Müller-Steinhardt Michael, Schulte Friederike, Klüter Harald, Bugert Peter
Institute of Transfusion Medicine and Immunology, Medical Faculty Mannheim, Heidelberg University, Friedrich-Ebert-Strasse 107, 68167 Mannheim, Germany, DRK-Blutspendedienst Baden-Württemberg - Hessen, Germany.
BMC Res Notes. 2009 Dec 10;2:245. doi: 10.1186/1756-0500-2-245.
Interleukin-6 (IL-6) promoter polymorphisms at positions -597(G-->A), -572(G-->C) and -174(G-->C) were shown to have a clinical impact on different major diseases. At present PCR-SSP protocols for IL-6 -597/-572/-174haplotyping are elaborate and require large amounts of genomic DNA.
We describe an improved typing technique requiring a decreased number of PCR-reactions and a reduced PCR-runtime due to optimized PCR-conditions.
This enables a fast and efficient determination of IL-6 -597/-572/-174haplotypes in clinical diagnosis and further evaluation of IL-6 promoter polymorphisms in larger patient cohorts.
白细胞介素-6(IL-6)启动子在-597(G→A)、-572(G→C)和-174(G→C)位置的多态性已显示对不同的主要疾病有临床影响。目前用于IL-6 -597/-572/-174单倍型分型的PCR-SSP方案很复杂,需要大量的基因组DNA。
我们描述了一种改进的分型技术,由于优化了PCR条件,该技术所需的PCR反应数量减少且PCR运行时间缩短。
这使得在临床诊断中能够快速、高效地确定IL-6 -597/-572/-174单倍型,并在更大的患者队列中进一步评估IL-6启动子多态性。