Eckhardt Lee L, Farley Amanda L, Rodriguez Esther, Ruwaldt Karen, Hammill Daniel, Tester David J, Ackerman Michael J, Makielski Jonathan C
Department of Medicine (Cardiovascular Medicine), University of Wisconsin, Madison, WI 53792, USA.
Heart Rhythm. 2007 Mar;4(3):323-9. doi: 10.1016/j.hrthm.2006.10.025. Epub 2006 Nov 10.
Loss-of-function mutations in the KCNJ2 cause approximately 50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features. Do KCNJ2 mutations occur in patients lacking this triad and lacking a family history of ATS?
The purpose of this study was to identify and characterize mutations in the KCNJ2-encoded inward rectifier potassium channel Kir2.1 from patients referred for genetic arrhythmia testing.
Mutational analysis of KCNJ2 was performed for 541 unrelated patients. The mutations were made in wild type (WT) and expressed in COS-1 cells and voltage clamped for ion currents.
Three novel missense mutations (R67Q, R85W, and T305A) and one known mutation (T75M) were identified in 4/249 (1.6%) patients genotype-negative for other known arrhythmia genes with overall incidence 4/541 (0.74%). They had prominent U-waves, marked ventricular ectopy, and polymorphic ventricular tachycardia but no facial/skeletal abnormalities. Periodic paralysis was present in only one case. Outward current was decreased to less than 5% of WT for all mutants expressed alone. Co-expression with WT (simulating heterozygosity) caused a marked dominant negative effect for T75M and R82W, no dominant negative effect for R67Q, and a novel selective enhancement of inward rectification for T305A.
KCNJ2 loss of function mutations were found in approximately 1% of patients referred for genetic arrhythmia testing that lacked criteria for ATS. Characterization of three new mutations identified a novel dominant negative effect selectively reducing outward current for T305A. These results extend the range of clinical phenotype and molecular phenotype associated with KCNJ2 mutations.
KCNJ2基因功能丧失性突变导致约50%的安德森-陶威尔综合征(ATS),其特征为周期性瘫痪、室性心律失常和畸形特征的经典三联征。KCNJ2突变是否发生在缺乏该三联征且无ATS家族史的患者中?
本研究的目的是鉴定和表征因遗传性心律失常检测而转诊患者的KCNJ2编码内向整流钾通道Kir2.1中的突变。
对541名无亲缘关系的患者进行KCNJ2突变分析。在野生型(WT)中进行突变,并在COS-1细胞中表达,通过电压钳记录离子电流。
在4/249(1.6%)名其他已知心律失常基因基因型阴性的患者中鉴定出三个新的错义突变(R67Q、R85W和T305A)和一个已知突变(T75M),总体发生率为4/541(0.74%)。他们有明显的U波、显著的室性早搏和多形性室性心动过速,但无面部/骨骼异常。仅1例出现周期性瘫痪。单独表达时,所有突变体的外向电流均降至野生型的5%以下。与野生型共表达(模拟杂合性)时,T75M和R82W产生明显的显性负效应,R67Q无显性负效应,T305A则出现内向整流的新型选择性增强。
在因遗传性心律失常检测而转诊且缺乏ATS标准的患者中,约1%发现了KCNJ2功能丧失性突变。对三个新突变的表征确定了T305A选择性降低外向电流的新型显性负效应。这些结果扩展了与KCNJ2突变相关的临床表型和分子表型范围。