본문 바로가기
KERD
논문KCI 등재

The M142T Mutation Causes B3 Phenotype: Three Cases and an in vitro Expression Study

2

조회

0

다운로드

2

인용

0

참고문헌

키워드

주제분류병리학

초록

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 A1B3 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. (Korean J Lab Med 2010;30:65-9)

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 A1B3 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. (Korean J Lab Med 2010;30:65-9)

참고문헌 (18)

  1. Yamamoto F, "Hakomori S. Molecular genetic basis of the histo-blood group ABO system", Nature, 345, pp.229~233 (1990)
  2. Yamamoto F, "Cloning and characterization of DNA complementary to human UDP-GalNAc: Fuc alpha 1----2Gal alpha 1----3GalNAc transferase (histo-blood group A transferase) mRNA", J Biol Chem, 265, pp.1146~1151 (1990)
  3. Yu LC, "Molecular genetic analysis for the B(3) allele", Blood, 100, pp.1490~1492 (2002)
  4. Olsson ML, "Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles", Blood, 98, pp.1585~1593 (2001)
  5. Ogasawara K, "Molecular genetic analysis of variant phenotypes of the ABO blood group system", Blood, 88, pp.2732~2737 (1996)
  6. Cho D, "A novel B(var) allele (547 G>A) demonstrates differential expression depending on the co-inherited ABO allele", Vox Sang, 87, pp.187~189 (2004)
  7. Seo DH, "ABO gene analysis of cis-AB and B subgroup in blood donors", Korean J Blood Transfus, 11, pp.27~34 (2000)
  8. Lee SG, "Analysis of complete exons and flanking introns of ABO gene in Korean B(3) blood donors", Korean J Blood Transfus, 17, pp.97~105 (2006)
  9. Xu XG, "A novel M142T mutation in the B glycosyltransferase gene associated with B3 variant in Chinese", Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 26, pp.254~257 (2009)
  10. Yamamoto F, "Molecular genetic analysis of the ABO blood group system: 3. A(X) and B(A) alleles", Vox Sang, 64, pp.171~174 (1993)
  11. Ogasawara K, "Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes", Immunogenetics, 53, pp.190~199 (2001)
  12. Yazer MH, "ABO sequence analysis in a family with weak expression of blood group B", Transfusion, 44, pp.1394~1395 (2004)
  13. Brecher ME, "Technical manual. 14th ed", pp.670~671 (2002), American Association of Blood Banks
  14. Cho D, "The genetic and phenotypic basis of blood group A subtypes in Koreans", Transfus Med, 15, pp.329~334 (2005)
  15. Seltsam A, "Hallensleben M, Kollmann A, Blasczyk R. The nature of diversity and diversification at the ABO locus", Blood, 102, pp.3035~3042 (2003)
  16. 조덕, "ABO 유전형 검사에 의한 ABO 불일치의 해결", The Korean Journal of Laboratory Medicine, 26(2), pp.107~113 (2006), 대한진단검사의학회
  17. Seltsam A, "Missense mutations outside the catalytic domain of the ABO glycosyltransferase can cause weak blood group A and B phenotypes", Transfusion, 45, pp.1663~1669 (2005)
  18. Seltsam A, "Das Gupta C, Bade-Doeding C, Blasczyk R. A weak blood group A phenotype caused by a translation-initiator mutation in the ABO gene", Transfusion, 46, pp.434~440 (2006)

관련 논문AI추천

이 간행물의 다른 논문 (15건)