Nyberg Mia Titine, Stoevring Birgitte, Behr Elijah Raphael, Ravn Lasse Steen, McKenna William J, Christiansen Michael
Department of Clinical Biochemistry, Statens Serum Institut, Copenhagen, Denmark.
Clin Chim Acta. 2007 Jan;375(1-2):87-91. doi: 10.1016/j.cca.2006.06.020. Epub 2006 Jun 22.
Mutations in genes responsible for the cardiac action potential and control of intracellular Ca(2+)-distribution are associated with cardiac arrhythmia and sudden death. Sarcolipin is a 31-amino acid protein that inhibits the sarcoplasmic reticulum Ca(2+) ATPase pump (SERCA2). The sarcolipin gene, SLN, is expressed in the heart and a candidate gene for cardiomyopathy as well as atrial fibrillation (AF), long QT syndrome (LQTS) or sudden arrhythmic death syndrome (SADS). We examined the genetic variation of SLN in patients with the arrhythmic disorders AF, LQTS and SADS.
We screened the coding region of SLN for mutations using single strand conformation polymorphism/heteroduplex analysis on PCR-amplified genomic DNA from 95 unrelated LQTS patients, 59 SADS cases and 147 patients with atrial fibrillation (AF) and 92 controls. Aberrant conformers were sequenced.
No mutations or polymorphisms were found in the coding sequence. A G>C transition in the highly conserved position +1 of the 3'untranslated region (3'UTR) was found in two SADS cases. A polymorphism, a G>C transition at position -65 in the 5'untranslated region (5'UTR), was found with a G allele frequency of 0.48. A borderline significant difference in genotype distribution of the latter polymorphism was found between the AF group and controls.
Mutations in the coding region of SLN are not frequently involved in LQTS, SADS or AF. Whether the described 3'- and 5'UTR variants have functional significance must await further studies.
负责心脏动作电位及细胞内钙分布调控的基因突变与心律失常和猝死相关。肌浆球蛋白是一种由31个氨基酸组成的蛋白质,可抑制肌浆网钙ATP酶泵(SERCA2)。肌浆球蛋白基因(SLN)在心脏中表达,是心肌病、心房颤动(AF)、长QT综合征(LQTS)或心律失常性猝死综合征(SADS)的候选基因。我们研究了SLN在心律失常性疾病AF、LQTS和SADS患者中的基因变异情况。
我们采用单链构象多态性/异源双链分析,对来自95名无关的LQTS患者、59名SADS病例、147名心房颤动(AF)患者及92名对照者的PCR扩增基因组DNA进行分析,筛查SLN编码区的突变情况。对异常构象进行测序。
在编码序列中未发现突变或多态性。在2例SADS病例中,发现3'非翻译区(3'UTR)高度保守位置+1处有一个G>C转换。在5'非翻译区(5'UTR)位置-65处发现一个多态性,即G>C转换,G等位基因频率为0.48。在AF组与对照组之间,发现后一种多态性的基因型分布存在临界显著差异。
SLN编码区的突变在LQTS、SADS或AF中并不常见。所描述的3'和5'UTR变异是否具有功能意义,有待进一步研究。