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Transfusion ; 58(4): 1054-1064, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29399809

RESUMO

BACKGROUND: The P1 /P2 phenotypic polymorphism is one of the earliest blood groups discovered in humans. These blood groups have been connected to different levels of expression of the A4GALT gene in P1 and P2 red blood cells; however, the detailed molecular genetic mechanism that leads to these two phenotypes has not been established. STUDY DESIGN AND METHODS: After our previous identification of an association between the single-nucleotide polymorphisms (SNPs) rs2143918 and rs5751348 in A4GALT gene and the P1 /P2 phenotype, we conduct a survey of transcription factors that might connect these SNPs with the differential expression of the P1 -A4GALT and P2 -A4GALT alleles. An in silico analysis of potential transcription factor binding motifs within the polymorphic SNPs rs2143918 and rs5751348 genomic regions was performed, and this was followed by reporter assays examining the candidate transcription factors, gene expression profiling, electrophoretic mobility shift assays, and P1 -A4GALT and P2 -A4GALT allelic expression analysis. RESULTS: The results revealed that the differential binding of transcription factor early growth response 1 to the SNP rs5751348 genomic region with the different genotypes in the A4GALT gene leads to differential activation of P1 -A4GALT and P2 -A4GALT expression. CONCLUSION: The present investigation, together with our previous study (Lai et al., Transfusion 2014;54:3222-31), have elucidated the molecular genetic details associated with the P1 /P2 blood groups.


Assuntos
Proteína 1 de Resposta de Crescimento Precoce/fisiologia , Galactosiltransferases/biossíntese , Regulação da Expressão Gênica , Polimorfismo de Nucleotídeo Único , Alelos , Simulação por Computador , Fatores de Transcrição de Resposta de Crescimento Precoce/fisiologia , Ensaio de Desvio de Mobilidade Eletroforética , Galactosiltransferases/genética , Perfilação da Expressão Gênica , Genes Reporter , Células HEK293 , Humanos , Ligação Proteica , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/genética , Transcrição Gênica
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