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. 2011 Dec 30;7(6):941–947. doi: 10.5114/aoms.2011.26604

Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2

Ewa Moric-Janiszewska 1, Joanna Głogowska-Ligus 2, Monika Paul-Samojedny 3, Ludmiła Węglarz 1, Grażyna Markiewicz-Łoskot 4, Lesław Szydłowski 5
PMCID: PMC3264984  PMID: 22328875

Abstract

Introduction

The main goal of this study was to examine the patient age and sex dependent expression of KCNQ1 and HERG genes that encode potassium channels responsible for the occurrence of long QT syndrome (LQTS).

Material and methods

The study enrolled 43 families whose members suffered from LQTS type 1 (LQTS1) or 2 (LQTS2) or were healthy. The study attempted to prove that β-actin is a good endogenous control when determining the expression of the studied genes. Examination of gene expression was achieved with quantitative real-time PCR (QRT-PCR). Expression of the investigated genes was inferred from the analysis of the number of mRNA copies per 1 μg total RNA isolated from whole blood.

Results

Significantly lower KCNQ1 and KCNH2 mRNA levels in healthy females than healthy males were observed (p = 0.032; p = 0.02). In male patients both transcripts were expressed at a lower level (p = 0.0084; p = 0.035). The comparison of transcriptional activity of KCNQ1 and KCNH2 in healthy adults and children revealed higher KCNQ1 and lower KCNH2 mRNA levels in healthy adults (p = 0.033; p = 0.04), higher KCNQ1 and lower KCNH2 mRNA levels in adult patients below 55 years old than in adults over 55 years old (p=0.036; p = 0.044), and significantly higher KCNQ1 and lower KCNH2 mRNA levels in adult patients (over 55 years) than in paediatric patients (below 15 years) (p=0.047; p = 0.08).

Conclusions

The results support the hypothesis that KCNQ1 and HERG gene expression is influenced by age and gender in human patients with long QT syndrome and in healthy subjects.

Keywords: long QT syndrome, KCNQ1 gene, HERG gene, expression, potassium channel

Introduction

Genetic disorder is an important cause of sudden cardiac death (SCD) in children without structural heart diseases [1, 2]. However, the risk in affected patients is not uniform because of variable penetrance and is influenced by age, gender, genotype, environmental factors, therapy, and possibly other modifier genes [3]. In recent years, numerous advances have been made in the identification of the genotype-phenotype relationship and risk factors for cardiac events in long QT syndrome (LQTS) patients [1, 4–10].

Hereditary long QT syndrome (LQTS) is characterized by prolonged ventricular repolarization on the ECG and arrhythmia-related syncope and sudden death [3, 11–13]. Mutations in several ion channel genes are known to cause this disorder 14, mutations in the KCNQ1 gene causing type-1 long QT syndrome [15, 16] and in the human ether-a-go-go-related gene (HERG) causing type-2 long QT syndrome [17]. Mutations involving the KCNQ1 gene result in reduction of the slow component of the delayed rectifier repolarizing current IKs, HERG mutations have been found to be associated with reduction of the rapid component of this current IKr, and both contribute to lengthening of the QT interval [15, 18]. In humans the KCNQ1 gene is expressed in kidneys, placenta, lungs and heart. The highest mRNA transcript levels of the KCNQ1 gene have been observed in heart muscle cells; no expression was found in brain, skeletal muscles or liver [19, 20]. The KCNH2 gene was shown to be important in preventing premature heart stimulation [21, 22].

The aim of this study was to answer the question how the expression of genes encoding slow and fast potassium channels, KCNQ1 and HERG, respectively, changes depending on age and gender of the patient.

Material and methods

Gene expression was studied in subjects from unrelated families; initial diagnoses were based on such clinical features as altered ECG and echocardiography. One hundred sixty-three patients from the Paediatric Cardiology Department of the Medical University of Silesia in Katowice-Ligota were enrolled in the study, including 98 with clinically diagnosed (ECG) LQTS. Type 1 LQTS was diagnosed in 60 patients and type 2 LQTS in 38 patients. The remaining 65 patients were healthy individuals without clinically confirmed LQTS symptoms; these individuals were from 43 families whose members were diagnosed with the long QT syndrome. The principal goal of this study was to examine the expression of KCNQ1 and HERG genes that are responsible for the occurrence of LQTS1 and LQTS2. Additionally, the study attempted to answer the question whether and how the expression of the examined genes depends on patients’ age and gender. The study also attempted to verify whether β-actin is a good endogenous control for determining the expression of the studied genes.

Total RNA extraction

Total RNA extraction was performed using Fenozol total RNA isolation Reagent Set (A&A Biotechnology). Consent to use blood samples taken from patients was obtained from the Bioethics Committee of the MUS in Katowice.

QRT-PCR

Assessment of transcriptional activity of the investigated genes was carried out using commercial kits (TaqMan Gene Expression Assays Applera for KCNQ1 gene inventoried set 4331182 Hs00165003m1 – length of PCR product 78 bp; for HERG gene inventoried set 4331182 Hs00542478m1 – length of PCR product 82 bp). The number of mRNA copies of the investigated genes was determined based on kinetics of the QRT-PCR reaction using an ABI PRISM™ 7000 sequence detector (Applied Biosystems, CA, USA) and a ROX QuantiTect Probe RT-PCR kit containing a fluorescent dye. QRT-PCR was carried out in one step. The reaction mix contained 10 μl 2×QuantiTect Probe RT-PCR Master Mix, 0.1 μl QuantiTect RT Mix (Qiagen GmbH, Germany) and 1 μl mix of TaqMan Gene Expression Assay starters and probes (Applied Biosystems), RNA matrix and pyrogen-free water. The reaction mix to amplify β-actin gene DNA standards contained 25 μl 2×QuantiTect Probe RT-PCR Master Mix (Qiagen GmbH, Germany) and 0.5 μM sense and antisense starters, β-actin cDNA template and pyrogen-free water (Applied Biosystems TaqMan Gene Expression Assays for AKT 4331182 Hs 99999903_m1). The reverse transcription reaction (in two repeats) was carried out at 50°C for 30 min. Following initial activation of HotStar Taq DNA Polymerase (95°C/15 min), a two-step reaction was carried out including denaturation at 94°C for 15 s and starter annealing at 60°C for 60 s (40 cycles). Final elongation of amplification products was carried out at 72°C for 10 min. To confirm the absence of non-specific amplification, the PCR products were analysed by polyacrylamide gel electrophoresis and sequence analysis (ABIPRISM377).

Statistical analysis

Expression level of the investigated genes was inferred from the analysis of the number of mRNA copies per 1 μg total RNA. The data were exported from an Excel datasheet to the STATISTICA v.7.1 data analysis software system (StatSoft Inc. 2006). Descriptive statistics were computed including median, standard deviation and average values. The degree of normality was examined with the Shapiro-Wilk test. Due to the lack of normal distribution of the investigated parameters, we used a non-parametric test (Mann-Whitney U-test) to analyse the results from the experimental and control groups. The statistical significance level was set at p < 0.05.

Results

A series of QRT-PCR reactions was performed. The electrophoretic evaluation of amplimers (length of PCR product for KCNQ1 gene – 78 bp; for HERG gene – 82 bp) and sequence analysis confirmed the specificity of the performed QRT-PCR reaction (data not shown). The results are expressed as the number of mRNA copies of the analysed genes per 1 μg of total RNA. We have determined β-actin mRNA copy number in all analysed groups. The β-actin mRNA copy numbers were not statistically different between control and affected groups and may be a good endogenous control for determining the expression of the studied genes.

Significantly lower KCNQ1 and KCNH2 mRNA levels in healthy females than healthy males were observed (Mann-Whitney U test, p = 0.032; p = 0.02; Figure 1), whereas in male patients both transcripts were expressed at a lower level than in female patients (Mann-Whitney U test, p = 0.0084; p = 0.035; Figure 2). The comparison of transcriptional activity of KCNQ1 and KCNH2 genes in healthy adults and childmale patients (Mann-Whitney U test, p=0.0084; p=0.035; Figure 2). The comparison of transcriptional activity of KCNQ1 and KCNH2 genes in healthy adults and children revealed considerably higher KCNQ1 and lower KCNH2 mRNA levels in healthy adults (Mann-Whitney U test, p=0.033; p=0.04; Figure 3).

Figure 1.

Figure 1

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Comparison of KCNQ1 and KCNH2 mRNA levels between healthy females and males. Results are expressed as copy numbers per 1 µg of total RNA

Figure 2.

Figure 2

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Comparison of KCNQ1 and KCNH2 mRNA levels between female and male patients. Results are expressed as copy numbers per 1 µg of total RNA

Figure 3.

Figure 3

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Comparison of KCNQ1 and KCNH2 mRNA levels between healthy adults and healthy children. Results are expressed as copy numbers per 1 µg of total RNA

We have also compared KCNQ1 and KCNH2 mRNA copy numbers in patient groups divided into subgroups based on their age (adults – age below 55 years and over 55 years; children – age below 15 and over 15 years). This analysis showed remarkably higher KCNQ1 and lower KCNH2 mRNA levels in adult patients below 55 years old than in adults over 55 years old (Mann-Whitney U test, p=0.036; p=0.044; Figure 4).

Figure 4.

Figure 4

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Comparison of KCNQ1 and KCNH2 mRNA levels between adults patients (age > 55 years and age < 55 years). Results are expressed as copy numbers per 1 µg of total RNA

Moreover, significantly higher KCNQ1 and lower KCNH2 mRNA levels were detected in adult patients (age over 55 years) than in paediatric patients (age below 15 years) (Mann-Whitney U test, p=0.047; p=0.08; Figure 5).

Figure 5.

Figure 5

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Comparison of KCNQ1 and KCNH2 mRNA levels of adult patients (age > 55 years) and paediatric patients (age < 15 years). Results are expressed as copy numbers per 1 µg of total RNA

Discussion

The existence of differences in heart rhythm disorders in women compared to men has been known at least since 1996, when Burke et al. [23] described electrocardiographic changes in the form of prolonged QT duration, higher incidence of sinus rhythm at rest, and the tendency to recurrent nodal tachycardia or a medication-induced ventricular tachycardia torsades de pointes (TdP) [24]. In women, a prolonged QT interval (also corrected), on average by 10-20 ms compared to that of men, and shorter QT dispersion have been confirmed [25, 26]. There has also been proven higher incidence of complications and pro-arrhythmic effect of various drugs such as antihistamines, antibiotics (erythromycin), antiarrhythmics (sotalol), antidepressants and others. The ability of these drugs to block potassium channels suggests still undefined dysfunction of these channels in women [27, 28]. The studies of Rautaharju et al. [29] have also confirmed that the QTc interval is longer in women than in men aged 15-55 years, while no differences were observed in corrected QTc duration in children up to 15 years old and adults over 55 years old. There are several explanations for the mechanisms responsible for QT prolongation and a tendency to arrhythmia in women. These include very low level of androgens with their protective effect and consequently decreased QTc as opposed to men, genetically based differences in the density of potassium channels in the cell membrane of myocardial cells, modulating effects of oestrogens on the function and kinetics of potassium and calcium channels, modulating the expression of ion channels [30–34], and prolongation of QTc as well as dominance of the parasympathetic system favouring the extension of the QT [35, 37]. The study by Liu et al. [32] suggests low expression of genes encoding potassium channels in female rabbit myocardium cells compared with male rabbits (density of potassium channels lower by 20%, cellular Ik1 potassium currents lower by 14%). Besides the differences in the duration of the QT interval between women and men, also differences in the dynamics of adaptation of QT duration to heart rate changes, as well as differences in the morphology of ST-T segments have been observed. They result from lower heart muscle weight, dissimilar thorax configuration and probably different ionic structure of cell membrane of heart muscle in women compared to men [32, 38]. Further studies revealed that among patients reported to the international registry of patients with cLQTS women constituted 70% of the probands [4, 5, 31, 39, 40]. Moss et al. [41] have proposed criteria for diagnosis of QT prolongation specific to gender and age of the test: for children aged 0-15 years the volume of QTc>0.46, for men>16 years greater than 0.45, and females QTc>0.46 [9, 41, 42]. We here aimed at assessing the effects of KCNQ1 and KCNH2 gene expression level on the occurrence of long QT interval syndrome. To our knowledge, this is the first study that examines KCNQ1 and HERG gene expression in human patients. The rather unique character of this study results from comparing the expression levels of KCNQ1 and KCNH2 genes in subjects with clinically diagnosed LQT1 and LQT2 syndromes and in healthy subjects. The present study is also the first to use patients’ peripheral blood as the material for the subject investigation. Studies on KCNQ1 and HERG expression reported so far were based on animal biopsy material or commercially available cell lines. We have found significantly lower KCNQ1 and KCNH2 mRNA levels in healthy females than in healthy males and significantly lower KCNQ1 and KCNH2 mRNA levels in male patients compared with female patients. These findings suggest that the higher male risk related to acquired cardiovascular disorders in the unaffected population is counterbalanced in the affected population by higher female risk related to the genetic disorder [43]. Previous studies have suggested that the rate of increase in cardiac events generally plateaus in adult males [4, 9]. Event manifestations specifically in LQT1 and LQT2 patients might be modulated differently by age and gender [9, 44]. Preliminary studies suggest that a pro-arrhythmic response may be genetically determined as a result of mutations or polymorphisms in genes encoding ion channels in heart muscle cells [31]. The incidence of life-threatening events was lower among LQT1 patients compared to the other genotypes, partly because of the high prevalence of silent mutation carriers [QTc, 440 ms]; the risk was higher among LQT2 females vs. males and LQT3 males vs. females [45]. We have also compared KCNQ1 and KCNH2 mRNA copy numbers between healthy adults and healthy children and found significantly higher KCNQ1 and lower KCNH2 mRNA levels in healthy adults compared to healthy children. The risk of arrhythmic complications in patients with long QT syndrome also varies according to sex, age and genotype. In LQT1 syndrome caused by mutation of the KCNQ1 gene, the risk is increased in boys before 15 years of age and in adult females is higher than in men. In the LQT2 syndrome caused by mutation in the HERG gene a preponderance of arrhythmic complications risk in girls could be observed but it is very visible in adult women [4, 9, 10]. Comparative analysis of KCNQ1 and KCNH2 mRNA copy numbers in patients divided into subgroups based on age (adults – age below 55 years and over 55 years; children – age below 15 and over 15) in the present study showed significantly higher KCNQ1 and lower KCNH2 mRNA levels in adult patients (age over 55 years) than in adult patients (age below 55 years). Children are typically affected and more than 50% of the patients have experienced their first episode of syncope or cardiac arrest by the age of 15 years [10, 46, 47]. A few additional findings emphasized high risk for first cardiac events during adolescence, with girls experiencing an increased risk compared with boys, a crossover in risk by sex at approximately age 13 years, and a lower rate of first cardiac events in the adult years than in the younger years [4, 5, 11, 48]. LQT1 children were considered as a low-risk group compared to LQT2 or LQT3 mutation carriers, especially under beta blocker therapy [46, 49]. In 2008 Goldenberg et al. [43] suggested that the subjects who are affected with this cLQTS and survive to age 40 years have a relatively lower risk of experiencing disease-related fatal or near fatal arrhythmic events than their younger counterparts. It is also possible that the increasing prevalence of other forms of cardiac and non-cardiac acquired disease processes may dominate mortality risk in the older age group. In our study adult patients (age over 55 years) presented significantly higher KCNQ1 and lower KCNH2 mRNA levels than paediatric patients (age below 15 years). Gender and age also play significant roles in influencing the clinical course of LQTS in that cardiac events tend to occur more frequently in children, with males having an increased risk of events during pre-adolescence and females having higher event rates in adolescence and beyond [4]. Although many LQTS patients develop symptoms during adolescence, some of them experience the first cardiac event in their adulthood [50]. The mechanism of interaction between KCNQ1 and HERG genes is not simple. It has been reported that KCNQ1 coexpression modulates HERG function by enhancing membrane expression of HERG, and that the 2 proteins co-immunoprecipitate, and colocalize in myocytes. In vivo studies in genetically modified rabbits also support a HERG-KCNQ1 interaction [51]. Trafficking-competent KCNQ1 variably influences the function of HERG long QT alleles. Otherwise the KCNQ1 gene product can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3, and interact with CALM. In turn, HERG transcript variants encoding distinct isoforms have been identified. Isoform 3 has no channel activity by itself, but modulates channel characteristics when associated with isoform 1. It is also reported that KCNQ1 and HERG share unique interactions with KCNE1, 2 and 3 subunits. KCNE1 (IsK or MinK) recapitulates IKs when associated with KCNQ1, whereas it augments the amplitude of an IKr-like current when co-expressed with HERG [52]. Recent studies have led to the discovery of microRNAs (miRNAs) as a new player in cardiac excitability by fine-tuning expression of ion channels, transporters, and cellular proteins, which determines the arrhythmogenicity in many conditions. A single mRNA may regulate the expression of many genes with similar functions and modulate the complex picture of the phenotype or disease activity. The excess may also play a role in the paradoxical increase in target gene expression. It was stated that the following participate in cardiac function of micro RNA: mir-1, mir-133 (arrhythmias), mir-21, mir-195 (cardiac hypertrophy), mir-208 (contractility of the heart muscle) [53–55]. Disorders of epigenetic mechanisms of gene regulation may also be the cause of many monogenic and complex diseases. Epigenetics is one of the fastest growing fields of genetics: studies of variation that is not dependent on the primary DNA sequence and the results from the action of specific regulatory mechanisms (DNA methylation, modification of histone proteins, expression of antisense RNA or RNAi) [56]. As the concept of phenotypic heterogeneity of long QT syndrome was postulated and confirmed, the idea had been looming that modifier genes had to exist. Swartz et al. in 2006 currently making a specific effort towards the identification of modifier genes, not only for the duration of QT interval but also, even more, for the clinical severity of LQTS. This research group has identified a first modifier gene for the severity of LQTS. The practically important conclusion is that common polymorphism can amplify the consequences of rare mutations [57].

However, in the light of the results obtained herein it is suggested that gene expression profiles may be an additional criterion of differential diagnosis of LQTS types. At present this is an experimental method which may be helpful in LQTS diagnosis.

In conclusion, our results support the hypothesis that variations in KCNQ1 and HERG gene expression is influenced by age and gender in human patients with long QT syndrome and in healthy subjects. This research has been restricted to small sample numbers which limits the generalizability of its findings. A replication study for the association between gender and age and expression of the analysed genes needs to be performed.

Acknowledgments

The study was supported by a grant (No. N 404 038 31/2150) from the State Committee of Scientific Research (Poland).

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