von Kodolitsch Y, Berger J, Rogan P K
Department of Cardiology, University Hospital Eppendorf, Hamburg, Germany.
Haemophilia. 2006 May;12(3):258-62. doi: 10.1111/j.1365-2516.2006.01216.x.
Bleeding symptoms and clotting activity vary among mutations that alter mRNA splicing of either the factor VIII or factor IX genes. We analyzed splicing mutations in both genes for changes in individual information (R(i), in bits) involving both donor or acceptor sites. Mutations with low or negative R(i) values (<2.4 bits) or significant changes in R(i) (DeltaR(i) > or = 7 bits) exhibited either reduced protein activity, increased clotting time and bleeding frequency and were predictive of severe disease. Thus, information analysis of splicing mutations may be useful in predicting phenotypes in hemophilia.
改变凝血因子VIII或凝血因子IX基因mRNA剪接的突变,其出血症状和凝血活性各不相同。我们分析了这两个基因中的剪接突变,以了解涉及供体或受体位点的个体信息(以比特为单位的R(i))的变化。R(i)值低或为负(<2.4比特)或R(i)有显著变化(ΔR(i)≥7比特)的突变,要么蛋白活性降低,要么凝血时间延长、出血频率增加,并且可预测严重疾病。因此,剪接突变的信息分析可能有助于预测血友病的表型。