Akkad D A, Arning L, Ibrahim S M, Epplen J T
Department of Human Genetics, Ruhr University, Bochum, Germany.
Genes Immun. 2007 Dec;8(8):703-6. doi: 10.1038/sj.gene.6364429. Epub 2007 Sep 13.
The interleukin 4 promoter polymorphism -589 C/T (rs2243250) was genotyped in 869 multiple sclerosis (MS) patients and 595 healthy blood donors. Sex-specific MS association was evident whereas two flanking polymorphisms showed insignificant P values. In dual luciferase assays of cultured Jurkat cells the cloned promoter comprising the -589 T allele leads to higher expression as compared to the respective construct with the C allele. Together these findings may be discussed functionally as contributing to the genetic predisposition and to the pathogenesis in MS.
在869例多发性硬化症(MS)患者和595名健康献血者中对白细胞介素4启动子多态性-589 C/T(rs2243250)进行了基因分型。性别特异性的MS关联很明显,而两个侧翼多态性的P值无统计学意义。在培养的Jurkat细胞的双荧光素酶测定中,与含有C等位基因的相应构建体相比,包含-589 T等位基因的克隆启动子导致更高的表达。综合这些发现,从功能角度来看,可能有助于MS的遗传易感性和发病机制。