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利用聚合酶链反应和序列特异性引物对达菲基因中的突变进行快速单倍型分型。

Rapid haplotyping of mutations in the Duffy gene using the polymerase chain reaction and sequence-specific primers.

作者信息

Mullighan C G, Marshall S E, Fanning G C, Briggs D C, Welsh K I

机构信息

Nuffield Department of Surgery, Churchill Hospital, Headington, Oxford, United Kingdom.

出版信息

Tissue Antigens. 1998 Feb;51(2):195-9. doi: 10.1111/j.1399-0039.1998.tb02964.x.

Abstract

The molecular basis for the antigenic variation and red cell expression of the Duffy antigen system has recently been elucidated. We have developed a simple one-step method for genotyping the single nucleotide polymorphisms in the promoter and exon of the Duffy gene using the polymerase chain reaction and sequence-specific primers (PCR-SSP). This method is also capable of haplotyping alleles at the two polymorphisms as being in cis or trans orientation. Twenty-four serologically typed Caucasoid and Afro-Caribbean samples were examined to validate the method, with absolute correlation between phenotype and genotype. A further 30 Gambian samples were genotyped, confirming homozygosity for the FYnull-FYB haplotype. Allele, gene and haplotype frequencies were examined in 100 Caucasoid controls. This method permits the rapid genotyping of large numbers of samples and will prove useful as a clinical and research tool.

摘要

达菲抗原系统的抗原变异和红细胞表达的分子基础最近已被阐明。我们开发了一种简单的一步法,利用聚合酶链反应和序列特异性引物(PCR-SSP)对达菲基因启动子和外显子中的单核苷酸多态性进行基因分型。该方法还能够对两个多态性位点的等位基因进行单倍型分型,确定其顺式或反式排列。对24份经血清学分型的白种人和非洲加勒比海样本进行检测以验证该方法,结果显示表型与基因型之间具有绝对相关性。另外对30份冈比亚样本进行基因分型,证实为FY无效 - FYB单倍型纯合子。在100名白种人对照中检测了等位基因、基因和单倍型频率。该方法可对大量样本进行快速基因分型,将被证明是一种有用的临床和研究工具。

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