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Analysis for 2 samples with HLA-DQB1 allele dropout at exon 2 in sequence-based typing / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 496-498, 2014.
Artigo em Chinês | WPRIM | ID: wpr-291744
ABSTRACT
<p><b>OBJECTIVE</b>To explore the reason for HLA-DQB1 allele dropout during routine sequence-based typing(SBT) in order to improve the accuracy of typing.</p><p><b>METHODS</b>Two thousand samples derived from HLA high-resolution typing laboratory were typed for HLA-DQB1 locus using an AlleleSEQR HLA-DQB1 SBT kit. Non-conclusive results and "abnormal" sequencing samples were retyped using a LABType rSSO HD HLA-DQB1 kit and further analyzed with both sequence-specific primers and group-specific primers and sequenced for haplotype analysis.</p><p><b>RESULTS</b>Among the 2000 samples, 2 samples with no conclusive result were identified. The heterozygosity was confirmed with both the LAB Type SSO HD HLA-DQB1 kit and PCR-SBT in house method. Subsequent HLA-DQB1 cloning and haplotype sequencing have elucidated that HLA-DQB1*0202 dropped out at exon 2 for the first sample and HLA-DQB1*020101 dropped out at exon 2 for the second sample during PCR amplification. No novel nucleotide mutation was found.</p><p><b>CONCLUSION</b>Our results indicated that preferential amplification at exon 2 of DQB1 may result in allele dropout in exon 2 sequences during HLA-DQB1 SBT test. This may provide useful information for HLA genotyping.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Teste de Histocompatibilidade / Reação em Cadeia da Polimerase / Éxons / Primers do DNA / Alelos / Cadeias beta de HLA-DQ / Genética / Genótipo / Métodos Limite: Humanos Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2014 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Teste de Histocompatibilidade / Reação em Cadeia da Polimerase / Éxons / Primers do DNA / Alelos / Cadeias beta de HLA-DQ / Genética / Genótipo / Métodos Limite: Humanos Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2014 Tipo de documento: Artigo