애스크로AIPublic Preview
← 학술논문 검색
학술논문Annals of Laboratory Medicine2010.02 발행KCI 피인용 2

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

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

조덕(전남대학교); 신동준(화순전남대학교병원); Mark Harris Yazer(University of Pittsburgh, Pittsburgh, USA); 임춘화(을지대학교); 허영문(Severans Women’s Clinic); 기승정(전남대학교 의과대학 진단검사의학교실); 김수현(전남대학교); 신명근(전남대학교); 신종희(전남대학교); 서순팔(전남대학교); 양동욱(전남대학교)

30권 1호, 65~69쪽

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)

발행기관:
대한진단검사의학회
분류:
병리학

AI 법률 상담

이 논문의 주제에 대해 더 알고 싶으신가요?

460만+ 법률 자료에서 관련 판례·법령·해석례를 찾아 답변합니다

AI 상담 시작
The M142T Mutation Causes B3 Phenotype: Three Cases and an in vitro Expression Study | Annals of Laboratory Medicine 2010 | AskLaw | 애스크로 AI