Soejima Mikiko, Koda Yoshiro
Department of Forensic Medicine, Kurume University School of Medicine, Kurume, 830-0011, Japan.
Electrophoresis. 2021 Feb;42(3):315-318. doi: 10.1002/elps.202000241. Epub 2020 Nov 22.
The secretor status of ABH antigens, determined by FUT2 polymorphisms, affects susceptibility to various infectious diseases. In addition to many SNPs responsible for the nonsecretor phenotype, five nonfunctional alleles (se) resulting from copy number variations have been reported. One of the five alleles generated by an unequal crossover between FUT2 and a pseudogene (SEC1), is se . This allele may be misidentified as a functional allele if only common inactivating SNPs are genotyped because it contains the 3' region of the functional FUT2. Therefore, accurate detection of se is desirable. For this purpose, a high-resolution melting (HRM) analysis is developed for detection of se in which a 284bp fragment of SEC1 and se but not FUT2, are amplified. This HRM analysis detected se reliably. Thus, an initial screening or prescreening for se using HRM analysis seems to be useful for association studies of FUT2.
由FUT2基因多态性决定的ABH抗原分泌状态,会影响对各种传染病的易感性。除了许多导致非分泌型表型的单核苷酸多态性(SNP)外,还报道了由拷贝数变异产生的五个无功能等位基因(se)。由FUT2和一个假基因(SEC1)之间不等交换产生的五个等位基因之一是se。如果仅对常见的失活SNP进行基因分型,该等位基因可能会被误鉴定为功能等位基因,因为它包含功能性FUT2的3'区域。因此,需要准确检测se。为此,开发了一种高分辨率熔解(HRM)分析方法来检测se,其中扩增SEC1和se的284bp片段,但不扩增FUT2。这种HRM分析能够可靠地检测se。因此,使用HRM分析对se进行初步筛查或预筛查,似乎对FUT2的关联研究有用。