / Humans Language: English Journal: The Korean Journal of Laboratory Medicine Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / ABO Blood-Group System / HeLa Cells / Transfection / Gene Expression Regulation / Sequence Analysis, DNA / Amino Acid Substitution / Polymorphism, Single Nucleotide / Alleles / Flow Cytometry Type of study: Etiology study Limits: Adult / Child / Female / Humans Language: English Journal: The Korean Journal of Laboratory Medicine Year: 2010 Type: Article