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[Molecular genetic analysis for the A3 alleles].
Yu, Qiong; Liang, Yan-Lian; Deng, Zhi-Hui; Wu, Guo-Guang; Su, Yu-Qing; Zhang, Xuan; Chen, Liang-Hong.
Afiliação
  • Yu Q; Shenzhen Blood Center, Shenzhen Institute of Transfusion Medicine, Shenzhen 518035, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 13(1): 135-9, 2005 Feb.
Article em Zh | MEDLINE | ID: mdl-15748453
ABSTRACT
To study four A(3) subgroup samples identified by serologic tests, among which two belong to a family, three were A(3) subgroup, one was A(3)B subgroup. All four samples were genotyped by PCR-SSP method, and the nucleotide sequences of Exon 6, Exon 7 and part introns at the ABO locus for these samples were detected by ABI Prism 3100 DNA sequencer. Comparison with the consensus of A101 was performed. The results showed that haplotypes of two A(3) subgroups were common A102 allele and O1-2 allele, and haplotypes of one A(3) subgroup were common A102 allele and rare O(1v)-4 allele. Unexpectedly, a synonymous substitution 838C-->T had been found in A allele of the A(3)B subgroup sample, which predict a Leu280Phe alteration. The results suggested that molecular genetic background of the A(3) phenotypes is polymorphic. Possibly, the missense mutation 838C-->T is the molecular genetic basis of A(3)B subgroup that lead to low activity of the glycosyltransferases.
Assuntos
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Base de dados: MEDLINE Assunto principal: Sistema ABO de Grupos Sanguíneos / Povo Asiático / Alelos / Mutação Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: Asia Idioma: Zh Ano de publicação: 2005 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Sistema ABO de Grupos Sanguíneos / Povo Asiático / Alelos / Mutação Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: Asia Idioma: Zh Ano de publicação: 2005 Tipo de documento: Article